US20050267505A9 - Adjustable lancet device and method - Google Patents
Adjustable lancet device and method Download PDFInfo
- Publication number
- US20050267505A9 US20050267505A9 US10/641,101 US64110103A US2005267505A9 US 20050267505 A9 US20050267505 A9 US 20050267505A9 US 64110103 A US64110103 A US 64110103A US 2005267505 A9 US2005267505 A9 US 2005267505A9
- Authority
- US
- United States
- Prior art keywords
- lancet device
- holding member
- lancet
- cam wheel
- projection
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Images
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/15—Devices for taking samples of blood
- A61B5/150007—Details
- A61B5/150206—Construction or design features not otherwise provided for; manufacturing or production; packages; sterilisation of piercing element, piercing device or sampling device
- A61B5/150274—Manufacture or production processes or steps for blood sampling devices
- A61B5/15029—Manufacture or production processes or steps for blood sampling devices for driving devices, i.e. means for driving the piercing element
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/15—Devices for taking samples of blood
- A61B5/150007—Details
- A61B5/150015—Source of blood
- A61B5/150022—Source of blood for capillary blood or interstitial fluid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/15—Devices for taking samples of blood
- A61B5/150007—Details
- A61B5/150175—Adjustment of penetration depth
- A61B5/15019—Depth adjustment mechanism using movable stops located inside the piercing device housing and limiting the travel of the drive mechanism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/15—Devices for taking samples of blood
- A61B5/150007—Details
- A61B5/150374—Details of piercing elements or protective means for preventing accidental injuries by such piercing elements
- A61B5/150381—Design of piercing elements
- A61B5/150412—Pointed piercing elements, e.g. needles, lancets for piercing the skin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/15—Devices for taking samples of blood
- A61B5/150007—Details
- A61B5/150801—Means for facilitating use, e.g. by people with impaired vision; means for indicating when used correctly or incorrectly; means for alarming
- A61B5/150824—Means for facilitating use, e.g. by people with impaired vision; means for indicating when used correctly or incorrectly; means for alarming by visual feedback
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/15—Devices for taking samples of blood
- A61B5/151—Devices specially adapted for taking samples of capillary blood, e.g. by lancets, needles or blades
- A61B5/15101—Details
- A61B5/15103—Piercing procedure
- A61B5/15107—Piercing being assisted by a triggering mechanism
- A61B5/15113—Manually triggered, i.e. the triggering requires a deliberate action by the user such as pressing a drive button
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/15—Devices for taking samples of blood
- A61B5/151—Devices specially adapted for taking samples of capillary blood, e.g. by lancets, needles or blades
- A61B5/15101—Details
- A61B5/15115—Driving means for propelling the piercing element to pierce the skin, e.g. comprising mechanisms based on shape memory alloys, magnetism, solenoids, piezoelectric effect, biased elements, resilient elements, vacuum or compressed fluids
- A61B5/15117—Driving means for propelling the piercing element to pierce the skin, e.g. comprising mechanisms based on shape memory alloys, magnetism, solenoids, piezoelectric effect, biased elements, resilient elements, vacuum or compressed fluids comprising biased elements, resilient elements or a spring, e.g. a helical spring, leaf spring, or elastic strap
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/15—Devices for taking samples of blood
- A61B5/151—Devices specially adapted for taking samples of capillary blood, e.g. by lancets, needles or blades
- A61B5/15101—Details
- A61B5/15126—Means for controlling the lancing movement, e.g. 2D- or 3D-shaped elements, tooth-shaped elements or sliding guides
- A61B5/1513—Means for controlling the lancing movement, e.g. 2D- or 3D-shaped elements, tooth-shaped elements or sliding guides comprising linear sliding guides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/15—Devices for taking samples of blood
- A61B5/151—Devices specially adapted for taking samples of capillary blood, e.g. by lancets, needles or blades
- A61B5/15186—Devices loaded with a single lancet, i.e. a single lancet with or without a casing is loaded into a reusable drive device and then discarded after use; drive devices reloadable for multiple use
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/15—Devices for taking samples of blood
- A61B5/151—Devices specially adapted for taking samples of capillary blood, e.g. by lancets, needles or blades
- A61B5/15186—Devices loaded with a single lancet, i.e. a single lancet with or without a casing is loaded into a reusable drive device and then discarded after use; drive devices reloadable for multiple use
- A61B5/15188—Constructional features of reusable driving devices
- A61B5/1519—Constructional features of reusable driving devices comprising driving means, e.g. a spring, for propelling the piercing unit
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/15—Devices for taking samples of blood
- A61B5/151—Devices specially adapted for taking samples of capillary blood, e.g. by lancets, needles or blades
- A61B5/15186—Devices loaded with a single lancet, i.e. a single lancet with or without a casing is loaded into a reusable drive device and then discarded after use; drive devices reloadable for multiple use
- A61B5/15188—Constructional features of reusable driving devices
- A61B5/15192—Constructional features of reusable driving devices comprising driving means, e.g. a spring, for retracting the lancet unit into the driving device housing
- A61B5/15194—Constructional features of reusable driving devices comprising driving means, e.g. a spring, for retracting the lancet unit into the driving device housing fully automatically retracted, i.e. the retraction does not require a deliberate action by the user, e.g. by terminating the contact with the patient's skin
Definitions
- the invention relates to a lancet device having an adjusting capability, and a method of using a lancet device.
- the invention relates to a lancet device which utilizes an adjustable depth penetration. Lancet devices are used to penetrate and puncture the skin in order to allow the taking of a blood sample for testing. The present device allows the user to control the depth of this penetration by a simple adjustment mechanism.
- Lancet devices are commonly used to prick the skin of the user so that one or more drops of blood may be extracted for testing.
- Some users such as diabetics, for example, may have to test their blood sugar levels several times a day. This may be accomplished by the user using a simple needle. However, this procedure is often problematic for the user since the needle may be difficult to handle. Moreover, controlling the depth of penetration cannot be reliably accomplished without the use of a mechanical device. Additionally, many users simply cannot perform the procedure owing to either a fear of needles or because they lack a steady hand. As a result, lancet devices have been developed which allow the user to more easily and reliably perform this procedure.
- An improved device would allow the user to more easily adjust the depth of penetration and would overcome some of the disadvantages described above.
- the skin thickness can vary slightly from user to user and finger to finger, a need exists for efficiently adapting the depth of penetration.
- an index finger may be more calloused than a middle finger, and the more calloused finger will typically have thicker skin.
- U.S. Pat. No. 4,469,110 to SLAMA discloses a mechanism which adjusts the penetration depth by rotating a threaded sleeve relative to a body.
- the SLAMA device is characterized as a “single bottom” device which employs a threaded design which can be expensive to manufacture.
- such a device may require the user to rotate the threaded sleeve up to 360 degrees and more in order to attain the proper depth setting.
- such a threaded resign is prone to inadvertent setting changes since there is nothing but frictional engagement between the mating threads to maintain the adjustment setting.
- the lancet device has a body portion which encloses a lancet and a lancet firing mechanism.
- the lancet typically has a needle extending therefrom and is caused to move towards the tip of the device by a trigger or firing mechanism.
- the lancet device forces the needle, by virtue of the needle being fixed thereto, out of the device by some distance or depth so that the needle can penetrate the skin of the user.
- the function of this firing mechanism and the lancet body design is disclosed in each of 5,797,942 and 5,908,434.
- a lancet device which can accurately and precisely control the depth of penetration of the needle relative to the surface of the user's skin while also being easy to use. It is also desirable for the user to be able to use and adjust the depth penetrating setting with just one hand and/or with less effort that currently required with existing lancet devices.
- a lancet device that includes a body.
- a trigger is preferably mounted to the body, although it can be operatively associated with the body in any other way.
- a front cover includes a skin engaging end that includes a lancet opening through which a lancet needle extends.
- a holding member is movably mounted within the body and comprises a front end and a rear end. The front end is configured to receive a lancet.
- a stop surface moves with the holding member.
- a cam wheel includes cam surfaces which can be contacted by the stop surface. The cam wheel is configured to rotate at least partially. The cam wheel rotates about an axis that is parallel to an axis running through at least one of the lancet opening and the holding member.
- the lancet device may further comprise a back cap configured to move between a retracted position and an original position.
- the back cap may be configured to move the holding member to a retracted position.
- the back cap may be coupled to a surface that engages the rear end of the holding member.
- the back cap may be coupled to in inner sleeve that includes a surface that engages the rear end of the holding member.
- the inner sleeve may comprise an opening that receives a rear end of the holding member.
- the back cap may be coupled to an inner sleeve that includes a surface that engages projections disposed on the rear end of the holding member.
- the lancet device may further comprise a spring for biasing the back cap towards an original position.
- the lancet device may further comprise a first spring for biasing the holding member towards an extended position and a second spring for biasing the holding member in an opposite direction.
- the first and second springs may be arranged within an axial opening of the holding member.
- the first spring may contact one side of a projection extending inwardly from the body and the second spring may contact another side of the projection.
- the projection may extend into an elongated slot formed in the holding member.
- the lancet device may further comprise an end plug mounted to the rear end of the holding member.
- the first spring may be disposed between the projection and an inner wall surface arranged in the area of the front end of the holding member and the second spring may be disposed between the projection and the end plug.
- the trigger may be movably mounted to the body.
- the front cover may be removably mounted to the body.
- the holding member may comprise a projection that includes the stop surface.
- the holding member may comprise an integrally formed projection that includes the stop surface.
- the front end of the holding member may comprise an opening that is configured to removably receive the lancet.
- the lancet device may further comprise a deflecting member configured to be deflected by the trigger.
- the deflecting member may be coupled to the holding member.
- the deflecting member may comprise a first stop surface or end that contacts a first surface of a holding projection extending inwardly from the body.
- the cam wheel may comprise indicia.
- the cam wheel may be a thumb wheel.
- the cam surfaces of the cam wheel may be arranged on a cam section of the cam wheel.
- the cam section may be disposed on an annular side of the cam disk while an outer circumferential surface of the cam wheel includes the indicia.
- the cam wheel may comprise a centrally disposed opening that is mounted about or around the holding member. The opening in the cam wheel may be large enough to allow the holding member to move within it.
- the opening may comprise a center axis that is generally the same as the axis running through the holding member.
- the cam wheel may rotate about an axis that is generally the same as an axis running through at least one of the lancet opening and the holding member.
- the cam wheel may be disposed between the trigger and a back cap.
- the body may comprise a two piece body.
- the cam wheel may be axially retained between inwardly projecting portions of the body.
- the cam wheel may be disposed between a main projection of the body and a back cap.
- the front cover may be removably mounted to the two piece body.
- the lancet device may further comprise a back cap movably mounted to the two piece body.
- the body may comprise at least one curved side indentation through which the cam wheel protrudes.
- the body may comprise two oppositely arranged curved side indentations.
- the body may comprise a mechanism for viewing indicia of the cam disk.
- the mechanism for viewing indicia of the cam disk may comprise an opening.
- the opening may be a generally rectangular slot.
- the lancet device may further comprise projecting walls for one of axially retaining the cam wheel, whereby the walls allow the cam wheel to rotate within the body while being axially retained therein.
- the invention also provides a method of puncturing a surface of skin using the lancet device described above, wherein the method comprises adjusting a set depth of penetration of the needle by moving the cam wheel to a desired set position, disposing the skin engaging end of the lancet device against a user's skin, and triggering the trigger to cause the lancet needle to penetrate the user's skin, wherein the puncture allows a blood sample to be taken.
- the invention also provides a method of using the lancet device described above, wherein the method comprises at least partially rotating the cam wheel to a desired set position, moving the holding member to a retracted position, maintaining the holding member in the retracted position until the trigger is triggered, disposing the skin engaging end of the lancet device against a user's skin, and triggering the trigger to cause movement of the holding member.
- the invention also provides a lancet device, that includes a body, a trigger, a front cover comprising a skin engaging end that includes a lancet opening through which a lancet needle extends.
- a holding member is movably mounted within the body and comprising a front end a rear end. The front end is configured to receive a lancet.
- a stop projection is coupled to the holding member.
- a cam wheel comprises indicia and cam surfaces which can be contacted by the stop projection. The cam wheel is configured to rotate at least partially. The cam wheel is mounted to rotate about or around the holding member.
- the invention also provides a lancet device comprising a body, a trigger, a front cover comprising a skin engaging end that includes a lancet opening through which a lancet needle extends.
- a holding member is movably mounted within the body and comprising a front end a rear end. The front end is configured to receive a lancet.
- a back cap is configured to move the holding member to a retracted position.
- a stop surface is coupled to the holding member.
- a cam wheel is at least partially arranged within the body. The cam wheel comprises indicia and cam surfaces which can be contacted by the stop projection. The cam wheel is configured to rotate at least partially on an axis that is parallel to an axis of the holding member. The cam wheel protrudes from at least one side wall of the body.
- FIG. 1 shows a side cross-section view of one embodiment of the lancet device.
- the device is shown in the loaded (trigger set) position.
- the lancet is also shown in cross-section;
- FIG. 2 shows a side cross-section view of the embodiment of FIG. 1 .
- the device is shown with the lancet needle moving toward a pre-set depth position after it has been triggered;
- FIG. 3 shows a side cross-section view of the embodiment shown in FIG. 1 .
- the device is shown with the lancet needle at a pre-set depth position;
- FIG. 4 shows a top cross-section view of the embodiment shown in FIG. 1 and in the position shown in FIG. 3 ;
- FIG. 5 shows a side cross-section view of the embodiment shown in FIG. 1 .
- the device is shown in the loaded (trigger set) position after it has been so positioned by retracting the trigger setting mechanism;
- FIG. 6A shows a right side view of the embodiment shown in FIG. 1 ;
- FIG. 6B shows a top view of the embodiment shown in FIG. 6A ;
- FIG. 6C shows a left side view of the embodiment shown in FIG. 6B ;
- FIG. 6D shows a front end view of the front cap of the embodiment shown in FIG. 6C ;
- FIG. 6E shows a front end view of the embodiment shown in FIG. 6B , except that the trigger is not shown;
- FIG. 6F shows a rear end view of the embodiment shown in FIG. 6B ;
- FIG. 7A shows a cross-section view of the right body part of the lancet device shown in FIG. 1 ;
- FIG. 7B shows an inside view of the right body part shown in FIG. 7A ;
- FIG. 7C shows an outside view of the right body part shown in FIG. 7A ;
- FIG. 7D shows a front cross-section view of the left-most sectioning arrows shown in FIG. 7B ;
- FIG. 7E shows a front end view of the right body part shown in FIG. 7C ;
- FIG. 7F shows a rear end view of the right body part shown in FIG. 7A ;
- FIG. 7G shows a rear cross-section view of the right-most sectioning arrows shown in FIG. 7B ;
- FIG. 7H shows a rear cross-section view of the middle sectioning arrows shown in FIG. 7B ;
- FIG. 8A shows an outside view of the left body part of the lancet device shown in FIG. 1 ;
- FIG. 8B shows a cross-section view of the left body part shown in FIG. 8A ;
- FIG. 8C shows a bottom view of the left body part shown in FIG. 8B with inner surfaces shown in hidden lines;
- FIG. 8D shows an inside view of the left body part shown in FIG. 8A ;
- FIG. 8E shows a front end view of the left body part shown in FIG. 8A ;
- FIG. 8F shows a front cross-section view of the left-most sectioning arrows shown in FIG. 8D ;
- FIG. 8G shows a rear end view of the left body part shown in FIG. 8B ;
- FIG. 8H shows a rear cross-section view of the right-most sectioning arrows shown in FIG. 8D ;
- FIG. 8I shows a rear cross-section view of the middle sectioning arrows shown in FIG. 8D ;
- FIG. 9A shows a side cross-section view of the front portion of the holding member used in the lancet device shown in FIG. 1 ;
- FIG. 9B shows a top view of the front portion shown in FIG. 9A ;
- FIG. 9C shows another side cross-section view of the front portion shown in FIG. 9A ;
- FIG. 9D shows a front end view of the front portion shown in FIG. 9A ;
- FIG. 10A shows a side cross-section view of the rear portion of the holding member used in the lancet device shown in FIG. 1 ;
- FIG. 10B shows a bottom view of the rear portion shown in FIG. 10A ;
- FIG. 10C shows a front end view of the rear portion shown in FIG. 10B ;
- FIG. 11A shows a rear view of the cam wheel of the lancet device shown in FIG. 1 ;
- FIG. 11B shows a cross-section view of the cam wheel shown in FIG. 11A ;
- FIG. 11C shows a front view of the cam wheel shown in FIG. 11B ;
- FIG. 11D shows an outside view of the cam wheel shown in FIG. 11B ;
- FIG. 11E shows a rear view of the cam wheel in which the cam surfaces and the indicia can be arranged
- FIG. 12A shows a rear view of the end plug shown in FIG. 1 ;
- FIG. 12B shows a side view of the end plug shown in FIG. 1 ;
- FIG. 12C shows a front view of the end plug shown in FIG. 12B ;
- FIG. 13A shows a side view of the first spring shown in FIG. 1 ;
- FIG. 13B shows an end view of the first spring shown in FIG. 13A ;
- FIG. 14A shows a side view of the second spring shown in FIG. 1 ;
- FIG. 14B shows an end view of the second spring shown in FIG. 14A ;
- FIG. 15A shows a side view of the third spring shown in FIG. 1 ;
- FIG. 15B shows an end view of the third spring shown in FIG. 15A ;
- FIG. 16A shows a top cross-section view of the front cap of the lancet device shown in FIG. 1 ;
- FIG. 16B shows a side cross-section view of the front cap of the lancet device shown in FIG. 1 ;
- FIG. 16C shows a side view of the front cap of the lancet device shown in FIG. 16C ;
- FIG. 16D shows a top view of the front cap shown in FIG. 16A ;
- FIG. 16E shows a front end view of the front cap shown in FIG. 16C ;
- FIG. 17A shows a front end view of the trigger element of the lancet device shown in FIG. 1 ;
- FIG. 17B shows a top view of the trigger element shown in FIG. 17A ;
- FIG. 17C shows a rear view of the trigger element shown in FIG. 17B ;
- FIG. 17D shows a side view of the trigger element shown in FIG. 17B ;
- FIG. 17E shows a bottom view of the trigger element shown in FIG. 17B ;
- FIG. 17F shows a partial enlarged view of a front part of the trigger element shown in FIG. 17D ;
- FIG. 17G shows a partial enlarged view of the textured part of the trigger element shown in FIG. 17B ;
- FIG. 18A shows a top view of the back cover shown in FIG. 1 ;
- FIG. 18B shows a rear view of the back cap shown in FIG. 18A ;
- FIG. 18C shows a side view of the back cap shown in FIG. 18A ;
- FIG. 18D shows a cross-section view of the back cap shown in FIG. 18A ;
- FIG. 18E shows a cross-section view of the back cap shown in FIG. 18C ;
- FIG. 19A shows a cross-section view of the inner sleeve member of the lancet device shown in FIG. 1 ;
- FIG. 19B shows a rear view of the inner sleeve member shown in FIG. 19A ;
- FIG. 19C shows a top cross-section view of the inner sleeve member shown in FIG. 19A .
- FIG. 1 shows a side cross-section view of one embodiment of lancet device (the lancet 10 is also shown in cross-section).
- Lancet device LD has a lancet body made up of a right side body portion 100 and a left side body portion 110 (see FIG. 4 ). These parts 100 and 110 are connected, e.g., using adhesives and/or fasteners and/or welding and/or snap-together holding mechanisms (not shown) to each other when the lancet device LD is initially assembled.
- a holding member 30 / 40 is movably disposed within the body parts 100 , 110 .
- a front cover 20 is removably connected or attached to a front portion of the body parts 100 , 110 .
- the lancet device defines a plane P which is configured to contact (i.e., be positioned against) a user's skin.
- the instant embodiment may utilize an inwardly curved surface plane P beyond which the lancet need can extend.
- a back cap 80 is arranged at a rear portion of the body parts 100 , 110 .
- the back cap 80 has a rear portion that can be gripped by a user and a front portion that slides within the body parts 100 , 110 .
- An inner sleeve 70 is connected (after being slid into the back cap 80 ) to the back cap 80 upon assembly of the lancet device.
- movement of the back cap 80 rearwardly causes the holding member 30 / 40 to retract until it reaches the loaded position shown in FIG. 1 .
- the lancet 10 itself, is conventional and includes a needle. It can be removed and replaced with a new one, as is the case in many prior art lancet devices.
- the front portion 30 of the holding member 30 / 40 includes a lancet holding end which receives the lancet 10 therein.
- the holding member 30 / 40 arrangement preferably has three springs mounted thereto.
- a first spring S 1 which can be made of spring steel, is arranged within the holding member 30 / 40 , just behind the lancet receiving portion.
- the first spring S 1 has a diameter of approximately 6.2 mm, a freelength of approximately 36.7 mm, and a wire size of 0.5 mm.
- This spring S 1 causes (and/or biases) the holding member 30 / 40 to move towards an extended position once a trigger 50 is activated (see FIG. 2 ).
- the trigger 50 includes a portion that is arranged within the body parts 100 / 110 , and is mounted to these body parts 100 , 110 .
- the trigger 50 also has a finger engaging (e.g. push button) portion 50 a that can be pushed and/or deflected into the lancet device.
- the trigger 50 functions as a spring in that it is capable of deflecting inwards (see FIG. 2 ) when force is applied to the finger engaging portion 50 a , and is also capable of returning to a pre-deflection position (see FIGS. 1 and 3 ).
- a second spring S 2 which can be made of spring steel, is also arranged within the holding member 30 / 40 arrangement, but behind the first spring S 1 .
- the second spring S 2 has a diameter of approximately 6.2 mm, a freelength of approximately 25.5 mm, and a wire size of 0.5 mm.
- This spring S 2 causes (and/or biases) the holding member 30 / 40 arrangement to move back towards a retracted position once the lancet 10 reaches the extended position. In this way, the lancet 10 (and holding member 30 / 40 ) is automatically retracted after puncturing the skin of a user.
- a third spring S 3 which can also be made of spring steel, is externally mounted to a rear portion 40 of the holding member arrangement 30 / 40 .
- the third spring S 3 has a diameter of approximately 10.1 mm, a freelength of approximately 13.6 mm, and a wire size of 0.25 mm.
- This spring S 3 causes (and/or biases) the back cap 80 (and attached inner sleeve 70 ) to move inwardly within body parts 100 , 110 .
- a user wishes to place the lancet device LD in the loaded position (see FIG. 1 )
- a user need only move back cap 80 rearwardly (see FIG. 5 ) until the holding member arrangement 30 / 40 reaches the position shown in FIG. 1 .
- spring S 3 causes the back cap 80 to return to the position shown in FIGS. 1-4 .
- the lancet device LD also utilizes a cam wheel 60 to adjust the penetration depth of the lancet needle.
- the cam wheel 60 is preferably mounted within both body parts 100 , 110 so as to be at least partially rotatable in each of two directions.
- the cam wheel 60 can be mounted within the body in any desired manner provided it functions properly in the intended manner.
- retaining walls 100 h , 100 i , 110 h and 110 i are utilized. These will be more fully described with regard to FIGS. 7 and 8 .
- the cam wheel 60 also has a plurality of cam surfaces 60 e 1 - 60 e 8 (see FIG.
- the lancet device LD also utilizes an end plug 90 that ensures that the spring S 2 is retained within the holding member 30 / 40 .
- FIG. 1 shows the lancet device LD with the lancet member 30 / 40 in the loaded position, i.e., ready to move to an extended position when the trigger 50 is pressed.
- the holding member 30 / 40 retains the loaded position of FIG. 1 as a result of engagement between a deflecting member 30 c and shoulders that are formed by projections 100 g and 110 g of the body parts 100 , 110 .
- FIG. 2 shows what happens when the trigger 50 is pressed, i.e., the trigger 50 is caused to be deflected inwardly. That is, the holding member 30 / 40 is released from the loaded position of FIG. 1 , and is caused to move towards plane P.
- the trigger 50 causes the deflecting member 30 c to disengage from the projections 100 g / 110 g of the body parts 100 / 110 . As discussed above, this movement is caused by the expansion (in the direction of the axis of the holding member 30 / 40 ) of first spring S 1 .
- the holding member 30 / 40 continues to move towards the plane P until the stop projection 40 i contacts or engages one of the stop surfaces 60 e 1 - 60 e 8 of the cam wheel 60 .
- the trigger 50 preferably moves back (e.g., automatically) to an un-deflected state shown in FIG. 3 .
- the lancet device LD is then ready to be reloaded, i.e., it can then be placed back into the position shown in FIG. 1 .
- FIG. 3 shows the lancet device LD with the holding member 30 / 40 in one of the pre-set extended positions, i.e., in one of the extended positions that will cause a desired puncture depth in the skin of a user (not shown).
- the distance that the lancet needle projects past plane P is thus determined by rotating the cam wheel 60 until the desired setting is reached.
- This setting causes a particular stop surface (i.e., one of surfaces 60 e 1 - 60 e 8 ) to be placed in the path of the stop projection 40 i .
- the various stop surfaces (e.g., 8 surfaces shown in FIG. 11E ) of the cam wheel 60 thus determine how much the holding member 30 / 40 will move in the extended position relative to the plane P.
- FIG. 3 also shows the needle tip projecting through the opening LO in the front cover 20 and past the plane P. And, as discussed above, the trigger 50 has returned to a non-deflected original position.
- the first spring S 1 is preferably disposed inside the holding member 30 / 40 and between an inner wall 30 g (just behind lancet 10 ) of the front part 30 of the holding member 30 / 40 and a projecting guide member 100 m / 110 m of the right and left body parts 100 , 110 . That is, the first spring S 1 is axially retained between a left side surface of projecting guide member 100 m / 110 m and the inner wall 30 g of the front portion 30 of the holding member 30 / 40 . As a result, the first spring S 1 is caused to be compressed when the holding member 30 / 40 is moved back (i.e., to the right) to a retracted position relative to the body parts 100 , 110 .
- the projecting guide member 100 m / 110 m does not move because it is fixed to the body portions 100 and 110 .
- the projecting guide member 100 m / 110 m can be arranged and/or mounted within the body in any desired manner provided it functions for its intended purpose. It can even be formed only on one of the body parts 100 , 110 .
- the first spring S 1 causes (and/or biases) the holding member 30 / 40 towards an extended position once a trigger 50 (not shown in FIG. 4 ) is activated. As a result, the holding member 30 / 40 cannot be moved back to a retracted position without causing the first spring S 1 to be compressed thereby.
- the second spring S 2 is also preferably sized to slide into an internal opening 40 l of the holding member 30 / 40 . More particularly, the second spring S 2 is disposed inside the holding member 30 / 40 and between an inner wall 90 b of the end plug 90 and the projecting guide member 100 m / 110 m of the body parts 100 , 110 . That is, the second spring S 2 is axially retained between a right side surface of projecting guide member 100 m / 110 m and the inner wall 90 b of the end plug 90 . The second spring S 2 is caused to be compressed when the holding member 30 / 40 is moved forward (i.e., to the left) to an extended position relative to the body parts 100 , 110 .
- the projecting guide member 100 m / 110 m does not move because it is fixed to the body portions 100 , 110 .
- the second spring S 2 causes (and/or biases) the holding member 30 / 40 towards a retracted position once the holding member 30 / 40 reaches the various pre-set extended positions (see e.g., FIG. 3 ).
- the second spring S 2 is compressed when the holding member 30 / 40 is extended by the first spring S 1 .
- Spring S 2 then expands axially to retract the holding member 30 / 40 . In this way, the lancet needle only momentarily projects past the plane P in the extended position before it is caused to retract back in the lancet device by the second spring S 2 .
- the lancet needle only projects past or beyond the plane P for a very brief time (i.e., a fraction of a second when the trigger 50 is pressed) and is otherwise not exposed to a user while the front cover 20 is installed thereon. Accordingly, a user or other innocent bystanders can be protected from being injured unintentionally by an exposed needle.
- the third spring S 3 is preferably sized to slide over a rear end of the rear portion 40 of the holding member 30 / 40 . More particularly, the third spring S 3 is disposed over a rear end of the rear portion 40 and between an inner wall 70 d of the inner sleeve 70 and an annular shoulder 40 e of the rear portion 40 . That is, the third spring S 3 is axially retained between a left side inner surface 70 d of the inner sleeve 70 and the annular shoulder 40 e . As a result, the third spring S 3 is caused to be compressed when the back cap 80 is moved rearward (i.e., to the right as in FIG. 5 ) to an extended position relative to the body parts 100 , 110 .
- the third spring S 3 causes (and/or biases) the back cap 80 towards a retracted position (i.e., sliding back into the lancet device) once a user releases the back cap 80 (compare FIG. 5 to FIG. 1 ).
- the third spring S 3 is compressed when the back cap 80 is pulled backwards (to the right in FIG. 5 ) to cause the deflecting member 30 c to seat onto the projections 100 g/ 110 g (adjacent the trigger 50 ) of the body parts 100 , 110 .
- the third spring S 3 then expands axially to cause the back cap 80 to move to the left until shoulders 80 c of the back cap 80 contact end edges 100 b , 110 b of the body parts 100 , 110 .
- the spring S 3 does not compress completely when the back cap 80 is extended (moved to the right). This is because the left side inner surface 70 d of inner sleeve 70 contacts surfaces 40 j 1 and 40 k 1 two oppositely arranged projections 40 j and 40 k of the rear portion 40 of the holding member 30 / 40 .
- FIG. 5 shows another cross-section side view of the lancet device LD shown in FIG. 1 .
- the back cap 80 is shown in the extended position. As described above, this movement is used to retract the holding member 30 / 40 until the deflecting member 30 c engages the projections 100 g / 110 g of the body parts 100 , 110 . At this point, the user need only release the back cap 80 so that the third spring S 3 will automatically cause the back cap 80 to move or retract towards the lancet device until it assumes the position shown in FIG. 1 . As can be seen when comparing FIGS.
- the first spring S 1 becomes compressed axially when the back cap 80 causes the holding member 30 / 40 to move to a retracted position (to the right).
- the second spring S 2 expands axially (compare FIGS. 2 and 5 ), while the third spring S 3 compresses axially (see FIG. 5 ).
- the third spring S 3 expands axially—which causes the back cap 80 (and the attached inner sleeve 70 ) to retract back into the lancet device (see FIG. 1 ).
- FIGS. 6 A-F show right side, top, left, front and rear views of the lancet device LD shown in FIGS. 1-5 .
- the lancet device has a lancet body made up of a right body portion 100 and a left body portion 110 . These parts 100 and 110 are connected to each other when the lancet device is initially assembled.
- a seam line SL is preferably formed and/or provided between the edges 100 a / 110 a and 100 b / 110 b of the body parts 100 , 110 .
- the front cover 20 is preferably removably connected or attached to a front portion of the body parts 100 , 110 . As is shown in FIGS.
- the curved surface plane P has a lancet opening LO through which the lancet needle passes.
- the back cap 80 is arranged at a rear portion of the body parts 100 , 110 .
- the back cap 80 preferably has a rear portion with textured portions 80 q and 80 n (i.e., on each side of the back cap 80 ). These textured portions allow a user to more easily grip the back cap 80 .
- movement of back cap 80 rearwardly causes the holding member 30 / 40 to retract until it reaches the loaded position shown in FIG. 1 .
- the trigger 50 preferably has a tear-drop shaped button 50 a which can be pressed by a user to cause the lancet 10 to move to the extended position.
- the cam wheel 60 can be seen to project partially from a recessed portion 110 n of the left body part 110 .
- the recess 110 n preferably has an inwardly curved surface whose radius is greater than a radius of the cam wheel 60 .
- the left body part 110 has a window W (e.g., a through opening or slot 110 p ) through which one can read the indicia (e.g., numbers or other desired indicia such as letters or marks) of the cam wheel 60 .
- the lancet device LD is configured with curved surfaces 100 q , 110 q and an ergonomic shape to enable a user to grip the device more securely, while also being able to rotate the cam wheel 60 with one or more fingers of the same hand.
- some users may require two hands to place the lancet device in the loaded position, since they may not be able to pull the back cap 80 backwards without using both hands.
- the front cover 20 has circular or curved upper and lower edges 20 b (see also FIG. 16 ) and complex profile side edges 20 a .
- the right and left body parts 100 , 110 have top, side and bottom edges which are shaped to correspond to the circular or curved upper side and lower edges of the front cover 20 .
- the back cap 80 has straight upper, lower and side shoulder edges 80 c (see also FIG. 18 ).
- the right and left body parts 100 , 110 preferably have rear top, bottom and side straight edges 100 b / 110 b which are shaped to correspond to the straight shoulder edges 80 c of the back cap 80 .
- the external surfaces of both the back cap 80 and the front cover 20 have a shape, arrangement and/or configuration which continues the curved and/or tapered external surfaces of the right and left body parts 100 , 110 .
- FIGS. 7 A-H show various views of the right body part 100 .
- the right body part 100 can preferably be made as one-piece structure by e.g., injection molding. In this regard, it is preferably made of a plastic or synthetic resin such as, e.g., ABS plastic.
- the body part 100 may also be made of ABS—Metallic Silver and have a finish designated as SPI-A2. Additionally, the body part 100 may have an overall length that is approximately 3.04′′ (i.e., between edges 100 a and 100 b ). This will ensure that the assembled lancet device can have an overall length of approximately 4.1′′. Of course, other materials and/or finishes may be utilized, without leaving the scope of the invention.
- the body part 100 may even be made of a plurality of sections of parts which are joined together to form the complete body part 100 , without leaving the scope of the invention.
- the right body part 100 preferably has a curved front edge 100 a and curved sides 100 a 1 .
- the radius of this edge 100 a may be approximately 0.38′′.
- the front edge 100 a is configured to abut curved edges 20 a .
- curved side edges 100 a 1 of body part 100 similarly abuts curved edges 20 b of front cap 20 .
- Recesses or indentations 100 a 2 are disposed between front edge 100 a and a projecting shoulder or wall 100 a 3 .
- the recesses 100 a 2 are arranged or configured to receive within it or otherwise engage with a projection 20 c (see FIG. 16C ) of front cap 20 .
- the projections 20 c similarly have rounded portions that corresponds to the rounded bottom of recesses 100 a 2 .
- the recess 100 a 2 may be continuous, or it need not extend continuous from side 100 c to side 100 d . It can instead be formed as intermitted recesses or it may have the form of a single short recess that is arranged only on inner surfaces of sides 100 c and 100 d .
- the body part 100 can have the projection while the front cap 20 has the recess.
- other connecting mechanisms may also be utilized in place of the projection and recess connection.
- the body part 100 also has a curved upper surface US.
- This surface US extends from front edge 100 a to rear edge 100 b , and may have a radius of approximately 30′′ (or may be essentially straight).
- a tear-drop shaped through opening 100 f is arranged within the curved side 100 c (note that the full opening is defined by partial opening 100 f and partial opening 110 f when the two body parts are connected).
- This partial opening 100 f is sized and configured to receive the push button portion 50 a of the trigger 50 (see FIG. 17 ).
- the opening 100 f can have any desired size, shape or configuration provided it allows a user access to the trigger 50 and/or provided that it generally corresponds to the size, shape and configuration of the trigger 50 .
- the opening 100 f is formed in the upper wall 100 c near an inwardly projecting shoulder 100 g .
- this shoulder 100 g is sized, shaped and/or configured to be engaged by the deflecting member 30 c (see FIG. 9 ).
- the projection 100 g has a straight contact surface that is generally parallel to edge 100 b and a bottom surface or edge that can range from being generally perpendicular to edge 100 b , to being tapered or angled by as much as 15 degrees or more.
- the straight contact surface of projection shoulder 100 g is configured to be engaged by surface 30 c 1 of deflecting member 30 c.
- the upper body part 100 additionally preferably includes two plate-like projections or walls 100 h and 100 i which connect sides 100 c and 100 d to side 100 e .
- the purpose of these projections 100 h and 100 i is to axially retain cam wheel 60 .
- These projections 100 h and 100 i have inwardly curved edges 100 h 1 and 100 i 1 .
- the projections 100 h and 100 i are spaced apart by a distance that is slightly greater than a width “w 1 ”of cam wheel 60 (see FIG. 11B ).
- the width “w 1 ” between inner surfaces of projections 100 h and 100 i should be slightly greater than approximately 0.16′′ to accommodate width w 1 of cam wheel 60 being approximately 0.16′′.
- a C-shaped projection 100 j (similar to projection 110 j of FIG. 8D ) also extends inwardly from the wall 100 c (similar to wall 110 c ) of the body part 100 (similar to body part 110 ).
- the projection 100 j forms a right half portion of a bearing system for the trigger 50 .
- the parts 100 j and 110 j form two circular bearing supports for the trigger 50 . As will be described later on with regard to FIG.
- the journal elements 50 c of the trigger 50 are mounted to the bearing supports 100 j / 110 j .
- the body part 100 also preferably includes a connecting rib 100 k that provides strength to the body part 100 and serves to guide holding member 30 / 40 .
- a circular or curved recess 100 k 1 is formed in the center of the rib 100 k .
- This recess 100 k 1 of the rib 100 k can have a radius of approximately 0.17′′.
- the right body part 100 further preferably includes a curved indentation 1001 disposed on side 100 d .
- the radius of indentation 1001 can be approximately 1.76′′.
- a main projection 100 m extends inwardly from body portion 100 .
- the projection 100 m has an internal opening and polygonal outer shape (i.e., square). The purpose of this projection is to guide the holding member 30 / 40 and to prevent it from rotating when it moves axially. It this regard, the projection 100 m (together with projection 110 m ) is sized to fit within slot 40 f of the rear portion of holding member 30 / 40 .
- a pawl member 100 p extends inwardly from body part 100 .
- the pawl member 100 p has a rounded projecting portion that engages a ratchet surface, i.e., undulating surfaces 60 b 1 (notches) and 60 b 2 (projections), of the cam wheel 60 .
- the pawl 100 p deflects towards and away from cam wheel 60 as the cam wheel 60 rotates. In this way, the cam wheel 60 is locked and/or temporarily retained at a desired set-depth position.
- the interaction between pawl 100 p and cam wheel 60 can produce a sound such as, e.g., clicking, when the cam wheel 60 is rotated.
- the body part 100 includes an outward projecting portion 100 n .
- the body part 100 also includes an inwardly curved finger engaging section 100 q which may have a radius of approximately 0.82°.
- the sides 100 c and 100 d can be planar or slightly curved outwardly (i.e., convex).
- the sides 100 c and 100 d can also preferably be curved or tapered outwardly in the width direction (i.e., see FIGS. 7G and H) and may be angled at an angle “a” of approximately 7 degrees (see FIG. 7F ).
- the corners 100 s where the side walls 100 c and 100 d meet wall 100 e can be rounded and have a radius of approximately 0.1′′.
- the rear edge 100 b of the body part 100 is a continuous straight edge that is configured to make contact with shoulder 80 c of back cap 80 (see FIG. 18 ).
- FIGS. 8 A-I show various views of the left body part 110 .
- the body part 110 can preferably be made as one-piece structure by e.g., injection molding. In this regard, it is preferably made of a plastic or synthetic resin such as, e.g., ABS plastic.
- the body part 110 may also have be made of ABS—Metallic Silver and have a finish designated as SPI-A2. Additionally, the body part 110 may have an overall length that is approximately 3.04′′ (i.e., between edges 110 a and 110 b ). This will ensure that the assembled lancet device can have an overall length of approximately 4.1′′.
- other materials and/or finishes may be utilized, without leaving the scope of the invention.
- the body part 110 may even be made of a plurality of sections of parts which are joined together to form the complete body part 110 , without leaving the scope of the invention.
- the body part 110 preferably has a front curved edge 110 a and includes circular and/or curved side edges 110 a 1 .
- the radius of curved edge 110 a may be approximately 0.38′′.
- the front edge 110 a is configured to abut a curved edge 20 a of front cap 20 until contact occurs between circular and/or curved edge 20 a and edge 110 a .
- a recess 110 a 2 is disposed between front edge 110 a and connecting wall 110 a 3 . This recess 110 a 2 is arranged on each of sides 110 c , 110 d , and possibly on side 110 e .
- the projections 20 c similarly has a rounded edge that generally corresponds to the rounded bottom of recesses 110 a 2 .
- the recess 110 a 2 can be either a partial recess or a continuous one, i.e., it can extend continuously from side 110 c to side 110 d .
- it can instead be formed as intermitted recesses or it may have the form of a single short recess that is centrally arranged with respect to walls 110 c and 100 c and walls 100 d and 110 d (when the body parts 100 and 110 are assembled together).
- the body part 110 can have the projection while the front cap 20 has the recess.
- other connecting mechanisms may also be utilized in place of the projection and recess connection.
- the body part 110 also preferably has a curved lower surface LS.
- An inwardly curved surface 110 l is also provided which may have a radius of approximately 1.76′′.
- the lower body part 110 additionally preferably includes two plate-like projections or walls 110 h and 110 i which are generally arranged to connect sides 110 c and 110 d .
- the purpose of these projections 110 h and 110 i is to axially retain the cam wheel 60 in the same way described above with regard to walls 100 h and 100 i .
- the projections 110 h and 110 i are spaced apart a distance similar to projections 100 h and 100 i described with respect to FIG. 7 .
- projections 110 h and 110 i also similarly have inwardly curved recesses of different sizes which allow portions of the cam wheel 60 to axially project therethrough (see e.g., FIG. 1 ).
- walls 100 h and 110 h are generally aligned with one another and have inwardly curved recesses that serve as a bearing for surface 60 c .
- walls 100 i and 110 i are generally aligned with one another and have inwardly curved recesses that serve as a bearing for surface 60 i .
- a C-shaped projection 110 j extends from wall 110 c of the body part 110 in the same way as projection 100 j of body part 100 (but oppositely arranged therefrom).
- This projection 110 j forms the other half of a bearing system for the trigger 50 . Together with the projection 100 j (see FIG. 7 ), i.e., right half of the bearing system, the parts 100 j and 110 j form two circular bearing supports for the trigger 50 . As will be described later on with regard to FIG. 17 , the journal elements 50 c of the trigger 50 are mounted to or within the bearing supports formed by parts 100 j / 110 j .
- the body part 110 additionally includes connecting ribs 110 a 3 and 110 k that provides strength to the body part 110 and act to axially guide the holding member 30 / 40 .
- circular or curved recesses are formed in the center of the ribs 110 a 3 and 110 k .
- These recesses of the ribs 110 a 3 and 110 k can have a radius of approximately 0.17′′.
- the body part 110 further preferably includes a polygonal or square shaped main projection 110 m that is generally centrally disposed relative to sides 110 c and 110 d .
- the purpose of this projection 110 m is to axially and/or non-rotatably guide the holding member 30 / 40 within the lancet device and to serve as stop surfaces for springs S 1 and S 2 (see e.g., FIG. 1 ).
- the projection 110 m has a polygonal (i.e., four sided or square) shaped outer surface. A left side surface of the projection 110 m serves a contact or engage right end of spring S 1 (see e.g., FIG. 1 ).
- a right side surface of the projection 110 m serves a contact or engage left end of spring S 2 (see e.g., FIG. 1 ).
- the projection 110 m also has an inner recess or blind opening. This opening is mainly for ease of manufacture and to reduce material costs.
- the length of the projection 110 m is sized to abut projection 100 m of body part 100 when body parts 100 and 110 are assembled together. Of course, there may be some clearance between projections 100 m and 110 m when the body parts 100 and 110 are assembled together. However, each projection 100 m and 110 m should be of sufficient length so as to project at least partially into the slot 40 f of the back portion 40 of holding member 30 / 40 .
- the body part 110 also preferably includes circular or curved indented side portions 110 q and 110 n .
- Recess 110 q may have a radius of approximately 0.82′′.
- Recess 110 n may have a radius that is greater than approximately 1′′.
- recessed portion 110 n allows a user to access the cam wheel 60 . That way, the user can use a finger to rotate the cam wheel 60 from side 110 e .
- the sides 110 c and 110 d can be angled with an angle “a” of approximately 7 degrees.
- the sides 110 c and 110 d can also have outer surfaces US and LS which are curved outwardly in the length direction (i.e., see FIG.
- the corners 110 s where the side walls 110 c and 110 d meet wall 110 e can be rounded and have a radius of approximately 0.1′′.
- the rear edge 110 b of the body part 110 is preferably a continuous straight edge that is configured to make contact with shoulder 80 c of back cap 80 (see FIG. 18 ).
- surface 110 c extends from front edge 110 a to rear edge 110 b , and may have a radius of approximately 30′′. Alternatively, it may be essentially straight.
- a tear-drop shaped through opening 110 f is arranged within the curved side 110 c (note that the full opening is defined by partial opening 100 f and partial opening 110 f when the two body parts are connected).
- This opening 110 f is sized and configured to receive the push button portion 50 a of the trigger 50 (see FIG. 17 ).
- the opening 110 f can have any desired size, shape or configuration provided it allows a user access to the trigger 50 and provided that it generally corresponds to the size, shape and configuration of the trigger 50 .
- the opening 110 f is formed in the upper wall 110 c near an inwardly projecting shoulder 110 g .
- this shoulder 110 g (as with shoulder 100 g ) is sized, shaped and/or configured to be engaged by the deflecting member 30 c (see FIG. 9 ).
- the projection 110 g has a straight contact surface that is generally parallel to edge 110 b and a bottom surface or edge that can range from being generally perpendicular to edge 110 b to being tapered or angled by as much as 15 degrees or more.
- the straight contact surface of projection shoulder 110 g is configured to be engaged by surface 30 c 1 of deflecting member 30 c.
- FIGS. 9 A-D show various views of the front portion 30 of the two-piece holding member 30 / 40 .
- the front portion 30 can preferably be made as one-piece structure by e.g., injection molding. In this regard, it is preferably made of a plastic or synthetic resin such as, e.g., Delrin plastic.
- the front portion 30 may also be made of Delrin—Natural and have a finish designated as SPI-C1. Additionally, the front portion 30 may have an overall length that is approximately 1.6′′ (i.e., between edges 30 a and 30 b ). Of course, other materials and/or finishes may be utilized, without leaving the scope of the invention.
- the front portion 30 may even be made of a plurality of sections of parts which are joined together to form the complete front portion 30 , without leaving the scope of the invention.
- Front portion 30 preferably has a front end 30 a and a cylindrical section 30 d which may have a diameter of approximately 0.32′′.
- a front opening 30 e is arranged within the cylindrical section 30 d .
- the opening 30 e extends from a wall 30 g to edge 30 a .
- the diameter “d” of the opening 30 e at the edge 30 a may be approximately 0.26′′ and may taper slightly inwards, e.g., by approximately 0.25 degrees (per side), i.e., towards wall 30 g .
- This tapered opening 30 e is sized and configured to securely and/or snugly retain and receive the lancet 10 (see e.g., FIG. 1 ) which may be a conventional lancet.
- Cylindrical section 30 i also has an internal opening 30 j that extends from edge 30 b to shoulder 30 l .
- the opening 30 j is sized and configured to receive end 40 a of rear portion 40 of holding member 30 / 40 (see e.g., FIG. 1 ).
- a deflecting member 30 c preferably extends from cylindrical section 30 i .
- This deflecting member 30 c has a stop surface 30 c 1 which is configured to abut shoulders 100 a 3 and 110 a 3 of the body parts 100 and 110 .
- An upper surface 30 c 2 of the deflecting member 30 c , near end 30 c 1 is designed to be engaged by the trigger 50 (see FIG. 1 ).
- this surface 30 c 2 is configured to be engaged by projection 50 e of the trigger 50 .
- the deflecting member 30 c is capable of deflecting inwards towards the front portion 30 when it is forced inwards towards holding member 30 / 40 .
- Inner diameter 30 j of front portion 30 also preferably includes a continuous rounded recess 30 k which is sized and shaped to receive the continuous rounded projection 40 c of the rear portion 40 .
- the two parts 30 and 40 can be coupled and/or assembled together.
- the projection can be formed on the part 30 and the recess formed on part 40 without leaving the scope of the invention.
- the recess and projection need not be made continuous and can instead be intermittently formed.
- the invention also contemplates other connecting mechanisms besides a projection/recess connection such as, e.g., an adhesive attachment.
- FIGS. 10 A-C show the rear portion 40 of the two-piece holding member 30 / 40 .
- the length between end 40 a and end 40 b can be approximately 1.72′′.
- front end of rear portion 40 has a projection 40 c which engages recess 30 k of the front portion 30 .
- a cylindrical section 40 d extends from projection 40 c to circumferential shoulder 40 e .
- the cylindrical section 40 d may have a diameter of approximately 0.32′′.
- the outer surface may taper or curve inwards to facilitate entry of end 40 a into opening 30 j .
- a through opening 40 l is arranged within the cylindrical section 40 d .
- the opening 40 l extends from end 40 a to end 40 b .
- the diameter of the opening 40 l may be approximately 0.24′′ and, at the edge 40 b , may be approximately 0.244′′ and may taper slightly, e.g., by approximately 0.25 degrees (per side), towards end 40 a .
- This tapered opening section 40 g is sized and configured to securely retain and receive the plug 90 (see e.g., FIG. 1 ).
- the opening 40 l is sized and configured to receive springs S 1 and S 2 (see e.g., FIG. 1 ).
- a recess 40 h is arranged within opening 40 g and is designed to receive projection 90 d of plug 90 (see FIG. 12 ).
- the rounded recess 40 h may be continuous and may be sized and shaped to receive the continuous rounded projection 90 d of the plug 90 .
- the parts 40 and 90 can be coupled and/or assembled together.
- the projection can be formed on the part 40 and the recess formed on part 90 without leaving the scope of the invention.
- the recess and projection need not be made continuous and can instead be intermittently formed.
- the invention also contemplates other connecting mechanisms besides a projection/recess connection such as, e.g., an adhesive attachment.
- End 40 b of the rear part 40 also preferably includes three projections 40 l , 40 j and 40 k .
- Short projections 40 j and 40 k extend in the direction of the axis of the rear portion 40 and are arranged opposite one another, i.e., 180 degrees apart. These projections 40 j and 40 k may have a length of approximately 0.21′′ and a width of approximately 0.05′′.
- Short projections 40 j and 40 k also have stop surfaces 40 j 1 and 40 k 1 . These surfaces 40 j 1 and 40 k 1 are adapted to be engaged and/or contacted by surface 70 d of the inner sleeve 70 when the back cap 80 is moved backwards to load the lancet device (see FIG. 5 ).
- Longer projection 40 i includes a stop shoulder or surface 40 i 1 .
- the stop surface 40 i 1 engages and/or contacts the various cam surfaces 60 e 1 - 60 e 8 of the cam wheel 60 .
- the stop surface 40 i 1 serves to adjust the depth of the lancet needle based upon the position of the cam wheel 60 , as will be described later on.
- the projection 40 i is configured to slide within a recess 70 e of the inner sleeve 70 when the back cap 80 is moved from the positions shown in FIGS. 1 and 5 .
- An elongated through slot 40 f is arranged on the cylindrical section 40 d .
- this slot 40 f is sized and configured to receive projections 100 m and 110 m of the body parts 100 and 110 .
- the width of the slot 40 f can be approximately 0.16′′ while the length SL of the slot 40 f can be approximately 0.74′′.
- the slot 40 f also has rounded ends whose radius SR can be approximately 0.08′′.
- the diameter of shoulder 40 e may be approximately 0.42′′.
- continuous recess or indentation 40 h is sized and configured to receive a projection 90 d of the end plug 90 .
- the recess 40 h may have a radius of approximately 0.007′′ and a depth of approximately 0.004′′.
- diameter 90 c of the end plug 90 is configured to slide into opening 40 g of end 40 b .
- the end plug 90 is secured to the rear portion 40 of holding member 30 / 40 .
- surface 90 b of the end plug 90 serves to engage or contact one end of spring S 2 .
- the end plug 90 is installed once springs S 1 and S 2 are arranged within the openings 30 f and 40 l.
- FIGS. 11 A-E show various views of the cam wheel 60 .
- the cam wheel 60 can preferably be made as one-piece structure by e.g., injection molding. In this regard, it is preferably made of a plastic or synthetic resin such as, e.g., ABS plastic.
- the cam wheel 60 may also have be made of ABS—Dark Blue and have a finish designated as MT-11040. Additionally, the cam wheel 60 may have an overall diameter that is approximately 0.71′′. Of course, other materials and/or finishes may be utilized, without leaving the scope of the invention.
- the cam wheel 60 may even be made of a plurality of sections of parts which are joined together to form the complete cam wheel 60 , without leaving the scope of the invention.
- the cam wheel 60 preferably has an outer circumferential surface 60 e that includes indicia I which may be numbers, e.g., numbers 1-8, or letters. Of course, any desired indicia may be utilized.
- This indicia I can be, e.g., pad printed or silk screen raised numbers in white ink.
- the height of the indicia I can be approximately 0.09′′.
- a centrally disposed opening 60 j extends through the cam disk 60 .
- the opening 60 j may have a diameter of approximately 0.36′′.
- the opening 60 j is sized and configured to rotate around and/or about surface 40 d . Surface 40 d also slides within opening 60 j when holding member 30 / 40 moves within lancet device LD.
- the cam wheel 60 also includes an enlarged diameter opening 60 k that is defined by annular cam surfaces 60 e 1 - 60 e 8 and annular shoulder 60 a .
- the diameter of the cylindrical surface 60 c is sized to rotate (with a clearance) within the circular bearing recess formed by projecting walls 100 h and 110 h .
- the cam wheel 60 includes a plurality of cam surfaces 60 e 1 - 60 e 8 formed on a cam section 60 e . As can be partially seen in FIG. 11B , the cam surfaces 60 e 1 - 60 e 8 are all spaced from edge 60 a by different amounts. As was explained previously, these surfaces 60 e 1 - 8 are configured to be contacted by stop surface 40 i 1 of the holding member 30 / 40 .
- the cam wheel 60 is configured with eight settings (designated by the number of cam surfaces and the indicia), the cam wheel 60 can have any number of desired settings that can range from two to as many as 20 or more, if desired.
- the distance or width “w 1 ” can be approximately 0.16′′ whereas the width “w 2 ” can be approximately 0.33′′.
- a cylindrical recess 60 i is formed between end 60 b and annular surface 60 f .
- the recess surface 60 i is sized to rotate (with a clearance) within the circular bearing recess formed by projecting walls 100 i and 110 i .
- the cam wheel 60 also includes a plurality of angled and/o undulating surfaces 60 b 1 which form pointed tips 60 b 2 . As was explained previously, these surfaces 60 b 1 engage with projection or pawl 100 p and served to temporarily retain the cam wheel 60 in a desired set-depth position.
- a plurality of raised textured portions 60 h are arranged between the indicia I. These allow the user to more easily grip the cam wheel 60 so as to cause its rotation. As was described with regard to FIG. 8 , the cam wheel 60 partially projects through slot 110 p.
- indicia numbers 1-8 can be arranged to correspond to the annular cam surfaces 60 e 1 - 60 e 8 based upon the position of projection 40 i .
- FIG. 11E shows one possible arrangement, it should be noted that the cam surfaces 60 e 1 - 60 e 8 can be arranged in any desired arrangement relative to the indicia and stop projection 40 i , provided that the correct cam surface corresponds to the desired indicia setting.
- FIGS. 12 A-C show various views of the end plug 90 .
- the end plug 90 can preferably be made as one-piece structure by e.g., injection molding. In this regard, it is preferably made of a plastic or synthetic resin such as, e.g., Delrin plastic.
- the end plug 90 may also be made of Delrin—Natural and have a finish designated as SPI-C1. Additionally, the end plug 90 may have an overall length L that is approximately 0.31′′ (i.e., between edges 90 e and 90 b ). Of course, other materials and/or finishes may be utilized, without leaving the scope of the invention.
- the end plug 90 may even be made of a plurality of sections of parts which are joined together to form the complete end plug 90 , without leaving the scope of the invention.
- the end plug 90 preferably has a rear planar wall 90 e and a front planar wall 90 b .
- a shoulder 90 f is arranged between surfaces 90 e and 90 b .
- the diameter of cylindrical surface 90 a can be approximately 0.42′′.
- the diameter of cylindrical surface 90 c can be sized to slide into opening 40 g .
- a projection 90 d extends from surface 90 c and is configured to engage recess 40 h .
- the projection 90 d may have a radius of 0.007′′ and may extend from surface 90 f by approximately 0.004′′.
- End 90 b can also have a chamfer that extends from surface 90 c.
- FIGS. 13 A-B show various views of the plunger spring S 1 .
- the spring S 1 is preferably be made as one-piece structure. In this regard, it is preferably made of 0.05 mm wire.
- the spring S 1 may also have be made of stainless steel 0.05 mm wire. Additionally, the spring S 1 may have an overall freelength of approximately 36.7 mm and an outer diameter of approximately 6.2 mm. In this way, the spring S 1 will be able to move freely within openings 30 f and 40 l .
- other materials may be utilized, without leaving the scope of the invention.
- FIGS. 14 A-B show various views of the return spring S 2 .
- the spring S 2 is preferably be made as one-piece structure. In this regard, it is preferably made of 0.05 mm wire.
- the spring S 2 may also have be made of stainless steel 0.05 mm wire. Additionally, the spring S 2 may have an overall freelength of approximately 25.5 mm and an outer diameter of approximately 6.2 mm. In this way, the spring S 2 will be able to move freely within opening 40 l . Of course, other materials may be utilized, without leaving the scope of the invention.
- FIGS. 15 A-B show various views of the cocking spring S 3 .
- the spring S 3 is preferably be made as one-piece structure. In this regard, it is preferably made of 0.025 mm wire.
- the spring S 3 may also have be made of stainless steel 0.025 mm wire. Additionally, the spring S 3 may have an overall freelength of approximately 13.6 mm and an outer diameter of approximately 10.1 mm. In this way, the spring S 3 will be able to move freely over surface 40 d and projections 40 i , 40 j and 40 k .
- other materials may be utilized, without leaving the scope of the invention.
- FIGS. 16 A-E show various views of the front cover 20 .
- the front cover 20 can preferably be made as one-piece structure by e.g., injection molding. In this regard, it is preferably made of a plastic or synthetic resin such as, e.g., ABS plastic.
- the front cover 20 may also be made of ABS—Light Blue and have a finish designated as SPI-A2. Additionally, the front cover 20 may have an overall length that is approximately 3/4′′ (i.e., between left end of projection 20 c and end 20 f ). Of course, other materials and/or finishes may be utilized, without leaving the scope of the invention.
- the front cover 20 may even be made of a plurality of sections of parts which are joined together to form the complete front cover 20 , without leaving the scope of the invention.
- the front cover 20 preferably has a front wall 20 f that includes a circular and/or curved indentation 20 d (i.e., defining plane P) and a centrally disposed through opening 20 e (i.e., defining lancet opening LO).
- the radius of this indentation 20 d may be approximately 3/8′′ and the diameter of the through opening 20 e may be approximately 0.13′′.
- the invention also contemplates a plane P which is straight or which curves outwardly (not shown).
- the left edges 20 c are configured to slide into front edges 100 a and 110 a until contact occurs between circular and/or curved edges 20 b and edges 100 a 1 and 110 a 1 .
- the projections 20 c may have a radius of approximately 0.02′′. As explained previously, these projections 20 c are configured to engage with the recesses 100 a 2 and 110 a 2 (see FIGS. 7A and 8C ).
- Side walls 20 g and 20 h are preferably tapered inwardly from edge 20 a to surface 20 d and may form rounded corners (e.g., with a radius of approximately 0.1′′) where walls 20 g and 20 h meets wall 20 d .
- Walls 20 g and 20 h can also be curved along their length (see FIG. 16C ), having a radius of approximately 30′′, and may also be curved outwardly (i.e., convex, see FIG. 16C ).
- Side walls 20 g and 20 h may further be formed of tapered surfaces which meet at a center (see FIG. 16E ). These surfaces may tapered outwards from a center at an angle “a” of approximately 7 degrees.
- Rounded corners 20 m are provided between walls 20 g - j .
- the width “w 1 ” of the front cap 20 can be approximately 1/2′′ while the height H 1 can be approximately 0.56′′ (see FIG. 16E ).
- Walls 20 g and 20 h can also include raised and/or textured surfaces 20 k which allow a user to more easily grip the front cap 20 , thus facilitating its removal.
- walls 20 i and 20 j can also include raised and/or textured surfaces 201 which allow a user to more easily grip the front cap 20 .
- the width “w 2 ” of the front cap 20 can be approximately 0.38′′ and can taper inwards by about 1 degree per side towards end 20 d.
- FIGS. 17 A-G show various views of the trigger 50 .
- the trigger 50 can preferably be made as one-piece structure by e.g., injection molding. In this regard, it is preferably made of a plastic or synthetic resin such as, e.g., ABS plastic.
- the trigger 40 may also be made of ABS—Red and have a finish designated as SPI-A2. Additionally, the trigger 50 may have an overall length that is approximately 1.1′′. Of course, other materials and/or finishes may be utilized, without leaving the scope of the invention. Moreover, the trigger 50 may even be made of a plurality of sections of parts which are joined together to form the complete trigger 50 , without leaving the scope of the invention.
- the trigger 50 preferably has a rear end that includes a rounded projection 50 d .
- This rounded projection 50 d is configured to contact an inner surface of body parts 100 and 110 (see FIG. 1 ), and serves to brace or counter the movement of the trigger 50 when the trigger 50 is pressed into the lancet device (See FIG. 2 ).
- the projection 50 d may have a radius of approximately 0.03′′.
- the trigger 50 also has front end 50 b that includes a rounded projection 50 e . This rounded projection 50 e is configured to contact surface 30 c 2 of deflecting member 30 c of the holding member 30 / 40 (see FIG. 9 ) upon movement of the trigger 50 , when the trigger 50 is pressed into the lancet device.
- the projection 50 e may have a radius of approximately 0.03′′.
- the trigger 50 also includes a connecting member 50 g which connects the push button 50 a to the support 50 f .
- Two shaft members or journals 50 c project from opposite sides of the support 50 f .
- the journals 50 c may have a diameter of approximately 0.06′′ and the width “w 1 ” may be 0.36′′.
- These journals 50 c also have rounded ends whose radius can be approximately 0.03′′.
- these journals 50 c are configured to be mounted in the bearing supports formed by projections 100 j and 110 j .
- the openings formed by these projections 100 j and 110 j should be sized to be the same or slightly larger than the diameter of journals 50 c . In this way, the journals 50 c can fit snugly in the supports 100 j / 110 j .
- the width (measured in the direction of FIG. 17E ) of the support 50 f may be approximately 0.1′′.
- the push button 50 a preferably has a tear-drop shape and includes a inwardly curved (i.e., concave) surface that has a radius of approximately 1.9′′.
- a lip member 50 b projects from the front of the push button 50 a .
- This lip member 50 b is approximately 0.06′′ wide and may extend from the push button 50 a by approximately 0.04′′.
- the thickness T 2 of the lip member 50 b (measured in the direction of FIG. 17F ) can be approximately 0.02′′ and the distance T 1 can be approximately 0.04′′.
- Angle “x” can be approximately 5 degrees and angle “y” can be approximately 18 degrees.
- the lip member 50 b limits the upward movement of the push button 50 a by contacting an inner surface of the body parts 100 and 110 when the trigger 50 is in the original non-deflected position (see e.g., FIG. 1 ).
- the push button 50 a can have a width “w 2 ” of approximately 0.25′′.
- the length L 1 can be approximately 0.51′′ while the length L 2 can be approximately 0.57′′.
- the curved surface 50 a can also include a texture (see FIG. 17G ) formed of projections and recesses to prevent a user's finger from slipping off of the button 50 a.
- the trigger 50 is designed to preferably deflect inwardly when a user pushes against the push button 50 a (see FIG. 2 ) and to return to an original position (see FIG. 1 or 3 ).
- the deflection occurs in the area between journals 50 c and connecting element 50 g and/or possibly somewhat between projection 50 d and journals 50 c .
- the design is such that the material properties of the trigger 50 allows it to act like a natural spring.
- FIGS. 18 A-E show various views of the back cap 80 .
- the back cap 80 can preferably be made as one-piece structure by e.g., injection molding. In this regard, it is preferably made of a plastic or synthetic resin such as, e.g., ABS plastic.
- the back cap 80 may also be made of ABS—Light Blue and have a finish designated as SPI-A2. Additionally, the back cap 80 may have an overall length L 2 that is approximately 0.9′′ (i.e., between ends 80 a and 80 b ). Of course, other materials and/or finishes may be utilized, without leaving the scope of the invention.
- the back cap 80 may even be made of a plurality of sections of parts which are joined together to form the complete back cap 80 , without leaving the scope of the invention.
- the back cap 80 preferably has a rear wall 80 b that has a planar outer surface and a planar inner surface 80 d .
- the back cap 80 also has an opening 80 e that extends from end 80 a to surface 80 d .
- This opening 80 e is generally rectangular and has a width “w 1 ” of approximately 0.49′′ and a width “w 2 ” of approximately 0.66′′.
- This opening 80 e extends from edge 80 a and tapers inwardly towards surface 80 d at an angle of approximately 1 degrees (per side).
- the width “w 3 ” between outer surfaces 80 i and 80 h may be approximately 0.53′′ and may taper outwardly from edge 80 a to shoulder 80 c by approximately 1 degree per side.
- the width “w 4 ” between outer surfaces 80 f and 80 g may be approximately 0.72′′ and may taper outwardly from edge 80 a to shoulder 80 c by approximately 1 degree per side.
- the length L 1 from end 80 b to shoulder 80 c may be approximately 0.49′′.
- the walls 80 f - 80 i are configured to slide into rear ends 100 b and 110 b until contact occurs between the shoulder 80 c and edges 100 b and 110 b .
- the back cap 80 and specifically opening 80 e is configured to receive or otherwise engage with the inner sleeve 70 .
- a recess and projection connection may be utilized between the sleeve 70 and back cap 80 .
- other connecting mechanisms may also be utilized in place of the projection and recess connection such as, e.g., a friction fit connection and/or adhesive attachment.
- Side walls 80 j , 80 k , 80 l and 80 m may also taper and/or curve from the top of shoulder 80 c to surface 80 b .
- the approximately square shaped surface 80 b may have a width “w 5 ” of approximately 0.84 and a width “w 6 ” of approximately 0.66′′.
- walls 80 j - 80 m may also have a radius of approximately 1.44′′ and may be outwardly curved, i.e., concave.
- Walls 80 l and 80 m may also have textured surfaces 80 n and the walls 80 j and 80 k may have a textured surface 80 q .
- walls 80 l and 80 m may be formed by tapered surfaces that meet at the center and which have an angle “a” of approximately of 7 degrees.
- FIGS. 19 A-C show various views of the inner sleeve 70 .
- the inner sleeve 70 can preferably be made as one-piece structure by e.g., injection molding. In this regard, it is preferably made of a plastic or synthetic resin such as, e.g., ABS plastic.
- the inner sleeve 70 may also be made of ABS—Light Blue and have a finish designated as SPI-C1. Additionally, the inner sleeve 70 may have an overall length L that is approximately 0.6′′ (i.e., between edges 70 a and 70 b ). Of course, other materials and/or finishes may be utilized, without leaving the scope of the invention.
- the inner sleeve 70 may even be made of a plurality of sections of parts which are joined together to form the complete inner sleeve 70 , without leaving the scope of the invention.
- the inner sleeve 70 has a front wall 70 a that has a planar outer surface and a planar inner surface 70 d .
- An opening 70 c is provided in the wall 70 a .
- This opening 70 c has a circular central part and a generally polygonal recess 70 e .
- Recess 70 e is approximately 0.05′′ wide.
- the recess 70 e is sized and configured to receive projection 40 i .
- the inner sleeve 70 is able slide over the rear portion 40 (from the front) of the holding member 30 / 40 when the lancet device is assembled.
- Surfaces 70 f - 70 i are preferably tapered to match the tapered inner surfaces of opening 80 e . In this way, when the sleeve 70 is inserted into back cap 80 , the shoulder 70 j will abut edge 80 a of the back cap 80 .
- the width “w 1 ” can be approximately 0.42′′.
- the width “w 2 ” can be approximately 0.53′′.
- the width “w 3 ” can be approximately 0.65′′.
- the width “w 4 ” can be approximately 0.72′′.
- the walls 70 h and 70 i can taper from walls 70 f and 70 g by an angle “a” of approximately 7 degrees from a center position (see FIG. 19B ).
- All the parts of the lancet device with the exception of the springs S 1 -S 3 (which can be made of spring steel) and with the exception of the lancet needle (which can be a conventional metal needle mounted to a conventional plastic lancet 10 ), may be made from plastic materials and can be formed using conventional injection molding techniques or other known manufacturing methods.
- the cam disk for example can be integrally formed with peripheral grooves and/or projections (similar to a coin), and with the indicating marks. However, when practical, other materials and manufacturing processes may also be utilized.
Abstract
Description
- 1. Field of the Invention
- The invention relates to a lancet device having an adjusting capability, and a method of using a lancet device. In particular, the invention relates to a lancet device which utilizes an adjustable depth penetration. Lancet devices are used to penetrate and puncture the skin in order to allow the taking of a blood sample for testing. The present device allows the user to control the depth of this penetration by a simple adjustment mechanism.
- 2. Discussion of Background Information
- Lancet devices are commonly used to prick the skin of the user so that one or more drops of blood may be extracted for testing. Some users, such as diabetics, for example, may have to test their blood sugar levels several times a day. This may be accomplished by the user using a simple needle. However, this procedure is often problematic for the user since the needle may be difficult to handle. Moreover, controlling the depth of penetration cannot be reliably accomplished without the use of a mechanical device. Additionally, many users simply cannot perform the procedure owing to either a fear of needles or because they lack a steady hand. As a result, lancet devices have been developed which allow the user to more easily and reliably perform this procedure.
- Most lancet devices lack convenient and flexible adjustability. Such devices are typically made adjustable by switching their tips. U.S. Pat. No. Re. 32,922 to LEVIN et al. is one such device. That is, the user must remove one tip having a set depth and replace it with another having a different set depth. This, of course, creates the problem of storing the replaceable tips, which if not properly done, may result in their misplacement, damage, contamination, or the like.
- An improved device would allow the user to more easily adjust the depth of penetration and would overcome some of the disadvantages described above. Moreover, since the skin thickness can vary slightly from user to user and finger to finger, a need exists for efficiently adapting the depth of penetration. For example, an index finger may be more calloused than a middle finger, and the more calloused finger will typically have thicker skin. By adjusting the depth of puncture so that the depth is no greater than necessary for extracting a required amount of blood, any pain experienced by the user may be minimized.
- Lancets having an adjustable tip are known per se. For example, U.S. Pat. No. 4,469,110 to SLAMA discloses a mechanism which adjusts the penetration depth by rotating a threaded sleeve relative to a body. The SLAMA device is characterized as a “single bottom” device which employs a threaded design which can be expensive to manufacture. Moreover, such a device may require the user to rotate the threaded sleeve up to 360 degrees and more in order to attain the proper depth setting. Further, such a threaded resign is prone to inadvertent setting changes since there is nothing but frictional engagement between the mating threads to maintain the adjustment setting.
- U.S. Pat. No. 4,895,147 to BODICKY et al. functions in a similar manner to the device in SLAMA and therefore suffers from similar disadvantages.
- U.S. Pat. Nos. 5,464,418, 5,797,942, 5,908,434, 6,156,051 and 6,530,937 to SCHRAGA also disclose similar lancet devices and are hereby incorporated herein by reference as though set forth in full herein.
- As disclosed in U.S. Pat. No. 5,908,434, the lancet device has a body portion which encloses a lancet and a lancet firing mechanism. The lancet typically has a needle extending therefrom and is caused to move towards the tip of the device by a trigger or firing mechanism. The lancet device forces the needle, by virtue of the needle being fixed thereto, out of the device by some distance or depth so that the needle can penetrate the skin of the user. The function of this firing mechanism and the lancet body design is disclosed in each of 5,797,942 and 5,908,434. These Patents are incorporated by reference herein in their entirety and are therefore only briefly discussed herein.
- What is needed is a lancet device which can accurately and precisely control the depth of penetration of the needle relative to the surface of the user's skin while also being easy to use. It is also desirable for the user to be able to use and adjust the depth penetrating setting with just one hand and/or with less effort that currently required with existing lancet devices.
- Thus, while advances have been made, there is a continuing need for a lancet device which provides for convenient, reliable and easy adjustment of penetration depth.
- According to one aspect of the invention there is provided a lancet device that includes a body. A trigger is preferably mounted to the body, although it can be operatively associated with the body in any other way. A front cover includes a skin engaging end that includes a lancet opening through which a lancet needle extends. A holding member is movably mounted within the body and comprises a front end and a rear end. The front end is configured to receive a lancet. A stop surface moves with the holding member. A cam wheel includes cam surfaces which can be contacted by the stop surface. The cam wheel is configured to rotate at least partially. The cam wheel rotates about an axis that is parallel to an axis running through at least one of the lancet opening and the holding member.
- The lancet device may further comprise a back cap configured to move between a retracted position and an original position. The back cap may be configured to move the holding member to a retracted position. The back cap may be coupled to a surface that engages the rear end of the holding member. The back cap may be coupled to in inner sleeve that includes a surface that engages the rear end of the holding member. The inner sleeve may comprise an opening that receives a rear end of the holding member. The back cap may be coupled to an inner sleeve that includes a surface that engages projections disposed on the rear end of the holding member.
- The lancet device may further comprise a spring for biasing the back cap towards an original position. The lancet device may further comprise a first spring for biasing the holding member towards an extended position and a second spring for biasing the holding member in an opposite direction. The first and second springs may be arranged within an axial opening of the holding member. The first spring may contact one side of a projection extending inwardly from the body and the second spring may contact another side of the projection. The projection may extend into an elongated slot formed in the holding member.
- The lancet device may further comprise an end plug mounted to the rear end of the holding member. The first spring may be disposed between the projection and an inner wall surface arranged in the area of the front end of the holding member and the second spring may be disposed between the projection and the end plug. The trigger may be movably mounted to the body. The front cover may be removably mounted to the body. The holding member may comprise a projection that includes the stop surface. The holding member may comprise an integrally formed projection that includes the stop surface. The front end of the holding member may comprise an opening that is configured to removably receive the lancet.
- The lancet device may further comprise a deflecting member configured to be deflected by the trigger. The deflecting member may be coupled to the holding member. The deflecting member may comprise a first stop surface or end that contacts a first surface of a holding projection extending inwardly from the body. The cam wheel may comprise indicia. The cam wheel may be a thumb wheel. The cam surfaces of the cam wheel may be arranged on a cam section of the cam wheel. The cam section may be disposed on an annular side of the cam disk while an outer circumferential surface of the cam wheel includes the indicia. The cam wheel may comprise a centrally disposed opening that is mounted about or around the holding member. The opening in the cam wheel may be large enough to allow the holding member to move within it. The opening may comprise a center axis that is generally the same as the axis running through the holding member. The cam wheel may rotate about an axis that is generally the same as an axis running through at least one of the lancet opening and the holding member. The cam wheel may be disposed between the trigger and a back cap. The body may comprise a two piece body. The cam wheel may be axially retained between inwardly projecting portions of the body. The cam wheel may be disposed between a main projection of the body and a back cap. The front cover may be removably mounted to the two piece body. The lancet device may further comprise a back cap movably mounted to the two piece body. The body may comprise at least one curved side indentation through which the cam wheel protrudes. The body may comprise two oppositely arranged curved side indentations. The body may comprise a mechanism for viewing indicia of the cam disk. The mechanism for viewing indicia of the cam disk may comprise an opening. The opening may be a generally rectangular slot. The lancet device may further comprise projecting walls for one of axially retaining the cam wheel, whereby the walls allow the cam wheel to rotate within the body while being axially retained therein.
- The invention also provides a method of puncturing a surface of skin using the lancet device described above, wherein the method comprises adjusting a set depth of penetration of the needle by moving the cam wheel to a desired set position, disposing the skin engaging end of the lancet device against a user's skin, and triggering the trigger to cause the lancet needle to penetrate the user's skin, wherein the puncture allows a blood sample to be taken.
- The invention also provides a method of using the lancet device described above, wherein the method comprises at least partially rotating the cam wheel to a desired set position, moving the holding member to a retracted position, maintaining the holding member in the retracted position until the trigger is triggered, disposing the skin engaging end of the lancet device against a user's skin, and triggering the trigger to cause movement of the holding member.
- The invention also provides a lancet device, that includes a body, a trigger, a front cover comprising a skin engaging end that includes a lancet opening through which a lancet needle extends. A holding member is movably mounted within the body and comprising a front end a rear end. The front end is configured to receive a lancet. A stop projection is coupled to the holding member. A cam wheel comprises indicia and cam surfaces which can be contacted by the stop projection. The cam wheel is configured to rotate at least partially. The cam wheel is mounted to rotate about or around the holding member.
- The invention also provides a lancet device comprising a body, a trigger, a front cover comprising a skin engaging end that includes a lancet opening through which a lancet needle extends. A holding member is movably mounted within the body and comprising a front end a rear end. The front end is configured to receive a lancet. A back cap is configured to move the holding member to a retracted position. A stop surface is coupled to the holding member. A cam wheel is at least partially arranged within the body. The cam wheel comprises indicia and cam surfaces which can be contacted by the stop projection. The cam wheel is configured to rotate at least partially on an axis that is parallel to an axis of the holding member. The cam wheel protrudes from at least one side wall of the body.
- Other exemplary embodiments and advantages of the present invention may be ascertained by reviewing the present disclosure and the accompanying drawing.
- The present invention is further described in the detailed description which follows, in reference to the noted plurality of drawings by way of non-limiting examples of exemplary embodiments of the present invention, in which like reference numerals represent similar parts throughout the several views of the drawings, and wherein:
-
FIG. 1 shows a side cross-section view of one embodiment of the lancet device. The device is shown in the loaded (trigger set) position. The lancet is also shown in cross-section; -
FIG. 2 shows a side cross-section view of the embodiment ofFIG. 1 . The device is shown with the lancet needle moving toward a pre-set depth position after it has been triggered; -
FIG. 3 shows a side cross-section view of the embodiment shown inFIG. 1 . The device is shown with the lancet needle at a pre-set depth position; -
FIG. 4 shows a top cross-section view of the embodiment shown inFIG. 1 and in the position shown inFIG. 3 ; -
FIG. 5 shows a side cross-section view of the embodiment shown inFIG. 1 . The device is shown in the loaded (trigger set) position after it has been so positioned by retracting the trigger setting mechanism; -
FIG. 6A shows a right side view of the embodiment shown inFIG. 1 ; -
FIG. 6B shows a top view of the embodiment shown inFIG. 6A ; -
FIG. 6C shows a left side view of the embodiment shown inFIG. 6B ; -
FIG. 6D shows a front end view of the front cap of the embodiment shown inFIG. 6C ; -
FIG. 6E shows a front end view of the embodiment shown inFIG. 6B , except that the trigger is not shown; -
FIG. 6F shows a rear end view of the embodiment shown inFIG. 6B ; -
FIG. 7A shows a cross-section view of the right body part of the lancet device shown inFIG. 1 ; -
FIG. 7B shows an inside view of the right body part shown inFIG. 7A ; -
FIG. 7C shows an outside view of the right body part shown inFIG. 7A ; -
FIG. 7D shows a front cross-section view of the left-most sectioning arrows shown inFIG. 7B ; -
FIG. 7E shows a front end view of the right body part shown inFIG. 7C ; -
FIG. 7F shows a rear end view of the right body part shown inFIG. 7A ; -
FIG. 7G shows a rear cross-section view of the right-most sectioning arrows shown inFIG. 7B ; -
FIG. 7H shows a rear cross-section view of the middle sectioning arrows shown inFIG. 7B ; -
FIG. 8A shows an outside view of the left body part of the lancet device shown inFIG. 1 ; -
FIG. 8B shows a cross-section view of the left body part shown inFIG. 8A ; -
FIG. 8C shows a bottom view of the left body part shown inFIG. 8B with inner surfaces shown in hidden lines; -
FIG. 8D shows an inside view of the left body part shown inFIG. 8A ; -
FIG. 8E shows a front end view of the left body part shown inFIG. 8A ; -
FIG. 8F shows a front cross-section view of the left-most sectioning arrows shown inFIG. 8D ; -
FIG. 8G shows a rear end view of the left body part shown inFIG. 8B ; -
FIG. 8H shows a rear cross-section view of the right-most sectioning arrows shown inFIG. 8D ; -
FIG. 8I shows a rear cross-section view of the middle sectioning arrows shown inFIG. 8D ; -
FIG. 9A shows a side cross-section view of the front portion of the holding member used in the lancet device shown inFIG. 1 ; -
FIG. 9B shows a top view of the front portion shown inFIG. 9A ; -
FIG. 9C shows another side cross-section view of the front portion shown inFIG. 9A ; -
FIG. 9D shows a front end view of the front portion shown inFIG. 9A ; -
FIG. 10A shows a side cross-section view of the rear portion of the holding member used in the lancet device shown inFIG. 1 ; -
FIG. 10B shows a bottom view of the rear portion shown inFIG. 10A ; -
FIG. 10C shows a front end view of the rear portion shown inFIG. 10B ; -
FIG. 11A shows a rear view of the cam wheel of the lancet device shown inFIG. 1 ; -
FIG. 11B shows a cross-section view of the cam wheel shown inFIG. 11A ; -
FIG. 11C shows a front view of the cam wheel shown inFIG. 11B ; -
FIG. 11D shows an outside view of the cam wheel shown inFIG. 11B ; -
FIG. 11E shows a rear view of the cam wheel in which the cam surfaces and the indicia can be arranged; -
FIG. 12A shows a rear view of the end plug shown inFIG. 1 ; -
FIG. 12B shows a side view of the end plug shown inFIG. 1 ; -
FIG. 12C shows a front view of the end plug shown inFIG. 12B ; -
FIG. 13A shows a side view of the first spring shown inFIG. 1 ; -
FIG. 13B shows an end view of the first spring shown inFIG. 13A ; -
FIG. 14A shows a side view of the second spring shown inFIG. 1 ; -
FIG. 14B shows an end view of the second spring shown inFIG. 14A ; -
FIG. 15A shows a side view of the third spring shown inFIG. 1 ; -
FIG. 15B shows an end view of the third spring shown inFIG. 15A ; -
FIG. 16A shows a top cross-section view of the front cap of the lancet device shown inFIG. 1 ; -
FIG. 16B shows a side cross-section view of the front cap of the lancet device shown inFIG. 1 ; -
FIG. 16C shows a side view of the front cap of the lancet device shown inFIG. 16C ; -
FIG. 16D shows a top view of the front cap shown inFIG. 16A ; -
FIG. 16E shows a front end view of the front cap shown inFIG. 16C ; -
FIG. 17A shows a front end view of the trigger element of the lancet device shown inFIG. 1 ; -
FIG. 17B shows a top view of the trigger element shown inFIG. 17A ; -
FIG. 17C shows a rear view of the trigger element shown inFIG. 17B ; -
FIG. 17D shows a side view of the trigger element shown inFIG. 17B ; -
FIG. 17E shows a bottom view of the trigger element shown inFIG. 17B ; -
FIG. 17F shows a partial enlarged view of a front part of the trigger element shown inFIG. 17D ; -
FIG. 17G shows a partial enlarged view of the textured part of the trigger element shown inFIG. 17B ; -
FIG. 18A shows a top view of the back cover shown inFIG. 1 ; -
FIG. 18B shows a rear view of the back cap shown inFIG. 18A ; -
FIG. 18C shows a side view of the back cap shown inFIG. 18A ; -
FIG. 18D shows a cross-section view of the back cap shown inFIG. 18A ; -
FIG. 18E shows a cross-section view of the back cap shown inFIG. 18C ; -
FIG. 19A shows a cross-section view of the inner sleeve member of the lancet device shown inFIG. 1 ; -
FIG. 19B shows a rear view of the inner sleeve member shown inFIG. 19A ; and -
FIG. 19C shows a top cross-section view of the inner sleeve member shown inFIG. 19A . - The particulars shown herein are by way of example and for purposes of illustrative discussion of the embodiments of the present invention only and are presented in the cause of providing what is believed to be the most useful and readily understood description of the principles and conceptual aspects of the present invention. In this regard, no attempt is made to show structural details of the present invention in more detail than is necessary for the fundamental understanding of the present invention, the description taken with the drawings making apparent to those skilled in the art how the several forms of the present invention may be embodied in practice.
-
FIG. 1 shows a side cross-section view of one embodiment of lancet device (thelancet 10 is also shown in cross-section). Lancet device LD has a lancet body made up of a rightside body portion 100 and a left side body portion 110 (seeFIG. 4 ). Theseparts member 30/40 is movably disposed within thebody parts front cover 20 is removably connected or attached to a front portion of thebody parts front cover 20, one can gain access to thelancet 10. Thelancet 10 can thus be removed and replaced with anew lancet 10, as needed, once thefront cover 20 is removed. As in many prior art lancet devices, the lancet device defines a plane P which is configured to contact (i.e., be positioned against) a user's skin. However, unlike known lancet devices, the instant embodiment may utilize an inwardly curved surface plane P beyond which the lancet need can extend. Next, aback cap 80 is arranged at a rear portion of thebody parts back cap 80 has a rear portion that can be gripped by a user and a front portion that slides within thebody parts inner sleeve 70 is connected (after being slid into the back cap 80) to theback cap 80 upon assembly of the lancet device. As will be described in more detail later on, movement of theback cap 80 rearwardly (seeFIG. 5 ), causes the holdingmember 30/40 to retract until it reaches the loaded position shown inFIG. 1 . Thelancet 10, itself, is conventional and includes a needle. It can be removed and replaced with a new one, as is the case in many prior art lancet devices. To ensure thatlancet 10 is securely (yet removably) retained within the lancet device, thefront portion 30 of the holdingmember 30/40 includes a lancet holding end which receives thelancet 10 therein. - As can be seen in
FIG. 1 , the holdingmember 30/40 arrangement preferably has three springs mounted thereto. In this regard, a first spring S1, which can be made of spring steel, is arranged within the holdingmember 30/40, just behind the lancet receiving portion. Preferably, the first spring S1 has a diameter of approximately 6.2 mm, a freelength of approximately 36.7 mm, and a wire size of 0.5 mm. This spring S1 causes (and/or biases) the holdingmember 30/40 to move towards an extended position once atrigger 50 is activated (seeFIG. 2 ). Thetrigger 50 includes a portion that is arranged within thebody parts 100/110, and is mounted to thesebody parts trigger 50 also has a finger engaging (e.g. push button)portion 50 a that can be pushed and/or deflected into the lancet device. Thetrigger 50 functions as a spring in that it is capable of deflecting inwards (seeFIG. 2 ) when force is applied to thefinger engaging portion 50 a, and is also capable of returning to a pre-deflection position (seeFIGS. 1 and 3 ). A second spring S2, which can be made of spring steel, is also arranged within the holdingmember 30/40 arrangement, but behind the first spring S1. Preferably, the second spring S2 has a diameter of approximately 6.2 mm, a freelength of approximately 25.5 mm, and a wire size of 0.5 mm. This spring S2 causes (and/or biases) the holdingmember 30/40 arrangement to move back towards a retracted position once thelancet 10 reaches the extended position. In this way, the lancet 10 (and holdingmember 30/40) is automatically retracted after puncturing the skin of a user. A third spring S3, which can also be made of spring steel, is externally mounted to arear portion 40 of the holdingmember arrangement 30/40. Preferably, the third spring S3 has a diameter of approximately 10.1 mm, a freelength of approximately 13.6 mm, and a wire size of 0.25 mm. This spring S3 causes (and/or biases) the back cap 80 (and attached inner sleeve 70) to move inwardly withinbody parts FIG. 1 ), a user need only move backcap 80 rearwardly (seeFIG. 5 ) until the holdingmember arrangement 30/40 reaches the position shown inFIG. 1 . This, in turn, compresses the third spring S3 to a certain extent. However, when the user releases theback cap 80, spring S3 causes theback cap 80 to return to the position shown inFIGS. 1-4 . - The lancet device LD also utilizes a
cam wheel 60 to adjust the penetration depth of the lancet needle. Thecam wheel 60 is preferably mounted within bothbody parts cam wheel 60 can be mounted within the body in any desired manner provided it functions properly in the intended manner. To ensure that thecam wheel 60 is axially retained tobody parts walls FIGS. 7 and 8 . Thecam wheel 60 also has a plurality of cam surfaces 60 e 1-60 e 8 (seeFIG. 11E ) which are configured to be engaged by astop projection 40 i (inparticular stop surface 40 i 1 ofstop projection 40 i) that is formed on or coupled to therear portion 40 of holdingmember 30/40. Finally, the lancet device LD also utilizes anend plug 90 that ensures that the spring S2 is retained within the holdingmember 30/40. - As described above,
FIG. 1 shows the lancet device LD with thelancet member 30/40 in the loaded position, i.e., ready to move to an extended position when thetrigger 50 is pressed. The holdingmember 30/40 retains the loaded position ofFIG. 1 as a result of engagement between a deflectingmember 30 c and shoulders that are formed byprojections 100 g and 110 g of thebody parts FIG. 2 shows what happens when thetrigger 50 is pressed, i.e., thetrigger 50 is caused to be deflected inwardly. That is, the holdingmember 30/40 is released from the loaded position ofFIG. 1 , and is caused to move towards plane P. This occurs because thetrigger 50 causes the deflectingmember 30 c to disengage from theprojections 100 g/110 g of thebody parts 100/110. As discussed above, this movement is caused by the expansion (in the direction of the axis of the holdingmember 30/40) of first spring S1. The holdingmember 30/40 continues to move towards the plane P until thestop projection 40 i contacts or engages one of the stop surfaces 60 e 1-60e 8 of thecam wheel 60. Once thetrigger 50 is released (once a user stops pressing on the trigger 50), thetrigger 50 preferably moves back (e.g., automatically) to an un-deflected state shown inFIG. 3 . The lancet device LD is then ready to be reloaded, i.e., it can then be placed back into the position shown inFIG. 1 . -
FIG. 3 shows the lancet device LD with the holdingmember 30/40 in one of the pre-set extended positions, i.e., in one of the extended positions that will cause a desired puncture depth in the skin of a user (not shown). The distance that the lancet needle projects past plane P is thus determined by rotating thecam wheel 60 until the desired setting is reached. This setting, in turn, causes a particular stop surface (i.e., one of surfaces 60 e 1-60 e 8) to be placed in the path of thestop projection 40 i. The various stop surfaces (e.g., 8 surfaces shown inFIG. 11E ) of thecam wheel 60 thus determine how much the holdingmember 30/40 will move in the extended position relative to the plane P. The depth setting is thus controlled by contact between thestop projection 40 i and one of the surfaces 60 e 1-60e 8 of the cam wheel 60 (seeFIG. 4 ).FIG. 3 also shows the needle tip projecting through the opening LO in thefront cover 20 and past the plane P. And, as discussed above, thetrigger 50 has returned to a non-deflected original position. -
FIG. 4 shows a top cross-section view of the lancet device ofFIG. 1 . In this regard, the holdingmember 30/40 is in the position shown inFIG. 3 . As inFIGS. 1-3 , thefront cover 20, backcap 80,inner sleeve 70,end plug 90, holdingmember 30/40 andlancet 10 can be seen in their installed and/or assembled position. However, this FIGURE allows one to more clearly see that the first spring S1 is arranged within the holdingmember 30/40, just behind the lancet receiving portion. The first spring S1 is preferably sized to slide intointernal openings 30 f and 40 l of the holdingmember 30/40. More particularly, the first spring S1 is preferably disposed inside the holdingmember 30/40 and between an inner wall 30 g (just behind lancet 10) of thefront part 30 of the holdingmember 30/40 and a projectingguide member 100 m/110 m of the right and leftbody parts guide member 100 m/110 m and the inner wall 30 g of thefront portion 30 of the holdingmember 30/40. As a result, the first spring S1 is caused to be compressed when the holdingmember 30/40 is moved back (i.e., to the right) to a retracted position relative to thebody parts guide member 100 m/110 m does not move because it is fixed to thebody portions guide member 100 m/110 m can be arranged and/or mounted within the body in any desired manner provided it functions for its intended purpose. It can even be formed only on one of thebody parts member 30/40 towards an extended position once a trigger 50 (not shown inFIG. 4 ) is activated. As a result, the holdingmember 30/40 cannot be moved back to a retracted position without causing the first spring S1 to be compressed thereby. - The second spring S2 is also preferably sized to slide into an internal opening 40 l of the holding
member 30/40. More particularly, the second spring S2 is disposed inside the holdingmember 30/40 and between an inner wall 90 b of theend plug 90 and the projectingguide member 100 m/110 m of thebody parts guide member 100 m/110 m and the inner wall 90 b of theend plug 90. The second spring S2 is caused to be compressed when the holdingmember 30/40 is moved forward (i.e., to the left) to an extended position relative to thebody parts guide member 100 m/110 m does not move because it is fixed to thebody portions member 30/40 towards a retracted position once the holdingmember 30/40 reaches the various pre-set extended positions (see e.g.,FIG. 3 ). Thus, the second spring S2 is compressed when the holdingmember 30/40 is extended by the first spring S1. Spring S2 then expands axially to retract the holdingmember 30/40. In this way, the lancet needle only momentarily projects past the plane P in the extended position before it is caused to retract back in the lancet device by the second spring S2. As a result, the lancet needle only projects past or beyond the plane P for a very brief time (i.e., a fraction of a second when thetrigger 50 is pressed) and is otherwise not exposed to a user while thefront cover 20 is installed thereon. Accordingly, a user or other innocent bystanders can be protected from being injured unintentionally by an exposed needle. - The third spring S3 is preferably sized to slide over a rear end of the
rear portion 40 of the holdingmember 30/40. More particularly, the third spring S3 is disposed over a rear end of therear portion 40 and between an inner wall 70 d of theinner sleeve 70 and an annular shoulder 40 e of therear portion 40. That is, the third spring S3 is axially retained between a left side inner surface 70 d of theinner sleeve 70 and the annular shoulder 40 e. As a result, the third spring S3 is caused to be compressed when theback cap 80 is moved rearward (i.e., to the right as inFIG. 5 ) to an extended position relative to thebody parts back cap 80 towards a retracted position (i.e., sliding back into the lancet device) once a user releases the back cap 80 (compareFIG. 5 toFIG. 1 ). Thus, the third spring S3 is compressed when theback cap 80 is pulled backwards (to the right inFIG. 5 ) to cause the deflectingmember 30 c to seat onto theprojections 100 g/ 110 g (adjacent the trigger 50) of thebody parts back cap 80 to move to the left until shoulders 80 c of theback cap 80 contact end edges 100 b, 110 b of thebody parts back cap 80 is extended (moved to the right). This is because the left side inner surface 70 d ofinner sleeve 70 contacts surfaces 40 j 1 and 40 k 1 two oppositely arranged projections 40 j and 40 k of therear portion 40 of the holdingmember 30/40. -
FIG. 5 shows another cross-section side view of the lancet device LD shown inFIG. 1 . InFIG. 5 , theback cap 80 is shown in the extended position. As described above, this movement is used to retract the holdingmember 30/40 until the deflectingmember 30 c engages theprojections 100 g/110 g of thebody parts back cap 80 so that the third spring S3 will automatically cause theback cap 80 to move or retract towards the lancet device until it assumes the position shown inFIG. 1 . As can be seen when comparingFIGS. 2 and 5 , the first spring S1 becomes compressed axially when theback cap 80 causes the holdingmember 30/40 to move to a retracted position (to the right). As a result, the second spring S2 expands axially (compareFIGS. 2 and 5 ), while the third spring S3 compresses axially (seeFIG. 5 ). However, once theback cap 80 is released, the third spring S3 expands axially—which causes the back cap 80 (and the attached inner sleeve 70) to retract back into the lancet device (seeFIG. 1 ). - FIGS. 6A-F show right side, top, left, front and rear views of the lancet device LD shown in
FIGS. 1-5 . As discussed above, the lancet device has a lancet body made up of aright body portion 100 and aleft body portion 110. Theseparts body parts front cover 20 is preferably removably connected or attached to a front portion of thebody parts FIGS. 6B and 6E , the curved surface plane P has a lancet opening LO through which the lancet needle passes. Theback cap 80 is arranged at a rear portion of thebody parts back cap 80 preferably has a rear portion withtextured portions 80 q and 80 n (i.e., on each side of the back cap 80). These textured portions allow a user to more easily grip theback cap 80. As discussed above, movement ofback cap 80 rearwardly (as inFIG. 5 ) causes the holdingmember 30/40 to retract until it reaches the loaded position shown inFIG. 1 . - Again, with reference to FIGS. 6A-F, the
trigger 50 preferably has a tear-drop shapedbutton 50 a which can be pressed by a user to cause thelancet 10 to move to the extended position. Thecam wheel 60 can be seen to project partially from a recessed portion 110 n of theleft body part 110. In this regard, the recess 110 n preferably has an inwardly curved surface whose radius is greater than a radius of thecam wheel 60. In order to allow the user to see which cam surface (one of surfaces 60 e 1-60 e 8) is arranged in the path of thestop projection 40 i (i.e., to adjust the desired depth setting) theleft body part 110 has a window W (e.g., a through opening or slot 110 p) through which one can read the indicia (e.g., numbers or other desired indicia such as letters or marks) of thecam wheel 60. As should be evident, the lancet device LD is configured with curved surfaces 100 q, 110 q and an ergonomic shape to enable a user to grip the device more securely, while also being able to rotate thecam wheel 60 with one or more fingers of the same hand. Unlike the devices of the prior art, one can adjust the depth of penetration without using both hands. Of course, some users may require two hands to place the lancet device in the loaded position, since they may not be able to pull theback cap 80 backwards without using both hands. - To ensure that there is a smooth transition between the various parts of the lancet device, certain edges are preferably made to have a curved and/or profiled arrangement. Thus, the
front cover 20 has circular or curved upper and lower edges 20 b (see alsoFIG. 16 ) and complex profile side edges 20 a. Similarly, the right and leftbody parts front cover 20. Theback cap 80 has straight upper, lower and side shoulder edges 80 c (see alsoFIG. 18 ). Similarly, the right and leftbody parts back cap 80. Additionally, the external surfaces of both theback cap 80 and thefront cover 20 have a shape, arrangement and/or configuration which continues the curved and/or tapered external surfaces of the right and leftbody parts - FIGS. 7A-H show various views of the
right body part 100. Theright body part 100 can preferably be made as one-piece structure by e.g., injection molding. In this regard, it is preferably made of a plastic or synthetic resin such as, e.g., ABS plastic. Thebody part 100 may also be made of ABS—Metallic Silver and have a finish designated as SPI-A2. Additionally, thebody part 100 may have an overall length that is approximately 3.04″ (i.e., between edges 100 a and 100 b). This will ensure that the assembled lancet device can have an overall length of approximately 4.1″. Of course, other materials and/or finishes may be utilized, without leaving the scope of the invention. Moreover, thebody part 100 may even be made of a plurality of sections of parts which are joined together to form thecomplete body part 100, without leaving the scope of the invention. - The
right body part 100 preferably has a curved front edge 100 a and curved sides 100 a 1. The radius of this edge 100 a may be approximately 0.38″. As will be described later on with regard toFIG. 16 , the front edge 100 a is configured to abut curved edges 20 a. Moreover, curved side edges 100 a 1 ofbody part 100 similarly abuts curved edges 20 b offront cap 20. Recesses or indentations 100 a 2 are disposed between front edge 100 a and a projecting shoulder or wall 100 a 3. The recesses 100 a 2 are arranged or configured to receive within it or otherwise engage with a projection 20 c (seeFIG. 16C ) offront cap 20. In this regard, the projections 20 c similarly have rounded portions that corresponds to the rounded bottom of recesses 100 a 2. Of course, the recess 100 a 2 may be continuous, or it need not extend continuous from side 100 c to side 100 d. It can instead be formed as intermitted recesses or it may have the form of a single short recess that is arranged only on inner surfaces of sides 100 c and 100 d. Alternatively, thebody part 100 can have the projection while thefront cap 20 has the recess. Of course, other connecting mechanisms, whether conventional or otherwise, may also be utilized in place of the projection and recess connection. - The
body part 100 also has a curved upper surface US. This surface US extends from front edge 100 a to rear edge 100 b, and may have a radius of approximately 30″ (or may be essentially straight). Arranged within the curved side 100 c is a tear-drop shaped throughopening 100 f (note that the full opening is defined bypartial opening 100 f and partial opening 110 f when the two body parts are connected). Thispartial opening 100 f is sized and configured to receive thepush button portion 50 a of the trigger 50 (seeFIG. 17 ). Of course, theopening 100 f can have any desired size, shape or configuration provided it allows a user access to thetrigger 50 and/or provided that it generally corresponds to the size, shape and configuration of thetrigger 50. Theopening 100 f is formed in the upper wall 100 c near an inwardly projectingshoulder 100 g. As was described previously, thisshoulder 100 g is sized, shaped and/or configured to be engaged by the deflectingmember 30 c (seeFIG. 9 ). In this regard, theprojection 100 g has a straight contact surface that is generally parallel to edge 100 b and a bottom surface or edge that can range from being generally perpendicular to edge 100 b, to being tapered or angled by as much as 15 degrees or more. As will be described later on with regard toFIG. 9 , the straight contact surface ofprojection shoulder 100 g is configured to be engaged bysurface 30 c 1 of deflectingmember 30 c. - The
upper body part 100 additionally preferably includes two plate-like projections orwalls projections cam wheel 60. Theseprojections curved edges 100h 1 and 100 i 1. In this regard, theprojections FIG. 11B ). By ensuring that theprojections cam wheel 60, thecam wheel 60 will be allowed to rotate with ease. In this regard, the width “w1” between inner surfaces ofprojections cam wheel 60 being approximately 0.16″. A C-shaped projection 100 j (similar to projection 110 j ofFIG. 8D ) also extends inwardly from the wall 100 c (similar to wall 110 c) of the body part 100 (similar to body part 110). The projection 100 j forms a right half portion of a bearing system for thetrigger 50. Together with the projection 110 j (seeFIG. 8 ), the parts 100 j and 110 j form two circular bearing supports for thetrigger 50. As will be described later on with regard toFIG. 17 , thejournal elements 50 c of thetrigger 50 are mounted to the bearing supports 100 j/110 j. Thebody part 100 also preferably includes a connecting rib 100 k that provides strength to thebody part 100 and serves to guide holdingmember 30/40. In order to allow the holdingmember 30/40 move freely within the lancet device and without being obstructed by the rib 100 k, a circular or curved recess 100 k 1 (seeFIG. 7D ) is formed in the center of the rib 100 k. This recess 100 k 1 of the rib 100 k can have a radius of approximately 0.17″. - The
right body part 100 further preferably includes acurved indentation 1001 disposed on side 100 d. The radius ofindentation 1001 can be approximately 1.76″. Amain projection 100 m extends inwardly frombody portion 100. Theprojection 100 m has an internal opening and polygonal outer shape (i.e., square). The purpose of this projection is to guide the holdingmember 30/40 and to prevent it from rotating when it moves axially. It this regard, theprojection 100 m (together withprojection 110 m) is sized to fit withinslot 40 f of the rear portion of holdingmember 30/40. Apawl member 100 p extends inwardly frombody part 100. Thepawl member 100 p has a rounded projecting portion that engages a ratchet surface, i.e., undulating surfaces 60 b 1 (notches) and 60 b 2 (projections), of thecam wheel 60. Thepawl 100 p deflects towards and away fromcam wheel 60 as thecam wheel 60 rotates. In this way, thecam wheel 60 is locked and/or temporarily retained at a desired set-depth position. The interaction betweenpawl 100 p andcam wheel 60 can produce a sound such as, e.g., clicking, when thecam wheel 60 is rotated. In order to accommodate thecam wheel 60, thebody part 100 includes an outward projectingportion 100 n. Thebody part 100 also includes an inwardly curved finger engaging section 100 q which may have a radius of approximately 0.82°. - As seen in
FIG. 7C , the sides 100 c and 100 d can be planar or slightly curved outwardly (i.e., convex). The sides 100 c and 100 d can also preferably be curved or tapered outwardly in the width direction (i.e., seeFIGS. 7G and H) and may be angled at an angle “a” of approximately 7 degrees (seeFIG. 7F ). The corners 100 s where the side walls 100 c and 100 d meet wall 100 e can be rounded and have a radius of approximately 0.1″. The rear edge 100 b of thebody part 100 is a continuous straight edge that is configured to make contact with shoulder 80 c of back cap 80 (seeFIG. 18 ). - FIGS. 8A-I show various views of the
left body part 110. Thebody part 110 can preferably be made as one-piece structure by e.g., injection molding. In this regard, it is preferably made of a plastic or synthetic resin such as, e.g., ABS plastic. Thebody part 110 may also have be made of ABS—Metallic Silver and have a finish designated as SPI-A2. Additionally, thebody part 110 may have an overall length that is approximately 3.04″ (i.e., between edges 110 a and 110 b). This will ensure that the assembled lancet device can have an overall length of approximately 4.1″. Of course, other materials and/or finishes may be utilized, without leaving the scope of the invention. Moreover, thebody part 110 may even be made of a plurality of sections of parts which are joined together to form thecomplete body part 110, without leaving the scope of the invention. - The
body part 110 preferably has a front curved edge 110 a and includes circular and/or curved side edges 110 a 1. The radius of curved edge 110 a may be approximately 0.38″. As will be described later on with regard toFIG. 16 , the front edge 110 a is configured to abut a curved edge 20 a offront cap 20 until contact occurs between circular and/or curved edge 20 a and edge 110 a. A recess 110 a 2 is disposed between front edge 110 a and connecting wall 110 a 3. This recess 110 a 2 is arranged on each ofsides 110 c, 110 d, and possibly on side 110 e. Moreover, they have a rounded bottom that is configured to receive or otherwise engage projections 20 c (seeFIG. 16C ). In this regard, the projections 20 c similarly has a rounded edge that generally corresponds to the rounded bottom of recesses 110 a 2. Of course, the recess 110 a 2 can be either a partial recess or a continuous one, i.e., it can extend continuously from side 110 c toside 110 d. Alternatively, it can instead be formed as intermitted recesses or it may have the form of a single short recess that is centrally arranged with respect to walls 110 c and 100 c andwalls 100 d and 110 d (when thebody parts body part 110 can have the projection while thefront cap 20 has the recess. Of course, other connecting mechanisms, whether conventional or otherwise, may also be utilized in place of the projection and recess connection. - The
body part 110 also preferably has a curved lower surface LS. An inwardly curved surface 110 l is also provided which may have a radius of approximately 1.76″. Thelower body part 110 additionally preferably includes two plate-like projections orwalls 110 h and 110 i which are generally arranged to connectsides 110 c and 110 d. The purpose of theseprojections 110 h and 110 i is to axially retain thecam wheel 60 in the same way described above with regard towalls projections 110 h and 110 i are spaced apart a distance similar toprojections FIG. 7 . Theseprojections 110 h and 110 i also similarly have inwardly curved recesses of different sizes which allow portions of thecam wheel 60 to axially project therethrough (see e.g.,FIG. 1 ). As can be seen inFIG. 1 ,walls walls 100 i and 110 i are generally aligned with one another and have inwardly curved recesses that serve as a bearing for surface 60 i. A C-shaped projection 110 j extends from wall 110 c of thebody part 110 in the same way as projection 100 j of body part 100 (but oppositely arranged therefrom). This projection 110 j forms the other half of a bearing system for thetrigger 50. Together with the projection 100 j (seeFIG. 7 ), i.e., right half of the bearing system, the parts 100 j and 110 j form two circular bearing supports for thetrigger 50. As will be described later on with regard toFIG. 17 , thejournal elements 50 c of thetrigger 50 are mounted to or within the bearing supports formed by parts 100 j/110 j. Thebody part 110 additionally includes connecting ribs 110 a 3 and 110 k that provides strength to thebody part 110 and act to axially guide the holdingmember 30/40. In order to allow the holdingmember 30 move freely within the lancet device LD and without being obstructed by the ribs 110 a 3 and 110 k, circular or curved recesses (seeFIGS. 8D, 8E and 8G) are formed in the center of the ribs 110 a 3 and 110 k. These recesses of the ribs 110 a 3 and 110 k can have a radius of approximately 0.17″. - The
body part 110 further preferably includes a polygonal or square shapedmain projection 110 m that is generally centrally disposed relative tosides 110 c and 110 d. The purpose of thisprojection 110 m is to axially and/or non-rotatably guide the holdingmember 30/40 within the lancet device and to serve as stop surfaces for springs S1 and S2 (see e.g.,FIG. 1 ). Theprojection 110 m has a polygonal (i.e., four sided or square) shaped outer surface. A left side surface of theprojection 110 m serves a contact or engage right end of spring S1 (see e.g.,FIG. 1 ). A right side surface of theprojection 110 m serves a contact or engage left end of spring S2 (see e.g.,FIG. 1 ). Theprojection 110 m also has an inner recess or blind opening. This opening is mainly for ease of manufacture and to reduce material costs. As can be seen fromFIG. 4 , the length of theprojection 110 m is sized toabut projection 100 m ofbody part 100 whenbody parts projections body parts projection slot 40 f of theback portion 40 of holdingmember 30/40. - The
body part 110 also preferably includes circular or curved indented side portions 110 q and 110 n. Recess 110 q may have a radius of approximately 0.82″. Recess 110 n may have a radius that is greater than approximately 1″. As described previously, recessed portion 110 n allows a user to access thecam wheel 60. That way, the user can use a finger to rotate thecam wheel 60 from side 110 e. As seen inFIG. 8I , thesides 110 c and 110 d can be angled with an angle “a” of approximately 7 degrees. Thesides 110 c and 110 d can also have outer surfaces US and LS which are curved outwardly in the length direction (i.e., seeFIG. 8A ) and have a radius of approximately 30″ and 55″ respectively. The corners 110 s where theside walls 110 c and 110 d meet wall 110 e can be rounded and have a radius of approximately 0.1″. The rear edge 110 b of thebody part 110 is preferably a continuous straight edge that is configured to make contact with shoulder 80 c of back cap 80 (seeFIG. 18 ). - As discussed above, surface 110 c extends from front edge 110 a to rear edge 110 b, and may have a radius of approximately 30″. Alternatively, it may be essentially straight. Arranged within the curved side 110 c is a tear-drop shaped through opening 110 f (note that the full opening is defined by
partial opening 100 f and partial opening 110 f when the two body parts are connected). This opening 110 f is sized and configured to receive thepush button portion 50 a of the trigger 50 (seeFIG. 17 ). Of course, the opening 110 f can have any desired size, shape or configuration provided it allows a user access to thetrigger 50 and provided that it generally corresponds to the size, shape and configuration of thetrigger 50. The opening 110 f is formed in the upper wall 110 c near an inwardly projecting shoulder 110 g. As was described previously, this shoulder 110 g (as withshoulder 100 g) is sized, shaped and/or configured to be engaged by the deflectingmember 30 c (seeFIG. 9 ). In this regard, the projection 110 g has a straight contact surface that is generally parallel to edge 110 b and a bottom surface or edge that can range from being generally perpendicular to edge 110 b to being tapered or angled by as much as 15 degrees or more. As will be described later on with regard toFIG. 9 , the straight contact surface of projection shoulder 110 g is configured to be engaged bysurface 30 c 1 of deflectingmember 30 c. - FIGS. 9A-D show various views of the
front portion 30 of the two-piece holding member 30/40. Thefront portion 30 can preferably be made as one-piece structure by e.g., injection molding. In this regard, it is preferably made of a plastic or synthetic resin such as, e.g., Delrin plastic. Thefront portion 30 may also be made of Delrin—Natural and have a finish designated as SPI-C1. Additionally, thefront portion 30 may have an overall length that is approximately 1.6″ (i.e., betweenedges 30 a and 30 b). Of course, other materials and/or finishes may be utilized, without leaving the scope of the invention. Moreover, thefront portion 30 may even be made of a plurality of sections of parts which are joined together to form thecomplete front portion 30, without leaving the scope of the invention. -
Front portion 30 preferably has afront end 30 a and a cylindrical section 30 d which may have a diameter of approximately 0.32″. Afront opening 30 e is arranged within the cylindrical section 30 d. Theopening 30 e extends from a wall 30 g to edge 30 a. The diameter “d” of theopening 30 e at theedge 30 a may be approximately 0.26″ and may taper slightly inwards, e.g., by approximately 0.25 degrees (per side), i.e., towards wall 30 g. Thistapered opening 30 e is sized and configured to securely and/or snugly retain and receive the lancet 10 (see e.g.,FIG. 1 ) which may be a conventional lancet. Axial slot 30 h and circumferential slot 30 m allow walls of theopening 30 e to expand and contract with removal and replacement of thelancet 10. Thefront portion 30 of holdingmember 30/40 also includes another cylindrical section 30 i which may have a diameter of approximately 0.46″. Anotherinternal opening 30 f extends from shoulder 30 l to a wall 30 g. Theopening 30 f is sized and configured to receive spring S1 (see e.g.,FIG. 1 ). The internal diameter of theopening 30 f at the shoulder 30 l may be approximately 0.24″ and may taper slightly, e.g., by approximately 0.25 degrees (per side), towards wall 30 g. Cylindrical section 30 i also has an internal opening 30 j that extends from edge 30 b to shoulder 30 l. The opening 30 j is sized and configured to receive end 40 a ofrear portion 40 of holdingmember 30/40 (see e.g.,FIG. 1 ). - A deflecting
member 30 c preferably extends from cylindrical section 30 i. This deflectingmember 30 c has astop surface 30 c 1 which is configured to abut shoulders 100 a 3 and 110 a 3 of thebody parts upper surface 30c 2 of the deflectingmember 30 c, nearend 30 c 1, is designed to be engaged by the trigger 50 (seeFIG. 1 ). Specifically, thissurface 30c 2 is configured to be engaged byprojection 50 e of thetrigger 50. As explained above, the deflectingmember 30 c is capable of deflecting inwards towards thefront portion 30 when it is forced inwards towards holdingmember 30/40. However, because the deflectingmember 30 c acts like a natural spring, the deflectingmember 30 c is capable of deflecting away from thefront portion 30 when it is not being forced towards holdingmember 30/40. In this regard, the deflectingmember 30 c is formed with an angle “a” of approximately 2 degrees relative to cylindrical surface 30 i. Theend 30 c 1 of the deflectingmember 30 c can be spaced from surface 30 d by approximately 0.09″. In thearea 30c 2 where the deflectingmember 30 c is engaged by theprojection 50 e of thetrigger 50, the outer surface may be parallel to cylindrical surface 30 d. Thus, the distance “sp” can be about 0.09″. The deflectingmember 30 c also has a width “w” (measured in the direction ofFIG. 9D ) of approximately 0.1″. - Inner diameter 30 j of
front portion 30 also preferably includes a continuous rounded recess 30 k which is sized and shaped to receive the continuous rounded projection 40 c of therear portion 40. In this way, the twoparts part 30 and the recess formed onpart 40 without leaving the scope of the invention. Moreover, the recess and projection need not be made continuous and can instead be intermittently formed. The invention also contemplates other connecting mechanisms besides a projection/recess connection such as, e.g., an adhesive attachment. - FIGS. 10A-C show the
rear portion 40 of the two-piece holding member 30/40. The length between end 40 a and end 40 b can be approximately 1.72″. As discussed above, front end ofrear portion 40 has a projection 40 c which engages recess 30 k of thefront portion 30. A cylindrical section 40 d extends from projection 40 c to circumferential shoulder 40 e. The cylindrical section 40 d may have a diameter of approximately 0.32″. Between the projection 40 c and end 40 a, the outer surface may taper or curve inwards to facilitate entry of end 40 a into opening 30 j. A through opening 40 l is arranged within the cylindrical section 40 d. The opening 40 l extends from end 40 a to end 40 b. The diameter of the opening 40 l may be approximately 0.24″ and, at the edge 40 b, may be approximately 0.244″ and may taper slightly, e.g., by approximately 0.25 degrees (per side), towards end 40 a. This tapered opening section 40 g is sized and configured to securely retain and receive the plug 90 (see e.g.,FIG. 1 ). The opening 40 l is sized and configured to receive springs S1 and S2 (see e.g.,FIG. 1 ). A recess 40 h is arranged within opening 40 g and is designed to receive projection 90 d of plug 90 (seeFIG. 12 ). The rounded recess 40 h may be continuous and may be sized and shaped to receive the continuous rounded projection 90 d of theplug 90. In this way, theparts part 40 and the recess formed onpart 90 without leaving the scope of the invention. Moreover, the recess and projection need not be made continuous and can instead be intermittently formed. The invention also contemplates other connecting mechanisms besides a projection/recess connection such as, e.g., an adhesive attachment. - End 40 b of the
rear part 40 also preferably includes three projections 40 l, 40 j and 40 k. Short projections 40 j and 40 k extend in the direction of the axis of therear portion 40 and are arranged opposite one another, i.e., 180 degrees apart. These projections 40 j and 40 k may have a length of approximately 0.21″ and a width of approximately 0.05″. Short projections 40 j and 40 k also have stop surfaces 40 j 1 and 40 k 1. These surfaces 40 j 1 and 40 k 1 are adapted to be engaged and/or contacted by surface 70 d of theinner sleeve 70 when theback cap 80 is moved backwards to load the lancet device (seeFIG. 5 ).Longer projection 40 i includes a stop shoulder orsurface 40 i 1. As explained previously, thestop surface 40 i 1 engages and/or contacts the various cam surfaces 60 e 1-60e 8 of thecam wheel 60. Thus, thestop surface 40 i 1 serves to adjust the depth of the lancet needle based upon the position of thecam wheel 60, as will be described later on. As will be explained more clearly later on, theprojection 40 i is configured to slide within arecess 70 e of theinner sleeve 70 when theback cap 80 is moved from the positions shown inFIGS. 1 and 5 . An elongated throughslot 40 f is arranged on the cylindrical section 40 d. As discussed above, thisslot 40 f is sized and configured to receiveprojections body parts slot 40 f can be approximately 0.16″ while the length SL of theslot 40 f can be approximately 0.74″. Theslot 40 f also has rounded ends whose radius SR can be approximately 0.08″. The diameter of shoulder 40 e may be approximately 0.42″. - As discussed above, continuous recess or indentation 40 h is sized and configured to receive a projection 90 d of the
end plug 90. In this regard, the recess 40 h may have a radius of approximately 0.007″ and a depth of approximately 0.004″. As can be seen inFIG. 1 , diameter 90 c of theend plug 90 is configured to slide into opening 40 g of end 40 b. Once the projection 90 d engages recess 40 h, theend plug 90 is secured to therear portion 40 of holdingmember 30/40. As explained previously, surface 90 b of theend plug 90 serves to engage or contact one end of spring S2. The end plug 90 is installed once springs S1 and S2 are arranged within theopenings 30 f and 40 l. - FIGS. 11A-E show various views of the
cam wheel 60. Thecam wheel 60 can preferably be made as one-piece structure by e.g., injection molding. In this regard, it is preferably made of a plastic or synthetic resin such as, e.g., ABS plastic. Thecam wheel 60 may also have be made of ABS—Dark Blue and have a finish designated as MT-11040. Additionally, thecam wheel 60 may have an overall diameter that is approximately 0.71″. Of course, other materials and/or finishes may be utilized, without leaving the scope of the invention. Moreover, thecam wheel 60 may even be made of a plurality of sections of parts which are joined together to form thecomplete cam wheel 60, without leaving the scope of the invention. - The
cam wheel 60 preferably has an outer circumferential surface 60 e that includes indicia I which may be numbers, e.g., numbers 1-8, or letters. Of course, any desired indicia may be utilized. This indicia I can be, e.g., pad printed or silk screen raised numbers in white ink. The height of the indicia I can be approximately 0.09″. A centrally disposedopening 60 j extends through thecam disk 60. Theopening 60 j may have a diameter of approximately 0.36″. As explained previously, theopening 60 j is sized and configured to rotate around and/or about surface 40 d. Surface 40 d also slides within opening 60 j when holdingmember 30/40 moves within lancet device LD. Thecam wheel 60 also includes an enlarged diameter opening 60 k that is defined by annular cam surfaces 60 e 1-60e 8 and annular shoulder 60 a. The diameter of the cylindrical surface 60 c is sized to rotate (with a clearance) within the circular bearing recess formed by projectingwalls cam wheel 60 includes a plurality of cam surfaces 60 e 1-60e 8 formed on a cam section 60 e. As can be partially seen inFIG. 11B , the cam surfaces 60 e 1-60e 8 are all spaced from edge 60 a by different amounts. As was explained previously, these surfaces 60 e 1-8 are configured to be contacted bystop surface 40 i 1 of the holdingmember 30/40. Thus, for example, when contact is made betweenstop surface 40 i 1 and surface 60 e 1, the lancet needle will penetrate to its deepest setting. On the other hand, when contact is made betweenstop surface 40 i 1 and surface 60e 8, the lancet needle will penetrate to its shallowest setting. Of course, surfaces 60 e 2-60e 7 will set the penetrating depth in between these extreme settings. Although, thecam wheel 60 is configured with eight settings (designated by the number of cam surfaces and the indicia), thecam wheel 60 can have any number of desired settings that can range from two to as many as 20 or more, if desired. The distance or width “w1” can be approximately 0.16″ whereas the width “w2” can be approximately 0.33″. - A cylindrical recess 60 i is formed between end 60 b and annular surface 60 f. The recess surface 60 i is sized to rotate (with a clearance) within the circular bearing recess formed by projecting
walls 100 i and 110 i. Thecam wheel 60 also includes a plurality of angled and/o undulating surfaces 60 b 1 which form pointed tips 60b 2. As was explained previously, these surfaces 60 b 1 engage with projection orpawl 100 p and served to temporarily retain thecam wheel 60 in a desired set-depth position. A plurality of raised textured portions 60 h are arranged between the indicia I. These allow the user to more easily grip thecam wheel 60 so as to cause its rotation. As was described with regard toFIG. 8 , thecam wheel 60 partially projects throughslot 110 p. - With reference to
FIG. 11E , it can be seen that indicia numbers 1-8 can be arranged to correspond to the annular cam surfaces 60 e 1-60e 8 based upon the position ofprojection 40 i. AlthoughFIG. 11E shows one possible arrangement, it should be noted that the cam surfaces 60 e 1-60e 8 can be arranged in any desired arrangement relative to the indicia and stopprojection 40 i, provided that the correct cam surface corresponds to the desired indicia setting. - FIGS. 12A-C show various views of the
end plug 90. The end plug 90 can preferably be made as one-piece structure by e.g., injection molding. In this regard, it is preferably made of a plastic or synthetic resin such as, e.g., Delrin plastic. The end plug 90 may also be made of Delrin—Natural and have a finish designated as SPI-C1. Additionally, theend plug 90 may have an overall length L that is approximately 0.31″ (i.e., between edges 90 e and 90 b). Of course, other materials and/or finishes may be utilized, without leaving the scope of the invention. Moreover, theend plug 90 may even be made of a plurality of sections of parts which are joined together to form thecomplete end plug 90, without leaving the scope of the invention. - The end plug 90 preferably has a rear planar wall 90 e and a front planar wall 90 b. A
shoulder 90 f is arranged between surfaces 90 e and 90 b. The diameter of cylindrical surface 90 a can be approximately 0.42″. The diameter of cylindrical surface 90 c can be sized to slide into opening 40 g. A projection 90 d extends from surface 90 c and is configured to engage recess 40 h. The projection 90 d may have a radius of 0.007″ and may extend fromsurface 90 f by approximately 0.004″. End 90 b can also have a chamfer that extends from surface 90 c. - FIGS. 13A-B show various views of the plunger spring S1. The spring S1 is preferably be made as one-piece structure. In this regard, it is preferably made of 0.05 mm wire. The spring S1 may also have be made of stainless steel 0.05 mm wire. Additionally, the spring S1 may have an overall freelength of approximately 36.7 mm and an outer diameter of approximately 6.2 mm. In this way, the spring S1 will be able to move freely within
openings 30 f and 40 l. Of course, other materials may be utilized, without leaving the scope of the invention. - FIGS. 14A-B show various views of the return spring S2. The spring S2 is preferably be made as one-piece structure. In this regard, it is preferably made of 0.05 mm wire. The spring S2 may also have be made of stainless steel 0.05 mm wire. Additionally, the spring S2 may have an overall freelength of approximately 25.5 mm and an outer diameter of approximately 6.2 mm. In this way, the spring S2 will be able to move freely within opening 40 l. Of course, other materials may be utilized, without leaving the scope of the invention.
- FIGS. 15A-B show various views of the cocking spring S3. The spring S3 is preferably be made as one-piece structure. In this regard, it is preferably made of 0.025 mm wire. The spring S3 may also have be made of stainless steel 0.025 mm wire. Additionally, the spring S3 may have an overall freelength of approximately 13.6 mm and an outer diameter of approximately 10.1 mm. In this way, the spring S3 will be able to move freely over surface 40 d and
projections 40 i, 40 j and 40 k. Of course, other materials may be utilized, without leaving the scope of the invention. - FIGS. 16A-E show various views of the
front cover 20. Thefront cover 20 can preferably be made as one-piece structure by e.g., injection molding. In this regard, it is preferably made of a plastic or synthetic resin such as, e.g., ABS plastic. Thefront cover 20 may also be made of ABS—Light Blue and have a finish designated as SPI-A2. Additionally, thefront cover 20 may have an overall length that is approximately 3/4″ (i.e., between left end of projection 20 c and end 20 f). Of course, other materials and/or finishes may be utilized, without leaving the scope of the invention. Moreover, thefront cover 20 may even be made of a plurality of sections of parts which are joined together to form the completefront cover 20, without leaving the scope of the invention. - The
front cover 20 preferably has a front wall 20 f that includes a circular and/or curved indentation 20 d (i.e., defining plane P) and a centrally disposed through opening 20 e (i.e., defining lancet opening LO). The radius of this indentation 20 d may be approximately 3/8″ and the diameter of the through opening 20 e may be approximately 0.13″. Of course, the invention also contemplates a plane P which is straight or which curves outwardly (not shown). As was described previously, the left edges 20 c are configured to slide into front edges 100 a and 110 a until contact occurs between circular and/or curved edges 20 b and edges 100 a 1 and 110 a 1. The projections 20 c may have a radius of approximately 0.02″. As explained previously, these projections 20 c are configured to engage with the recesses 100 a 2 and 110 a 2 (seeFIGS. 7A and 8C ). - Side walls 20 g and 20 h are preferably tapered inwardly from edge 20 a to surface 20 d and may form rounded corners (e.g., with a radius of approximately 0.1″) where walls 20 g and 20 h meets wall 20 d. Walls 20 g and 20 h can also be curved along their length (see
FIG. 16C ), having a radius of approximately 30″, and may also be curved outwardly (i.e., convex, seeFIG. 16C ). Side walls 20 g and 20 h may further be formed of tapered surfaces which meet at a center (seeFIG. 16E ). These surfaces may tapered outwards from a center at an angle “a” of approximately 7 degrees. Rounded corners 20 m (e.g., with a radius of approximately 0.1″) are provided between walls 20 g-j. The width “w1” of thefront cap 20 can be approximately 1/2″ while the height H1 can be approximately 0.56″ (seeFIG. 16E ). Walls 20 g and 20 h can also include raised and/or textured surfaces 20 k which allow a user to more easily grip thefront cap 20, thus facilitating its removal. Similarly, walls 20 i and 20 j can also include raised and/ortextured surfaces 201 which allow a user to more easily grip thefront cap 20. The width “w2” of thefront cap 20 can be approximately 0.38″ and can taper inwards by about 1 degree per side towards end 20 d. - FIGS. 17A-G show various views of the
trigger 50. Thetrigger 50 can preferably be made as one-piece structure by e.g., injection molding. In this regard, it is preferably made of a plastic or synthetic resin such as, e.g., ABS plastic. Thetrigger 40 may also be made of ABS—Red and have a finish designated as SPI-A2. Additionally, thetrigger 50 may have an overall length that is approximately 1.1″. Of course, other materials and/or finishes may be utilized, without leaving the scope of the invention. Moreover, thetrigger 50 may even be made of a plurality of sections of parts which are joined together to form thecomplete trigger 50, without leaving the scope of the invention. - The
trigger 50 preferably has a rear end that includes a rounded projection 50 d. This rounded projection 50 d is configured to contact an inner surface ofbody parts 100 and 110 (seeFIG. 1 ), and serves to brace or counter the movement of thetrigger 50 when thetrigger 50 is pressed into the lancet device (SeeFIG. 2 ). The projection 50 d may have a radius of approximately 0.03″. Thetrigger 50 also has front end 50 b that includes a roundedprojection 50 e. Thisrounded projection 50 e is configured to contactsurface 30c 2 of deflectingmember 30 c of the holdingmember 30/40 (seeFIG. 9 ) upon movement of thetrigger 50, when thetrigger 50 is pressed into the lancet device. Theprojection 50 e may have a radius of approximately 0.03″. Thetrigger 50 also includes a connecting member 50 g which connects thepush button 50 a to the support 50 f. Two shaft members orjournals 50 c project from opposite sides of the support 50 f. Thejournals 50 c may have a diameter of approximately 0.06″ and the width “w1” may be 0.36″. Thesejournals 50 c also have rounded ends whose radius can be approximately 0.03″. As explained previously, thesejournals 50 c are configured to be mounted in the bearing supports formed by projections 100 j and 110 j. In this regard, the openings formed by these projections 100 j and 110 j should be sized to be the same or slightly larger than the diameter ofjournals 50 c. In this way, thejournals 50 c can fit snugly in the supports 100 j/110 j. The width (measured in the direction ofFIG. 17E ) of the support 50 f may be approximately 0.1″. - The
push button 50 a preferably has a tear-drop shape and includes a inwardly curved (i.e., concave) surface that has a radius of approximately 1.9″. A lip member 50 b projects from the front of thepush button 50 a. This lip member 50 b is approximately 0.06″ wide and may extend from thepush button 50 a by approximately 0.04″. The thickness T2 of the lip member 50 b (measured in the direction ofFIG. 17F ) can be approximately 0.02″ and the distance T1 can be approximately 0.04″. Angle “x” can be approximately 5 degrees and angle “y” can be approximately 18 degrees. The lip member 50 b limits the upward movement of thepush button 50 a by contacting an inner surface of thebody parts trigger 50 is in the original non-deflected position (see e.g.,FIG. 1 ). Thepush button 50 a can have a width “w2” of approximately 0.25″. The length L1 can be approximately 0.51″ while the length L2 can be approximately 0.57″. Finally, thecurved surface 50 a can also include a texture (seeFIG. 17G ) formed of projections and recesses to prevent a user's finger from slipping off of thebutton 50 a. - As explained above with regard to
FIG. 1 , thetrigger 50 is designed to preferably deflect inwardly when a user pushes against thepush button 50 a (seeFIG. 2 ) and to return to an original position (seeFIG. 1 or 3). In this regard, the deflection occurs in the area betweenjournals 50 c and connecting element 50 g and/or possibly somewhat between projection 50 d andjournals 50 c. The design is such that the material properties of thetrigger 50 allows it to act like a natural spring. - FIGS. 18A-E show various views of the
back cap 80. Theback cap 80 can preferably be made as one-piece structure by e.g., injection molding. In this regard, it is preferably made of a plastic or synthetic resin such as, e.g., ABS plastic. Theback cap 80 may also be made of ABS—Light Blue and have a finish designated as SPI-A2. Additionally, theback cap 80 may have an overall length L2 that is approximately 0.9″ (i.e., between ends 80 a and 80 b). Of course, other materials and/or finishes may be utilized, without leaving the scope of the invention. Moreover, theback cap 80 may even be made of a plurality of sections of parts which are joined together to form thecomplete back cap 80, without leaving the scope of the invention. - The
back cap 80 preferably has a rear wall 80 b that has a planar outer surface and a planar inner surface 80 d. Theback cap 80 also has an opening 80 e that extends from end 80 a to surface 80 d. This opening 80 e is generally rectangular and has a width “w1” of approximately 0.49″ and a width “w2” of approximately 0.66″. This opening 80 e extends from edge 80 a and tapers inwardly towards surface 80 d at an angle of approximately 1 degrees (per side). The width “w3” betweenouter surfaces outer surfaces 80 f and 80 g may be approximately 0.72″ and may taper outwardly from edge 80 a to shoulder 80 c by approximately 1 degree per side. The length L1 from end 80 b to shoulder 80 c may be approximately 0.49″. Thewalls 80 f-80 i are configured to slide into rear ends 100 b and 110 b until contact occurs between the shoulder 80 c and edges 100 b and 110 b. As will be explained later on with regard toFIG. 19 , theback cap 80 and specifically opening 80 e, is configured to receive or otherwise engage with theinner sleeve 70. Although not shown, a recess and projection connection may be utilized between thesleeve 70 and backcap 80. Of course, other connecting mechanisms, whether conventional or otherwise, may also be utilized in place of the projection and recess connection such as, e.g., a friction fit connection and/or adhesive attachment. -
Side walls walls 80 j-80 m may also have a radius of approximately 1.44″ and may be outwardly curved, i.e., concave.Walls 80 l and 80 m may also have texturedsurfaces 80 n and thewalls FIG. 18B ,walls 80 l and 80 m may be formed by tapered surfaces that meet at the center and which have an angle “a” of approximately of 7 degrees. - FIGS. 19A-C show various views of the
inner sleeve 70. Theinner sleeve 70 can preferably be made as one-piece structure by e.g., injection molding. In this regard, it is preferably made of a plastic or synthetic resin such as, e.g., ABS plastic. Theinner sleeve 70 may also be made of ABS—Light Blue and have a finish designated as SPI-C1. Additionally, theinner sleeve 70 may have an overall length L that is approximately 0.6″ (i.e., betweenedges 70 a and 70 b). Of course, other materials and/or finishes may be utilized, without leaving the scope of the invention. Moreover, theinner sleeve 70 may even be made of a plurality of sections of parts which are joined together to form the completeinner sleeve 70, without leaving the scope of the invention. - The
inner sleeve 70 has a front wall 70 a that has a planar outer surface and a planar inner surface 70 d. Anopening 70 c is provided in the wall 70 a. Thisopening 70 c has a circular central part and a generallypolygonal recess 70 e.Recess 70 e is approximately 0.05″ wide. As was previously explained, therecess 70 e is sized and configured to receiveprojection 40 i. Theinner sleeve 70 is able slide over the rear portion 40 (from the front) of the holdingmember 30/40 when the lancet device is assembled. - Surfaces 70 f-70 i are preferably tapered to match the tapered inner surfaces of opening 80 e. In this way, when the
sleeve 70 is inserted intoback cap 80, the shoulder 70 j will abut edge 80 a of theback cap 80. The width “w1” can be approximately 0.42″. The width “w2” can be approximately 0.53″. The width “w3” can be approximately 0.65″. Finally, the width “w4” can be approximately 0.72″. Thewalls 70 h and 70 i can taper from walls 70 f and 70 g by an angle “a” of approximately 7 degrees from a center position (seeFIG. 19B ). - All the parts of the lancet device, with the exception of the springs S1-S3 (which can be made of spring steel) and with the exception of the lancet needle (which can be a conventional metal needle mounted to a conventional plastic lancet 10), may be made from plastic materials and can be formed using conventional injection molding techniques or other known manufacturing methods. The cam disk for example can be integrally formed with peripheral grooves and/or projections (similar to a coin), and with the indicating marks. However, when practical, other materials and manufacturing processes may also be utilized.
- It is noted that the foregoing examples have been provided merely for the purpose of explanation and are in no way to be construed as limiting of the present invention. While the present invention has been described with reference to an exemplary embodiment, it is understood that the words which have been used herein are words of description and illustration, rather than words of limitation. Changes may be made, within the purview of the appended claims, as presently stated and as amended, without departing from the scope and spirit of the present invention in its aspects. Although the present invention has been described herein with reference to particular means, materials and embodiments, the present invention is not intended to be limited to the particulars disclosed herein; rather, the present invention extends to all functionally equivalent structures, methods and uses, such as are within the scope of the appended claims.
Claims (44)
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/641,101 US7105006B2 (en) | 2003-08-15 | 2003-08-15 | Adjustable lancet device and method |
AU2004266638A AU2004266638A1 (en) | 2003-08-15 | 2004-08-13 | Adjustable lancet device and method |
CNB2004800303691A CN100450451C (en) | 2003-08-15 | 2004-08-13 | Adjustable lancet device and method |
CA002535785A CA2535785A1 (en) | 2003-08-15 | 2004-08-13 | Adjustable lancet device and method |
EP04780835A EP1663022A4 (en) | 2003-08-15 | 2004-08-13 | Adjustable lancet device and method |
PCT/US2004/026060 WO2005018421A2 (en) | 2003-08-15 | 2004-08-13 | Adjustable lancet device and method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/641,101 US7105006B2 (en) | 2003-08-15 | 2003-08-15 | Adjustable lancet device and method |
Publications (3)
Publication Number | Publication Date |
---|---|
US20050038464A1 US20050038464A1 (en) | 2005-02-17 |
US20050267505A9 true US20050267505A9 (en) | 2005-12-01 |
US7105006B2 US7105006B2 (en) | 2006-09-12 |
Family
ID=34136255
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/641,101 Expired - Lifetime US7105006B2 (en) | 2003-08-15 | 2003-08-15 | Adjustable lancet device and method |
Country Status (6)
Country | Link |
---|---|
US (1) | US7105006B2 (en) |
EP (1) | EP1663022A4 (en) |
CN (1) | CN100450451C (en) |
AU (1) | AU2004266638A1 (en) |
CA (1) | CA2535785A1 (en) |
WO (1) | WO2005018421A2 (en) |
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20080015503A1 (en) * | 2006-07-14 | 2008-01-17 | Roche Diagnostics Operations, Inc. | Injection device |
US20080077167A1 (en) * | 2006-06-15 | 2008-03-27 | Abbott Diabetes Care Inc. | Lancing Devices Having Depth Adjustment Assembly |
US20080195132A1 (en) * | 2007-02-08 | 2008-08-14 | Stat Medical Devices, Inc. | Push-button lance device and method |
WO2008121680A2 (en) * | 2007-03-30 | 2008-10-09 | Stat Medical Devices, Inc. | Lancet device with combined trigger and cocking mechanism and method |
US20100042131A1 (en) * | 2008-08-14 | 2010-02-18 | Abbott Diabetes Care Inc. | Cocking mechanism for lancing device |
US8834503B2 (en) | 1998-06-11 | 2014-09-16 | Stat Medical Devices, Inc. | Lancet having adjustable penetration depth |
US8864783B2 (en) | 2005-08-04 | 2014-10-21 | Bayer Healthcare Llc | Lancing device |
US8876846B2 (en) | 2005-11-03 | 2014-11-04 | Stat Medical Devices, Inc. | Disposable/single-use blade lancet device and method |
US8888804B2 (en) | 2003-08-15 | 2014-11-18 | Stat Medical Devices, Inc. | Adjustable lancet device and method |
US20160106349A1 (en) * | 2012-04-04 | 2016-04-21 | Dexcom, Inc. | Transcutaneous analyte sensors, applicators therefor, and associated methods |
Families Citing this family (81)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6036924A (en) | 1997-12-04 | 2000-03-14 | Hewlett-Packard Company | Cassette of lancet cartridges for sampling blood |
US6391005B1 (en) | 1998-03-30 | 2002-05-21 | Agilent Technologies, Inc. | Apparatus and method for penetration with shaft having a sensor for sensing penetration depth |
US8814896B2 (en) | 1999-11-02 | 2014-08-26 | Stat Medical Devices, Inc. | Single use lancet assembly |
US20050070945A1 (en) | 1999-11-02 | 2005-03-31 | Steven Schraga | Single use lancet assembly |
US8641644B2 (en) | 2000-11-21 | 2014-02-04 | Sanofi-Aventis Deutschland Gmbh | Blood testing apparatus having a rotatable cartridge with multiple lancing elements and testing means |
CA2448905C (en) | 2001-06-12 | 2010-09-07 | Pelikan Technologies, Inc. | Blood sampling apparatus and method |
US7025774B2 (en) | 2001-06-12 | 2006-04-11 | Pelikan Technologies, Inc. | Tissue penetration device |
CA2448902C (en) | 2001-06-12 | 2010-09-07 | Pelikan Technologies, Inc. | Self optimizing lancing device with adaptation means to temporal variations in cutaneous properties |
US7981056B2 (en) | 2002-04-19 | 2011-07-19 | Pelikan Technologies, Inc. | Methods and apparatus for lancet actuation |
US8337419B2 (en) | 2002-04-19 | 2012-12-25 | Sanofi-Aventis Deutschland Gmbh | Tissue penetration device |
US9427532B2 (en) | 2001-06-12 | 2016-08-30 | Sanofi-Aventis Deutschland Gmbh | Tissue penetration device |
AU2002344825A1 (en) | 2001-06-12 | 2002-12-23 | Pelikan Technologies, Inc. | Method and apparatus for improving success rate of blood yield from a fingerstick |
US9226699B2 (en) | 2002-04-19 | 2016-01-05 | Sanofi-Aventis Deutschland Gmbh | Body fluid sampling module with a continuous compression tissue interface surface |
US9795747B2 (en) | 2010-06-02 | 2017-10-24 | Sanofi-Aventis Deutschland Gmbh | Methods and apparatus for lancet actuation |
ES2352998T3 (en) | 2001-06-12 | 2011-02-24 | Pelikan Technologies Inc. | LANCETA ELECTRIC ACTUATOR. |
WO2002100254A2 (en) | 2001-06-12 | 2002-12-19 | Pelikan Technologies, Inc. | Method and apparatus for lancet launching device integrated onto a blood-sampling cartridge |
US8048097B2 (en) | 2001-08-14 | 2011-11-01 | Steven Schraga | Single use lancet assembly |
US7291117B2 (en) | 2002-04-19 | 2007-11-06 | Pelikan Technologies, Inc. | Method and apparatus for penetrating tissue |
US7175642B2 (en) | 2002-04-19 | 2007-02-13 | Pelikan Technologies, Inc. | Methods and apparatus for lancet actuation |
US9314194B2 (en) | 2002-04-19 | 2016-04-19 | Sanofi-Aventis Deutschland Gmbh | Tissue penetration device |
US7229458B2 (en) | 2002-04-19 | 2007-06-12 | Pelikan Technologies, Inc. | Method and apparatus for penetrating tissue |
US7717863B2 (en) | 2002-04-19 | 2010-05-18 | Pelikan Technologies, Inc. | Method and apparatus for penetrating tissue |
US9795334B2 (en) | 2002-04-19 | 2017-10-24 | Sanofi-Aventis Deutschland Gmbh | Method and apparatus for penetrating tissue |
US7232451B2 (en) | 2002-04-19 | 2007-06-19 | Pelikan Technologies, Inc. | Method and apparatus for penetrating tissue |
US7297122B2 (en) | 2002-04-19 | 2007-11-20 | Pelikan Technologies, Inc. | Method and apparatus for penetrating tissue |
US7901362B2 (en) | 2002-04-19 | 2011-03-08 | Pelikan Technologies, Inc. | Method and apparatus for penetrating tissue |
US7648468B2 (en) | 2002-04-19 | 2010-01-19 | Pelikon Technologies, Inc. | Method and apparatus for penetrating tissue |
US9248267B2 (en) | 2002-04-19 | 2016-02-02 | Sanofi-Aventis Deustchland Gmbh | Tissue penetration device |
US8579831B2 (en) | 2002-04-19 | 2013-11-12 | Sanofi-Aventis Deutschland Gmbh | Method and apparatus for penetrating tissue |
US7909778B2 (en) * | 2002-04-19 | 2011-03-22 | Pelikan Technologies, Inc. | Method and apparatus for penetrating tissue |
US7141058B2 (en) * | 2002-04-19 | 2006-11-28 | Pelikan Technologies, Inc. | Method and apparatus for a body fluid sampling device using illumination |
US7674232B2 (en) * | 2002-04-19 | 2010-03-09 | Pelikan Technologies, Inc. | Method and apparatus for penetrating tissue |
US7892183B2 (en) | 2002-04-19 | 2011-02-22 | Pelikan Technologies, Inc. | Method and apparatus for body fluid sampling and analyte sensing |
US8221334B2 (en) | 2002-04-19 | 2012-07-17 | Sanofi-Aventis Deutschland Gmbh | Method and apparatus for penetrating tissue |
US8702624B2 (en) | 2006-09-29 | 2014-04-22 | Sanofi-Aventis Deutschland Gmbh | Analyte measurement device with a single shot actuator |
US8784335B2 (en) | 2002-04-19 | 2014-07-22 | Sanofi-Aventis Deutschland Gmbh | Body fluid sampling device with a capacitive sensor |
US8267870B2 (en) | 2002-04-19 | 2012-09-18 | Sanofi-Aventis Deutschland Gmbh | Method and apparatus for body fluid sampling with hybrid actuation |
US7547287B2 (en) | 2002-04-19 | 2009-06-16 | Pelikan Technologies, Inc. | Method and apparatus for penetrating tissue |
US7563232B2 (en) * | 2002-04-19 | 2009-07-21 | Pelikan Technologies, Inc. | Method and apparatus for penetrating tissue |
US7491178B2 (en) | 2002-04-19 | 2009-02-17 | Pelikan Technologies, Inc. | Method and apparatus for penetrating tissue |
US7976476B2 (en) * | 2002-04-19 | 2011-07-12 | Pelikan Technologies, Inc. | Device and method for variable speed lancet |
US7371247B2 (en) * | 2002-04-19 | 2008-05-13 | Pelikan Technologies, Inc | Method and apparatus for penetrating tissue |
US7331931B2 (en) | 2002-04-19 | 2008-02-19 | Pelikan Technologies, Inc. | Method and apparatus for penetrating tissue |
US7713214B2 (en) | 2002-04-19 | 2010-05-11 | Pelikan Technologies, Inc. | Method and apparatus for a multi-use body fluid sampling device with optical analyte sensing |
US8715309B2 (en) | 2002-04-29 | 2014-05-06 | Steven Schraga | Lancet device |
US20040039407A1 (en) * | 2002-04-29 | 2004-02-26 | Steven Schraga | Lancet device |
US8574895B2 (en) | 2002-12-30 | 2013-11-05 | Sanofi-Aventis Deutschland Gmbh | Method and apparatus using optical techniques to measure analyte levels |
AU2003300154A1 (en) * | 2002-12-31 | 2004-07-29 | Pelikan Technologies Inc. | Method and apparatus for loading penetrating members |
US7494498B2 (en) * | 2003-03-24 | 2009-02-24 | Facet Technologies, Llc | Lancing device with floating lancet |
US7850621B2 (en) | 2003-06-06 | 2010-12-14 | Pelikan Technologies, Inc. | Method and apparatus for body fluid sampling and analyte sensing |
WO2006001797A1 (en) | 2004-06-14 | 2006-01-05 | Pelikan Technologies, Inc. | Low pain penetrating |
WO2005033659A2 (en) | 2003-09-29 | 2005-04-14 | Pelikan Technologies, Inc. | Method and apparatus for an improved sample capture device |
WO2005037095A1 (en) | 2003-10-14 | 2005-04-28 | Pelikan Technologies, Inc. | Method and apparatus for a variable user interface |
US7822454B1 (en) | 2005-01-03 | 2010-10-26 | Pelikan Technologies, Inc. | Fluid sampling device with improved analyte detecting member configuration |
US8668656B2 (en) | 2003-12-31 | 2014-03-11 | Sanofi-Aventis Deutschland Gmbh | Method and apparatus for improving fluidic flow and sample capture |
EP1751546A2 (en) | 2004-05-20 | 2007-02-14 | Albatros Technologies GmbH & Co. KG | Printable hydrogel for biosensors |
WO2005120365A1 (en) | 2004-06-03 | 2005-12-22 | Pelikan Technologies, Inc. | Method and apparatus for a fluid sampling device |
US8652831B2 (en) | 2004-12-30 | 2014-02-18 | Sanofi-Aventis Deutschland Gmbh | Method and apparatus for analyte measurement test time |
ATE472972T1 (en) * | 2005-04-04 | 2010-07-15 | Facet Technologies Llc | NARROW PROFILE LANCET DEVICE |
US20060247670A1 (en) * | 2005-05-02 | 2006-11-02 | Levaughn Richard W | Lancing device with automatic lancet release |
US20060247671A1 (en) * | 2005-05-02 | 2006-11-02 | Levaughn Richard W | Compact, multi-use micro-sampling device |
ES2547008T3 (en) * | 2006-03-15 | 2015-09-30 | Bayer Healthcare Llc | Puncture device with reduced one-hand vibration |
EP2010055B1 (en) | 2006-04-25 | 2018-01-10 | Facet Technologies, LLC | Lancing device with independent drive core |
TWM314048U (en) * | 2006-11-06 | 2007-06-21 | Apex Biotechnology Corp | Safety syringe |
CN201098127Y (en) * | 2007-10-26 | 2008-08-13 | 黄秋月 | Safety blood taking needle |
US9386944B2 (en) | 2008-04-11 | 2016-07-12 | Sanofi-Aventis Deutschland Gmbh | Method and apparatus for analyte detecting device |
EP2375985B1 (en) | 2008-12-18 | 2013-06-19 | Facet Technologies, LLC | Lancing device |
US9375169B2 (en) | 2009-01-30 | 2016-06-28 | Sanofi-Aventis Deutschland Gmbh | Cam drive for managing disposable penetrating member actions with a single motor and motor and control system |
US8317812B2 (en) * | 2009-07-29 | 2012-11-27 | Wah Leong Lum | Lancet device with lance retraction |
WO2011050142A1 (en) * | 2009-10-22 | 2011-04-28 | Facet Technologies, Llc. | Lancing device with improved guidance assembly |
USD634426S1 (en) | 2010-04-08 | 2011-03-15 | Facet Technologies, Llc | Lancing device |
EP2555680B1 (en) | 2010-04-09 | 2014-02-26 | Facet Technologies, LLC | Lancing device with tethered depth-control mechanism |
US8965476B2 (en) | 2010-04-16 | 2015-02-24 | Sanofi-Aventis Deutschland Gmbh | Tissue penetration device |
EP2790581B1 (en) | 2011-12-15 | 2016-06-08 | Facet Technologies, LLC | Latch mechanism for preventing lancet oscillation in a lancing device |
US9572922B2 (en) | 2012-12-21 | 2017-02-21 | Larry Leonard | Inventive diabetic systems, tools, kits, and supplies for better diabetic living and mobility |
WO2013155149A1 (en) | 2012-04-11 | 2013-10-17 | Facet Technologies, Llc | Lancing device with moving pivot depth adjust |
US10456069B2 (en) | 2012-04-12 | 2019-10-29 | Facet Technologies, Llc | Lancing device with side activated charge and eject mechanisms |
US10105086B2 (en) | 2012-08-27 | 2018-10-23 | Facet Technologies, Llc | Twist-to-charge mechanism of lancing device |
WO2016027192A1 (en) | 2014-08-21 | 2016-02-25 | Koninklijke Philips N.V. | A tongue advancer implant or removal tool for a tongue manipulation system |
USD806246S1 (en) | 2016-02-25 | 2017-12-26 | Steven Schraga | Lancet cover |
US11896234B2 (en) | 2018-01-26 | 2024-02-13 | Fluidx Medical Technology, Llc | Apparatus and method of using in situ solidifying complex coacervates for vascular occlusion |
Citations (32)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2823677A (en) * | 1955-01-17 | 1958-02-18 | Becton Dickinson Co | Lancet |
US3760809A (en) * | 1971-10-22 | 1973-09-25 | Damon Corp | Surgical lancet having casing |
US4064871A (en) * | 1976-05-11 | 1977-12-27 | Becton, Dickinson And Company | Device for making precise incisions for bleeding time testing and the like |
US4157086A (en) * | 1975-10-13 | 1979-06-05 | Farmitalia Carlo Erba S.P.A. | Apparatus for providing skin cuts to a predetermined measure |
US4438770A (en) * | 1979-03-23 | 1984-03-27 | Hans Peter Olof Unger | Skin incising device |
US4539988A (en) * | 1983-07-05 | 1985-09-10 | Packaging Corporation International | Disposable automatic lancet |
US4553541A (en) * | 1981-03-23 | 1985-11-19 | Becton, Dickinson And Co. | Automatic retractable lancet assembly |
US4643189A (en) * | 1985-02-19 | 1987-02-17 | W. T. Associates | Apparatus for implementing a standardized skin incision |
US5133730A (en) * | 1991-05-15 | 1992-07-28 | International Technidyne Corporation | Disposable-retractable finger stick device |
US5196025A (en) * | 1990-05-21 | 1993-03-23 | Ryder International Corporation | Lancet actuator with retractable mechanism |
US5304193A (en) * | 1993-08-12 | 1994-04-19 | Sam Zhadanov | Blood lancing device |
US5314441A (en) * | 1992-10-16 | 1994-05-24 | International Technidyne Corporation | Disposable slicing lancet assembly |
US5527333A (en) * | 1994-09-09 | 1996-06-18 | Graphic Controls Corporation | Slicing disposable blood sampling device |
US5527334A (en) * | 1994-05-25 | 1996-06-18 | Ryder International Corporation | Disposable, retractable lancet |
US5529581A (en) * | 1994-05-17 | 1996-06-25 | International Technidyne Corporation | Lancet device for creating a skin incision |
US5545174A (en) * | 1994-01-11 | 1996-08-13 | Sherwood Medical Company | Finger stick device |
US5554166A (en) * | 1993-06-21 | 1996-09-10 | Boehringer Mannheim Gmbh | Blood lancet device for withdrawing blood for diagnostic purposes |
US5571132A (en) * | 1995-06-06 | 1996-11-05 | International Technidyne Corporation | Self activated finger lancet |
US5589156A (en) * | 1994-05-02 | 1996-12-31 | Henry; Richard A. | Prilocaine and hydrofluourocarbon aerosol preparations |
US5613978A (en) * | 1996-06-04 | 1997-03-25 | Palco Laboratories | Adjustable tip for lancet device |
US5662672A (en) * | 1996-05-23 | 1997-09-02 | Array Medical, Inc. | Single use, bi-directional linear motion lancet |
US5730753A (en) * | 1995-07-28 | 1998-03-24 | Apls Co., Ltd. | Assembly for adjusting pricking depth of lancet |
US5772677A (en) * | 1996-09-24 | 1998-06-30 | International Technidyne Corporation | Incision device capable of automatic assembly and a method of assembly |
US5797940A (en) * | 1997-05-30 | 1998-08-25 | International Technidyne Corporation | Adjustable skin incision device |
US5916230A (en) * | 1997-06-16 | 1999-06-29 | Bayer Corporation | Blood sampling device with adjustable end cap |
US6042595A (en) * | 1999-03-02 | 2000-03-28 | Apls Co., Ltd. | Lancet apparatus for producing a precisely controlled incision |
US6207184B1 (en) * | 1998-06-18 | 2001-03-27 | Ssp Co., Ltd. | Hydrophilic adhesive masses |
US6358265B1 (en) * | 2000-07-18 | 2002-03-19 | Specialized Health Products, Inc. | Single-step disposable safety lancet apparatus and methods |
US6395495B1 (en) * | 1983-09-15 | 2002-05-28 | Institut Pasteur | Methods and kits for detecting antibodies against an HIV variant |
US20030028126A1 (en) * | 2001-05-05 | 2003-02-06 | Hans List | Blood withdrawal system |
US6558402B1 (en) * | 1999-08-03 | 2003-05-06 | Becton, Dickinson And Company | Lancer |
US6635674B1 (en) * | 1998-11-06 | 2003-10-21 | Bristol-Myers Squibb Co. | Pharmaceutical preparations for external use containing non-steroidal anti-inflammatory and analgesic agents |
Family Cites Families (71)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US676678A (en) | 1901-04-24 | 1901-06-18 | George W Webb | Nut-lock. |
US1135465A (en) | 1914-07-01 | 1915-04-13 | William M Pollock | Lancet. |
US2848809A (en) | 1956-02-24 | 1958-08-26 | John S Crowder | Retractable scratch awl |
US3589213A (en) | 1968-08-16 | 1971-06-29 | Mccrosky Tool Corp | Turret tool post and handle assembly |
DE2657053C3 (en) | 1975-12-19 | 1980-01-31 | Societe D'etudes Et D'applications Techniques S.E.D.A.T., Irigny, Rhone (Frankreich) | Device comprising an acupuncture needle and a device for piercing the same |
DE2642896C3 (en) | 1976-09-24 | 1980-08-21 | 7800 Freiburg | Precision snapper for setting standard stab wounds in the skin for diagnostic purposes |
US4257561A (en) | 1979-06-05 | 1981-03-24 | Ethyl Products Company | Child-resistant dispensing nozzle assembly |
FR2487037B1 (en) | 1980-07-17 | 1986-02-21 | Vallourec | JOINT FOR TUBES INTENDED IN PARTICULAR FOR THE OIL INDUSTRY |
US4388925A (en) | 1981-03-23 | 1983-06-21 | Becton Dickinson And Company | Automatic retractable lancet assembly |
FR2508305B1 (en) | 1981-06-25 | 1986-04-11 | Slama Gerard | DEVICE FOR CAUSING A LITTLE BITE TO COLLECT A BLOOD DROP |
US4449529A (en) | 1981-11-18 | 1984-05-22 | Becton Dickinson And Company | Automatic retractable lancet assembly |
USRE32922E (en) | 1983-01-13 | 1989-05-16 | Paul D. Levin | Blood sampling instrument |
US4517978A (en) | 1983-01-13 | 1985-05-21 | Levin Paul D | Blood sampling instrument |
US4628929A (en) | 1985-08-16 | 1986-12-16 | American Hospital Supply Corporation | Retractable blade bleeding time device |
US4834667A (en) | 1986-02-24 | 1989-05-30 | Engineered Transitions Co., Inc. | Vibration resistant electrical coupling |
IT207944Z2 (en) | 1986-07-25 | 1988-03-14 | Erba Farmitalia | LOCKING DEVICE OF A SYRINGE ON A BODY TO WHICH THE SYRINGE MUST BE COUPLED. |
GB8710470D0 (en) | 1987-05-01 | 1987-06-03 | Mumford Ltd Owen | Blood sampling devices |
US4850973A (en) | 1987-10-16 | 1989-07-25 | Pavel Jordon & Associates | Plastic device for injection and obtaining blood samples |
US4924879A (en) | 1988-10-07 | 1990-05-15 | Brien Walter J O | Blood lancet device |
US4895147A (en) | 1988-10-28 | 1990-01-23 | Sherwood Medical Company | Lancet injector |
US4990154A (en) | 1989-06-19 | 1991-02-05 | Miles Inc. | Lancet assembly |
US4976724A (en) | 1989-08-25 | 1990-12-11 | Lifescan, Inc. | Lancet ejector mechanism |
US5147375A (en) | 1991-05-31 | 1992-09-15 | Ann Sullivan | Safety finger prick instrument |
US5284156A (en) | 1991-08-30 | 1994-02-08 | M3 Systems, Inc. | Automatic tissue sampling apparatus |
DE69229180T2 (en) | 1991-11-12 | 1999-10-14 | Urs A Ramel | LANCETTE DEVICE |
DE4212315A1 (en) | 1992-04-13 | 1993-10-14 | Boehringer Mannheim Gmbh | Blood lancet device for drawing blood for diagnostic purposes |
PL169210B1 (en) | 1992-08-03 | 1996-06-28 | Przed Zagraniczne Htl | Puncturing device |
CA2079192C (en) | 1992-09-25 | 1995-12-26 | Bernard Strong | Combined lancet and multi-function cap and lancet injector for use therewith |
US5269799A (en) | 1992-11-05 | 1993-12-14 | Daniel Richard F | Finger pricker |
US5282822A (en) | 1993-01-19 | 1994-02-01 | Sherwood Medical Company | Lancet ejector for lancet injector |
US5395388A (en) | 1993-11-15 | 1995-03-07 | Schraga; Steven | Single unit lancet device |
JP3393920B2 (en) | 1993-12-09 | 2003-04-07 | 富士写真フイルム株式会社 | Wearing equipment for small-volume fixed-volume blood sampling points |
US5464418A (en) | 1993-12-09 | 1995-11-07 | Schraga; Steven | Reusable lancet device |
US5439473A (en) | 1993-12-13 | 1995-08-08 | Modulohm A/S | Safety lancet |
US5509345A (en) | 1994-01-26 | 1996-04-23 | Cyktich; James M. | Muzzle attachment for improving firearm accuracy |
US5350392A (en) | 1994-02-03 | 1994-09-27 | Miles Inc. | Lancing device with automatic cocking |
US5454828A (en) | 1994-03-16 | 1995-10-03 | Schraga; Steven | Lancet unit with safety sleeve |
USD376203S (en) | 1994-10-31 | 1996-12-03 | Steven Schraga | Single use lancet |
US5628765A (en) | 1994-11-29 | 1997-05-13 | Apls Co., Ltd. | Lancet assembly |
US5518004A (en) | 1994-12-12 | 1996-05-21 | Schraga; Steven | Specimen drawing device |
US5628764A (en) | 1995-03-21 | 1997-05-13 | Schraga; Steven | Collar lancet device |
US5569286A (en) | 1995-03-29 | 1996-10-29 | Becton Dickinson And Company | Lancet assembly |
US5879367A (en) | 1995-09-08 | 1999-03-09 | Integ, Inc. | Enhanced interstitial fluid collection |
US5643306A (en) | 1996-03-22 | 1997-07-01 | Stat Medical Devices Inc. | Disposable lancet |
US6332871B1 (en) | 1996-05-17 | 2001-12-25 | Amira Medical | Blood and interstitial fluid sampling device |
WO1997042883A1 (en) | 1996-05-17 | 1997-11-20 | Mercury Diagnostics, Inc. | Disposable element for use in a body fluid sampling device |
US5741288A (en) | 1996-06-27 | 1998-04-21 | Chemtrak, Inc. | Re-armable single-user safety finger stick device having reset for multiple use by a single patient |
GB9619462D0 (en) | 1996-09-18 | 1996-10-30 | Owen Mumford Ltd | Improvements relating to lancet devices |
US5797942A (en) | 1996-09-23 | 1998-08-25 | Schraga; Steven | Re-usable end cap for re-usable lancet devices for removing and disposing of a contaminated lancet |
US5873887A (en) | 1996-10-25 | 1999-02-23 | Bayer Corporation | Blood sampling device |
US5984940A (en) | 1997-05-29 | 1999-11-16 | Atrion Medical Products, Inc. | Lancet device |
US6056765A (en) | 1997-06-24 | 2000-05-02 | Bajaj; Ratan | Lancet device |
US6221089B1 (en) | 1997-07-07 | 2001-04-24 | International Technidyne Corporation | Skin incision device with compression spring assembly |
US6071294A (en) | 1997-12-04 | 2000-06-06 | Agilent Technologies, Inc. | Lancet cartridge for sampling blood |
US5908434A (en) | 1998-02-13 | 1999-06-01 | Schraga; Steven | Lancet device |
US6346114B1 (en) | 1998-06-11 | 2002-02-12 | Stat Medical Devices, Inc. | Adjustable length member such as a cap of a lancet device for adjusting penetration depth |
US6022366A (en) | 1998-06-11 | 2000-02-08 | Stat Medical Devices Inc. | Lancet having adjustable penetration depth |
US6210420B1 (en) | 1999-01-19 | 2001-04-03 | Agilent Technologies, Inc. | Apparatus and method for efficient blood sampling with lancet |
USD428150S (en) | 1999-02-23 | 2000-07-11 | Lifescan, Inc. | Lancing device |
US6197040B1 (en) | 1999-02-23 | 2001-03-06 | Lifescan, Inc. | Lancing device having a releasable connector |
US6045567A (en) | 1999-02-23 | 2000-04-04 | Lifescan Inc. | Lancing device causing reduced pain |
US6306152B1 (en) | 1999-03-08 | 2001-10-23 | Agilent Technologies, Inc. | Lancet device with skin movement control and ballistic preload |
US6192891B1 (en) | 1999-04-26 | 2001-02-27 | Becton Dickinson And Company | Integrated system including medication delivery pen, blood monitoring device, and lancer |
US6152942A (en) | 1999-06-14 | 2000-11-28 | Bayer Corporation | Vacuum assisted lancing device |
US6168606B1 (en) | 1999-11-10 | 2001-01-02 | Palco Labs, Inc. | Single-use lancet device |
US6283982B1 (en) * | 1999-10-19 | 2001-09-04 | Facet Technologies, Inc. | Lancing device and method of sample collection |
US6228100B1 (en) | 1999-10-25 | 2001-05-08 | Steven Schraga | Multi-use lancet device |
CA2287757A1 (en) | 1999-10-29 | 2001-04-29 | Medical Plastic Devices M.P.D. Inc. | Disposable lancet |
US6258112B1 (en) | 1999-11-02 | 2001-07-10 | Steven Schraga | Single use lancet assembly |
US6322575B1 (en) | 2000-01-05 | 2001-11-27 | Steven Schraga | Lancet depth adjustment assembly |
EP1405595B2 (en) * | 2001-07-11 | 2010-09-01 | ARKRAY, Inc. | Piercing device |
-
2003
- 2003-08-15 US US10/641,101 patent/US7105006B2/en not_active Expired - Lifetime
-
2004
- 2004-08-13 CN CNB2004800303691A patent/CN100450451C/en not_active Expired - Fee Related
- 2004-08-13 EP EP04780835A patent/EP1663022A4/en not_active Withdrawn
- 2004-08-13 AU AU2004266638A patent/AU2004266638A1/en not_active Abandoned
- 2004-08-13 CA CA002535785A patent/CA2535785A1/en not_active Abandoned
- 2004-08-13 WO PCT/US2004/026060 patent/WO2005018421A2/en active Application Filing
Patent Citations (35)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2823677A (en) * | 1955-01-17 | 1958-02-18 | Becton Dickinson Co | Lancet |
US3760809A (en) * | 1971-10-22 | 1973-09-25 | Damon Corp | Surgical lancet having casing |
US4157086A (en) * | 1975-10-13 | 1979-06-05 | Farmitalia Carlo Erba S.P.A. | Apparatus for providing skin cuts to a predetermined measure |
US4064871A (en) * | 1976-05-11 | 1977-12-27 | Becton, Dickinson And Company | Device for making precise incisions for bleeding time testing and the like |
US4438770A (en) * | 1979-03-23 | 1984-03-27 | Hans Peter Olof Unger | Skin incising device |
US4553541A (en) * | 1981-03-23 | 1985-11-19 | Becton, Dickinson And Co. | Automatic retractable lancet assembly |
US4539988A (en) * | 1983-07-05 | 1985-09-10 | Packaging Corporation International | Disposable automatic lancet |
US6395495B1 (en) * | 1983-09-15 | 2002-05-28 | Institut Pasteur | Methods and kits for detecting antibodies against an HIV variant |
US4643189A (en) * | 1985-02-19 | 1987-02-17 | W. T. Associates | Apparatus for implementing a standardized skin incision |
US5196025A (en) * | 1990-05-21 | 1993-03-23 | Ryder International Corporation | Lancet actuator with retractable mechanism |
US5133730A (en) * | 1991-05-15 | 1992-07-28 | International Technidyne Corporation | Disposable-retractable finger stick device |
US5314441A (en) * | 1992-10-16 | 1994-05-24 | International Technidyne Corporation | Disposable slicing lancet assembly |
US5554166A (en) * | 1993-06-21 | 1996-09-10 | Boehringer Mannheim Gmbh | Blood lancet device for withdrawing blood for diagnostic purposes |
US5304193A (en) * | 1993-08-12 | 1994-04-19 | Sam Zhadanov | Blood lancing device |
US5545174A (en) * | 1994-01-11 | 1996-08-13 | Sherwood Medical Company | Finger stick device |
US5589156A (en) * | 1994-05-02 | 1996-12-31 | Henry; Richard A. | Prilocaine and hydrofluourocarbon aerosol preparations |
US5529581A (en) * | 1994-05-17 | 1996-06-25 | International Technidyne Corporation | Lancet device for creating a skin incision |
US5527334A (en) * | 1994-05-25 | 1996-06-18 | Ryder International Corporation | Disposable, retractable lancet |
US5527333A (en) * | 1994-09-09 | 1996-06-18 | Graphic Controls Corporation | Slicing disposable blood sampling device |
US5571132A (en) * | 1995-06-06 | 1996-11-05 | International Technidyne Corporation | Self activated finger lancet |
US5730753A (en) * | 1995-07-28 | 1998-03-24 | Apls Co., Ltd. | Assembly for adjusting pricking depth of lancet |
US5662672A (en) * | 1996-05-23 | 1997-09-02 | Array Medical, Inc. | Single use, bi-directional linear motion lancet |
US5733300A (en) * | 1996-05-23 | 1998-03-31 | Array Medical, Inc. | Single use, bi-directional linear motion lancet |
US5613978A (en) * | 1996-06-04 | 1997-03-25 | Palco Laboratories | Adjustable tip for lancet device |
US5772677A (en) * | 1996-09-24 | 1998-06-30 | International Technidyne Corporation | Incision device capable of automatic assembly and a method of assembly |
US6010519A (en) * | 1996-09-24 | 2000-01-04 | International Technidyne Corporation | Incision device capable of automatic assembly and a method of assembly |
US5797940A (en) * | 1997-05-30 | 1998-08-25 | International Technidyne Corporation | Adjustable skin incision device |
US5916230A (en) * | 1997-06-16 | 1999-06-29 | Bayer Corporation | Blood sampling device with adjustable end cap |
US6207184B1 (en) * | 1998-06-18 | 2001-03-27 | Ssp Co., Ltd. | Hydrophilic adhesive masses |
US6635674B1 (en) * | 1998-11-06 | 2003-10-21 | Bristol-Myers Squibb Co. | Pharmaceutical preparations for external use containing non-steroidal anti-inflammatory and analgesic agents |
US6042595A (en) * | 1999-03-02 | 2000-03-28 | Apls Co., Ltd. | Lancet apparatus for producing a precisely controlled incision |
US6558402B1 (en) * | 1999-08-03 | 2003-05-06 | Becton, Dickinson And Company | Lancer |
US20030187470A1 (en) * | 1999-08-03 | 2003-10-02 | Chelak Todd M. | Lancer |
US6358265B1 (en) * | 2000-07-18 | 2002-03-19 | Specialized Health Products, Inc. | Single-step disposable safety lancet apparatus and methods |
US20030028126A1 (en) * | 2001-05-05 | 2003-02-06 | Hans List | Blood withdrawal system |
Cited By (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8834503B2 (en) | 1998-06-11 | 2014-09-16 | Stat Medical Devices, Inc. | Lancet having adjustable penetration depth |
US8888804B2 (en) | 2003-08-15 | 2014-11-18 | Stat Medical Devices, Inc. | Adjustable lancet device and method |
US9375175B2 (en) | 2005-08-04 | 2016-06-28 | Ascensia Diabetes Care Holdings Ag | Lancing device |
US8864783B2 (en) | 2005-08-04 | 2014-10-21 | Bayer Healthcare Llc | Lancing device |
US8876846B2 (en) | 2005-11-03 | 2014-11-04 | Stat Medical Devices, Inc. | Disposable/single-use blade lancet device and method |
US20080077167A1 (en) * | 2006-06-15 | 2008-03-27 | Abbott Diabetes Care Inc. | Lancing Devices Having Depth Adjustment Assembly |
US7909842B2 (en) | 2006-06-15 | 2011-03-22 | Abbott Diabetes Care Inc. | Lancing devices having depth adjustment assembly |
US20080015503A1 (en) * | 2006-07-14 | 2008-01-17 | Roche Diagnostics Operations, Inc. | Injection device |
US7758545B2 (en) * | 2006-07-14 | 2010-07-20 | Roche Diagnostics Operations, Inc. | Injection device |
US20080195132A1 (en) * | 2007-02-08 | 2008-08-14 | Stat Medical Devices, Inc. | Push-button lance device and method |
US8043318B2 (en) | 2007-02-08 | 2011-10-25 | Stat Medical Devices, Inc. | Push-button lance device and method |
WO2008121680A3 (en) * | 2007-03-30 | 2008-12-11 | Stat Medical Devices Inc | Lancet device with combined trigger and cocking mechanism and method |
US8469986B2 (en) | 2007-03-30 | 2013-06-25 | Stat Medical Devices, Inc. | Lancet device with combined trigger and cocking mechanism and method |
US9307939B2 (en) | 2007-03-30 | 2016-04-12 | Stat Medical Devices, Inc. | Lancet device with combined trigger and cocking mechanism |
WO2008121680A2 (en) * | 2007-03-30 | 2008-10-09 | Stat Medical Devices, Inc. | Lancet device with combined trigger and cocking mechanism and method |
US8029526B2 (en) | 2008-08-14 | 2011-10-04 | Abbott Diabetes Care Inc. | Cocking mechanism for lancing device |
US20100042131A1 (en) * | 2008-08-14 | 2010-02-18 | Abbott Diabetes Care Inc. | Cocking mechanism for lancing device |
US20160106349A1 (en) * | 2012-04-04 | 2016-04-21 | Dexcom, Inc. | Transcutaneous analyte sensors, applicators therefor, and associated methods |
US11304631B2 (en) * | 2012-04-04 | 2022-04-19 | Dexcom, Inc. | Transcutaneous analyte sensors, applicators therefor, and associated methods |
Also Published As
Publication number | Publication date |
---|---|
US7105006B2 (en) | 2006-09-12 |
WO2005018421A2 (en) | 2005-03-03 |
EP1663022A2 (en) | 2006-06-07 |
AU2004266638A1 (en) | 2005-03-03 |
WO2005018421A3 (en) | 2005-09-15 |
EP1663022A4 (en) | 2009-03-04 |
CN1867296A (en) | 2006-11-22 |
CA2535785A1 (en) | 2005-03-03 |
CN100450451C (en) | 2009-01-14 |
US20050038464A1 (en) | 2005-02-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US7105006B2 (en) | Adjustable lancet device and method | |
US7621931B2 (en) | Adjustable lancet device and method | |
US8257380B2 (en) | Adjustabable disposable/single-use lancet device and method | |
US8888804B2 (en) | Adjustable lancet device and method | |
US9307939B2 (en) | Lancet device with combined trigger and cocking mechanism | |
US8043318B2 (en) | Push-button lance device and method | |
US7909842B2 (en) | Lancing devices having depth adjustment assembly | |
EP1261287B1 (en) | Adjustable tip for a lancet device | |
US20070083222A1 (en) | Lancet device, removal system for lancet device, and method | |
US20160007898A1 (en) | Lancet device with depth adjustment and lancet removal system and method | |
JP3697100B2 (en) | Puncture tool |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: STAT MEDICAL DEVICES, INC., FLORIDA Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:SCHRAGA, STEVEN;REEL/FRAME:014396/0728 Effective date: 20030808 |
|
FEPP | Fee payment procedure |
Free format text: PETITION RELATED TO MAINTENANCE FEES FILED (ORIGINAL EVENT CODE: PMFP); ENTITY STATUS OF PATENT OWNER: SMALL ENTITY Free format text: PETITION RELATED TO MAINTENANCE FEES GRANTED (ORIGINAL EVENT CODE: PMFG); ENTITY STATUS OF PATENT OWNER: SMALL ENTITY |
|
REMI | Maintenance fee reminder mailed | ||
REIN | Reinstatement after maintenance fee payment confirmed | ||
PRDP | Patent reinstated due to the acceptance of a late maintenance fee |
Effective date: 20101105 |
|
FP | Lapsed due to failure to pay maintenance fee |
Effective date: 20100912 |
|
FPAY | Fee payment |
Year of fee payment: 4 |
|
SULP | Surcharge for late payment | ||
CC | Certificate of correction | ||
FEPP | Fee payment procedure |
Free format text: PETITION RELATED TO MAINTENANCE FEES GRANTED (ORIGINAL EVENT CODE: PMFG); ENTITY STATUS OF PATENT OWNER: SMALL ENTITY Free format text: PETITION RELATED TO MAINTENANCE FEES FILED (ORIGINAL EVENT CODE: PMFP); ENTITY STATUS OF PATENT OWNER: SMALL ENTITY |
|
REMI | Maintenance fee reminder mailed | ||
LAPS | Lapse for failure to pay maintenance fees | ||
REIN | Reinstatement after maintenance fee payment confirmed | ||
PRDP | Patent reinstated due to the acceptance of a late maintenance fee |
Effective date: 20141029 |
|
FPAY | Fee payment |
Year of fee payment: 8 |
|
STCF | Information on status: patent grant |
Free format text: PATENTED CASE |
|
FP | Lapsed due to failure to pay maintenance fee |
Effective date: 20140912 |
|
MAFP | Maintenance fee payment |
Free format text: PAYMENT OF MAINTENANCE FEE, 12TH YR, SMALL ENTITY (ORIGINAL EVENT CODE: M2553) Year of fee payment: 12 |