US20150041496A1 - Single use enhancement for dispenser assembly - Google Patents

Single use enhancement for dispenser assembly Download PDF

Info

Publication number
US20150041496A1
US20150041496A1 US13/962,007 US201313962007A US2015041496A1 US 20150041496 A1 US20150041496 A1 US 20150041496A1 US 201313962007 A US201313962007 A US 201313962007A US 2015041496 A1 US2015041496 A1 US 2015041496A1
Authority
US
United States
Prior art keywords
plunger
dispenser assembly
recited
disposed
locking device
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.)
Abandoned
Application number
US13/962,007
Inventor
Sungmoon Kim
Bonggeun Kim
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Aptar France SAS
Original Assignee
Individual
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to US13/962,007 priority Critical patent/US20150041496A1/en
Assigned to APTAR FRANCE SAS reassignment APTAR FRANCE SAS ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: KIM, Bonggeun, KIM, Sungmoon
Priority to PCT/EP2014/066925 priority patent/WO2015018869A1/en
Publication of US20150041496A1 publication Critical patent/US20150041496A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M15/00Inhalators
    • A61M15/0028Inhalators using prepacked dosages, one for each application, e.g. capsules to be perforated or broken-up
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B65CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
    • B65DCONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
    • B65D83/00Containers or packages with special means for dispensing contents
    • B65D83/0005Containers or packages provided with a piston or with a movable bottom or partition having approximately the same section as the container
    • B65D83/0033Containers or packages provided with a piston or with a movable bottom or partition having approximately the same section as the container the piston being a follower-piston and the dispensing means comprising a hand-operated pressure-device at the opposite part of the container
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M11/00Sprayers or atomisers specially adapted for therapeutic purposes
    • A61M11/006Sprayers or atomisers specially adapted for therapeutic purposes operated by applying mechanical pressure to the liquid to be sprayed or atomised
    • A61M11/007Syringe-type or piston-type sprayers or atomisers
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M15/00Inhalators
    • A61M15/0065Inhalators with dosage or measuring devices
    • A61M15/0068Indicating or counting the number of dispensed doses or of remaining doses
    • A61M15/0081Locking means
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M15/00Inhalators
    • A61M15/08Inhaling devices inserted into the nose
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2205/00General characteristics of the apparatus
    • A61M2205/27General characteristics of the apparatus preventing use
    • A61M2205/273General characteristics of the apparatus preventing use preventing reuse, e.g. of disposables

Definitions

  • This invention is directed to a locking device structured for use in combination with a dispenser assembly and including the structural versatility enabling it to be an original part of the dispensing assembly when manufactured and assembled or as an add-on device.
  • the locking device is structured to assume a movement restricting engagement with an activating plunger of the dispenser assembly thereby assuring that the dispenser assembly will be used and operated as a “single-use” device.
  • Dispenser assemblies structured to dispense medical or therapeutic compositions into the nasal passages of an individual are common and used extensively for the treatment of nasal and sinus conditions.
  • One typical structure for this type of dispenser is known as a “squeeze” bottle, wherein resilient walls of the dispenser structure are manually compressed, resulting in a mixture of air and intended medication being directed from the discharge nozzle thereof.
  • a dispenser of this type is intended for repeated use, thereby rendering it difficult to control the amount of composition delivered.
  • there is a tendency, after discharge, to release the resilient walls of the squeeze type dispenser which in turn results in an inadvertent withdrawal of fluids from the nasal passage.
  • Such fluids typically will accumulate on the exterior surface of the nozzle.
  • multiple users of the same dispenser assembly are in danger of infection by coming in contact with or inhaling the bodily fluids accumulated from the last user or previous users.
  • single-dose administration devices are sometimes preferred for a variety of reasons including dose precision and prevention of transmission of infection/reduction of risk of contamination. More specifically, depending on the structural and/or operative features of the administration device, it may be obvious that the dose has been dispensed and that it no longer has any medication in it. However, for other designs it may be difficult or indeed impossible to know if the device has been used or not. Such situations may occur if the administration device does not preclude the operative positioning of an activating member such as, but not limited to, the withdrawal of an activating “plunger” or like component. As a result a discharge device may appear to be identical to a device which has not been discharged.
  • dispenser assemblies specifically including, but not limited to, nasal or other dispenser structures intended to deliver a therapeutic or medicinal composition, for an improved dispenser assembly.
  • Such an improved dispenser structure should be operative to overcome problems and disadvantages of the type set forth above.
  • one proposed and improved dispenser assembly can be initially structured and/or subsequently modified to operate as a “single-use” dispenser.
  • the operative components of such an improved dispenser assembly would become inoperable at least to the extent of preventing its re-use thereby limiting the quantity of material that may be dispensed therefrom.
  • single-use dispensers overcome many of the problems of the type set forth above by allowing only a single dose to be dispensed.
  • the chances of infections being transferred from one individual to another is eliminated or significantly reduced.
  • a single-use structuring of a dispenser assembly may involve the inclusion of an improved locking device.
  • the structural and operative features of such an improved locking device facilitates its use as an original component of a dispenser assembly as manufactured and assembled (OEM) or alternatively serve as an “add-on” component to a dispenser assembly which has already been designed and manufactured.
  • Structural and operative features of such a proposed and improved locking device would enable the normal operation of other components of the dispenser assembly such as, but not limited to, an activating plunger movable into a dispensed orientation to facilitate the dispensing of a single dose material from the dispenser assembly.
  • the proposed and improved locking device would also serve to interact with the plunger assembly or other operative components of the dispenser assembly to prevent a re-use thereof and/or more than one, predetermined doses being dispensed therefrom.
  • the present invention is directed to a locking device which is structured to be used in combination with a dispenser assembly, either as part of its original manufactured components (OEM) or as an “add-on” included after the other components of the dispensed assembly have been designed and manufactured.
  • the locking device of the present invention renders the dispenser assembly a “single-use” device by preventing or at least restricting an activating plunger of the dispenser assembly from being disposed back into an operative or “ready” position from an inoperative or dispensed position, once a single dispensing cycle has occurred.
  • the dispenser assembly as described and represented herein may be considered only representative of other dispenser assemblies having different structural and operative features.
  • the representative dispenser assembly referred to herein includes a housing, a dispensing portion, an activating plunger, and a supply of material and/or composition intended to be dispensed.
  • the locking device of the present invention comprises a body dimensioned and configured to be disposed on an interior of the housing of the dispensing assembly in an accessible, engaging relation to the plunger, as the plunger moves from the aforementioned operative or “ready” position into the inoperative or “dispensed” position.
  • the body includes an open and/or hollow interior having oppositely disposed open ends.
  • the body includes a substantially cylindrically configured outer wall disposed in surrounding relation to the open interior and at least partially defining the boundaries thereof.
  • the inner or proximal open end of the body includes a head portion extending transversely outward, about the periphery thereof and includes an outer exposed surface.
  • a connector disposed in securing position between the outer or exposed surface of the head of the body and correspondingly disposed interior surface portions of the housing dispenser.
  • a connector may be at least partially formed of an adhesive material thereby serving to adhesively secure the body of the locking device in its intended position.
  • the body includes a locking structure formed thereon.
  • the cylindrical outer wall of the body includes a locking flange connected to the exterior outer wall and extending outwardly therefrom preferably, but not necessarily at an upwardly directed angular orientation.
  • the dimension and configuration of the locking flange will be such as to purposefully interfere with passage and movement of the plunger by sliding but frictionally engaging corresponding portions of the activating plunger as it is selectively forced from the operative, ready position into the inoperative, dispensed position. Once disposed in the dispensed or inoperative position, the frictional engagement between the locking flange of the locking structure and corresponding surface portions of the activating plunger will define a movement restricting engagement therebetween.
  • activating plunger will be prevented from moving back into the operative or ready-to-use position after a single dispensing cycle of the dispenser assembly has occurred.
  • maintaining the activating plunger in the inoperative or dispensed position prevents its re-use.
  • locking device of the present invention may include the locking flange of the locking structure being at least partially flexible, being formed of a relatively flexible material and/or having at least a minimal amount of flexibility due to its interconnection with the outer wall of the body.
  • the locking flange of the locking structure being at least partially flexible, being formed of a relatively flexible material and/or having at least a minimal amount of flexibility due to its interconnection with the outer wall of the body.
  • the locking device demonstrates sufficient structural versatility to be considered an original component of the dispenser assembly as it is manufactured and assembled.
  • the locking structure may be an add-on device so as to assure that the dispenser assembly operates as a single use dispenser.
  • the dispenser assembly itself may be structured to dispense a variety of different materials and/or be specifically customized or structured as to serve as a single purpose dispenser such as nasal dispenser.
  • the dispensing portion of the dispenser assembly may be at least partially dimensioned or configured to facilitate specified dispensing procedures, such as including a dispensing nozzle.
  • the locking device of the present invention is operatively structured with both the dispensing portion of the dispenser assembly as well as the plunger so as to not interfere with movement or positioning of the plunger into operative relation with the dispensing portion and supply of material to be dispensed.
  • the open interior configuration of the body as well as the oppositely disposed open ends thereof are disposed and dimensioned to facilitate the normal or intended operation of the plunger as it interacts with the dispensing portion of the dispenser assembly when the plunger is forced from the ready or operative position to the dispensed or inoperative position.
  • the aforementioned locking structure at least partially defined by the locking flange will prevent return movement of the plunger from the inoperative, dispensed position back into the operative, ready position.
  • FIG. 1 is a perspective view of a locking device to be operatively positioned within the interior of a dispenser assembly thereby facilitating its use as a single-use dispenser.
  • FIG. 1A is a perspective view of a connector used to connect the locking device of the embodiment of FIG. 1 within the interior of the dispensed assembly.
  • FIG. 2 is a longitudinal sectional view showing interior portions of an example of a dispenser assembly with which the locking device of the embodiment of FIG. 1 may be used.
  • FIG. 3 is a detailed view in partial cutaway of the indicated portion of FIG. 2 .
  • FIG. 4 is an interior sectional view in the partial cutaway of the embodiments of FIGS. 1-3 in an operative position.
  • FIG. 5 is an interior sectional view in partial cutaway of the embodiment of FIG. 4 in an at least partially dispensed position.
  • FIG. 6 is an interior sectional view of the embodiment of FIGS. 1-5 in a non-operative position upon completion of the dispensing of the material from the dispensing assembly.
  • FIG. 7 is a detailed view of the indicated portion of FIG. 6 .
  • the present invention is directed to a locking device generally indicated as 10 structured to be used in combination with a dispenser assembly of the type represented in FIG. 2 and generally represented as 12 .
  • a dispenser assembly of the type represented in FIG. 2 and generally represented as 12 .
  • the dispenser assembly 12 is represented in example form only in that structural features of a different dispenser assembly (not shown) may vary from the dispenser assembly 12 and still be operative when used in combination with the locking device 10 .
  • the dispenser assembly 12 includes a housing 14 and a dispensing portion generally indicated as 16 connected thereto or otherwise associated therewith.
  • the dispensing portion 16 is operatively associated with a material or composition (not shown) intended to be dispensed.
  • the dispenser assembly 12 also includes a delivery portion 18 which may be in the form of a nozzle or like structure such as, but not limited to, the type intended to deliver medicinal or therapeutic material to nasal passages of an individual.
  • the delivery portion or nozzle 18 may be appropriately shaped for at least minimal insertion into the nostril and/or nasal passages of the individuals, but is not limited to such a use or application.
  • a plunger generally indicated as 20 , which serves to engage and activate the dispensing portion 16 as it moves from an operative or “ready” position of FIG. 2 into a “dispensed” or inoperative position as represented in FIG. 6 .
  • the plunger in the embodiment represented in FIG. 2 has an activating member 22 disposable into activating and/or operative engagement with a portion of a dispensing assembly 16 so as to cause the dispensing of the intended material from the dispensing portion 16 and delivery portion or nozzle 18 .
  • the activating member or portion 22 moves with the plunger 20 as it is forced within the interior of the body 14 , such that the activating member or portion 22 engages the dispensing portion 16 in an intended manner. Therefore and as indicated above, in the operative or ready position of FIG. 2 the plunger extends outwardly from the body 14 in a “non-activating” engagement or relation to the dispensing portion 16 .
  • the activating member 22 associated with the plunger 20 moves into activating engagement with the dispensing portion 16 as the plunger 20 progressively passes through the interior of the housing 14 in the manner represented in FIGS. 5 and 6 .
  • the locking device 10 includes a body 30 preferably comprising a substantially cylindrical outer wall configuration and an open interior including oppositely disposed open ends 32 and 34 .
  • the body 30 also includes a head portion generally indicated as 36 comprising a connecting flange 38 having an outer exposed surface 38 ′ which is dimensioned and configured to facilitate secure connection or mounting of the locking device 10 within the interior of the housing 14 of the dispenser assembly 12 .
  • the connecting flange 38 extends transversely outward from the body 30 in at least partially surrounding relation to the open end 34 and/or the periphery thereof.
  • a connector generally indicated as 40 is dimensioned and configured to be at least partially mounted on the outer surface 38 ′ of the connecting flange 38 .
  • the connecting flange 38 serves to interconnect the body 30 to correspondingly disposed interior portions, as at 42 , of the housing 14 .
  • at least one embodiment of the connector 40 may include a substantially annular configuration at least partially corresponding to the annular configuration of the connecting flange 38 and outer exposed surface 38 ′.
  • the connector 40 may be at least partially formed from an adhesive material or have adhesive characteristics sufficient to adhesively interconnect the mounting flange 38 and accordingly the remainder of the body 30 to interior surface portions or other corresponding portions 42 within the housing 14 .
  • the locking device 10 may be operatively mounted and/or connected within the interior of the housing 14 and as such may be an original component of the dispenser assembly 12 as it is initially manufactured, produced and/or assembled.
  • the structural versatility of the locking device 10 enables it to be added to a dispenser assembly 12 , of the type represented in FIG. 2 , as an “add-on” component.
  • the locking device 10 is structured to facilitate the original manufacture or the conversion of a dispenser assembly 12 to a “single-use” dispenser. In doing so, many of the disadvantages and problems recognized in the structural and operative features of known devices of this type are overcome. As set forth herein such problems include, but are not limited to, the monitoring or regulating of the individual dose of material being dispensed from the dispenser assembly 12 .
  • the structural and operative features of the locking device 10 which enables the operation and use of a dispenser assembly 12 as a “single-use” dispenser includes the provision of a locking structure generally indicated as 46 .
  • the locking structure 46 preferably comprises a locking structure 46 in the form of locking flange 48 .
  • the locking structure and locking flange 48 is connected exteriorly of the body 30 to the outer cylindrical wall 30 ′ preferably, but not necessarily, adjacent or contiguous to a corresponding end 32 .
  • the locking flange 48 due at least in part to the material from which it is formed or alternatively due to its connection to the body 30 , is at least partially flexible and/or demonstrates flexible characteristics.
  • the maintenance of the plunger 20 in the non-operative and/or dispensed position renders the dispenser assembly 12 a single-use device. This is accomplished by the locking flange 48 frictionally engaging and possibly at least minimally penetrating corresponding interior surfaces as at 21 ′ as clearly represented in FIGS. 6 and 7 .
  • the activating member 22 will operatively engage the dispensing portion 16 causing the dispensing of the intended material from the delivery portion or nozzle 18 , as intended.
  • the forced inward travel of the plunger 20 will also result in the interior surface portions 21 passing into sliding, frictional engagement with the locking flange 48 defining the locking structure 46 . Therefore, as represented in FIGS. 6 and 7 , at least the outer free end or periphery 48 ′ of the locking flange 48 will slidingly engage the correspondingly disposed interior surfaces 21 of the plunger 20 resulting in a frictional engagement therebetween.
  • the locking flange 48 may be forced or “biased” inwardly towards the outer cylindrical wall 30 ′. Due to the flexible characteristics of the locking flange 48 as well as the material from which it is formed, the locking flange 48 will be normally biased outwardly into the orientation or position represented in FIG. 2 , when the locking flange 48 is not engaged by the plunger 20 , as at plunger portion or surface 21 . However, once frictional engagement occurs between the interior surfaces 21 and the plunger 20 the locking flange 48 , the locking flange 48 will be at least partially biased inwardly towards the outer cylindrical wall 30 ′. This biased, frictional engagement may result in at least minimal embedding, scraping, penetrating, etc. of the outer free periphery 48 ′ into the interior surfaces 21 , as at 21 ′, of the plunger 20 as at least partially represented in FIGS. 6 and 7 .
  • the plunger 20 will be maintained into a movement restricting engagement with the locking flange 48 of the locking structure 46 and/or the outer free peripheral end 48 ′.
  • the plunger 20 will thereby be prevented from being returned to the operative or ready position as represented in FIGS. 2 and 4 .
  • the provision of the locking device 10 and its interactive movement restricting engagement with the interior surfaces 21 of the plunger 20 will thereby render the dispenser assembly 12 , with which the locking device 10 is used, as a “single-use” dispenser, as set forth above.
  • the locking device 10 includes the open interior of the body 10 and the direct communication of the open ends 32 and 34 therewith.
  • the locking device 10 including the body 30 can be said to be operatively mounted in at least partially surrounding relation to the dispensing portion 16 of the dispenser assembly 12 as clearly represented throughout the Figures.
  • the opened distal end 32 of the body 30 allows passage of the activating member 22 of the plunger 20 into activating or operative engagement with the dispensing portion 16 of the dispenser assembly 12 as clearly represented in FIGS. 5 through 7 . Therefore, the open interior of the body 30 of the locking device 10 can be said to be in receiving relation to the plunger 20 or at least the activating portion 22 thereof when the plunger 20 is forced into the dispensed position as clearly represented in FIG.
  • the body 30 and the outer cylindrical wall 30 ′ can also be said to be in at least partially surrounding relation with both the dispensing portion 16 as well as the activating portion 22 of the plunger 20 .

Abstract

A locking device structured to maintain an activating plunger of a dispenser assembly in an inoperative position, subsequent to dispensing, so as to facilitate a single-use operation thereof and thereby preclude the potential confusion between a used and an unused single-use dispensing device. The locking device includes a body disposed in receiving relation to the plunger as it moves from an operative position to an inoperative position. A locking structure connected to the body is disposed to frictionally engage the plunger in movement restricting relation during its passage from the operative position to the inoperative position. Such frictional engagement is sufficient to restrict movement of the plunger back into the operative position once the material has been dispensed.

Description

    BACKGROUND OF THE INVENTION
  • 1. Field of the Invention
  • This invention is directed to a locking device structured for use in combination with a dispenser assembly and including the structural versatility enabling it to be an original part of the dispensing assembly when manufactured and assembled or as an add-on device. In either application, the locking device is structured to assume a movement restricting engagement with an activating plunger of the dispenser assembly thereby assuring that the dispenser assembly will be used and operated as a “single-use” device.
  • 2. Description of the Related Art
  • Dispenser assemblies structured to dispense medical or therapeutic compositions into the nasal passages of an individual are common and used extensively for the treatment of nasal and sinus conditions. One typical structure for this type of dispenser is known as a “squeeze” bottle, wherein resilient walls of the dispenser structure are manually compressed, resulting in a mixture of air and intended medication being directed from the discharge nozzle thereof. Typically, a dispenser of this type is intended for repeated use, thereby rendering it difficult to control the amount of composition delivered. In addition, there is a tendency, after discharge, to release the resilient walls of the squeeze type dispenser which in turn results in an inadvertent withdrawal of fluids from the nasal passage. Such fluids typically will accumulate on the exterior surface of the nozzle. As a result multiple users of the same dispenser assembly are in danger of infection by coming in contact with or inhaling the bodily fluids accumulated from the last user or previous users.
  • In addition the operation and structure of many dispensers do not provide a meaningful control of the dose or amount of therapeutic composition being dispensed. As a result, the dose regimen for each dispenser cannot be controlled and may result in problems, disadvantages and harm to the user.
  • Accordingly, single-dose administration devices are sometimes preferred for a variety of reasons including dose precision and prevention of transmission of infection/reduction of risk of contamination. More specifically, depending on the structural and/or operative features of the administration device, it may be obvious that the dose has been dispensed and that it no longer has any medication in it. However, for other designs it may be difficult or indeed impossible to know if the device has been used or not. Such situations may occur if the administration device does not preclude the operative positioning of an activating member such as, but not limited to, the withdrawal of an activating “plunger” or like component. As a result a discharge device may appear to be identical to a device which has not been discharged. Accordingly, in the latter scenario, a person may not recognize the medication dispenser has been used until after they try to use it. In the case of a medicine that is needed for emergency purposes, this could be extremely dangerous. Therefore, a mechanism that ensures a “used” single-use device could not be “reused” and would therefore not be confused with an “unused” single use device.
  • Therefore, there is a need in the art relating to dispenser assemblies specifically including, but not limited to, nasal or other dispenser structures intended to deliver a therapeutic or medicinal composition, for an improved dispenser assembly. Such an improved dispenser structure should be operative to overcome problems and disadvantages of the type set forth above. Accordingly one proposed and improved dispenser assembly can be initially structured and/or subsequently modified to operate as a “single-use” dispenser. As such, the operative components of such an improved dispenser assembly would become inoperable at least to the extent of preventing its re-use thereby limiting the quantity of material that may be dispensed therefrom. As should be apparent, single-use dispensers overcome many of the problems of the type set forth above by allowing only a single dose to be dispensed. In addition due to the fact that a dispenser assembly cannot be re-used, the chances of infections being transferred from one individual to another is eliminated or significantly reduced.
  • Moreover, a single-use structuring of a dispenser assembly may involve the inclusion of an improved locking device. Further, the structural and operative features of such an improved locking device facilitates its use as an original component of a dispenser assembly as manufactured and assembled (OEM) or alternatively serve as an “add-on” component to a dispenser assembly which has already been designed and manufactured. Structural and operative features of such a proposed and improved locking device would enable the normal operation of other components of the dispenser assembly such as, but not limited to, an activating plunger movable into a dispensed orientation to facilitate the dispensing of a single dose material from the dispenser assembly. However, the proposed and improved locking device would also serve to interact with the plunger assembly or other operative components of the dispenser assembly to prevent a re-use thereof and/or more than one, predetermined doses being dispensed therefrom.
  • Finally an improved and proposed locking device of the type needed to overcome the problems and disadvantages as set forth above would be of simple structure and design and would significantly reduce the cost thereof thereby facilitating its use in a single-use dispenser assembly which may thereafter be discarded.
  • SUMMARY OF THE INVENTION
  • The present invention is directed to a locking device which is structured to be used in combination with a dispenser assembly, either as part of its original manufactured components (OEM) or as an “add-on” included after the other components of the dispensed assembly have been designed and manufactured. In either application, the locking device of the present invention renders the dispenser assembly a “single-use” device by preventing or at least restricting an activating plunger of the dispenser assembly from being disposed back into an operative or “ready” position from an inoperative or dispensed position, once a single dispensing cycle has occurred.
  • Accordingly, the dispenser assembly, as described and represented herein may be considered only representative of other dispenser assemblies having different structural and operative features. As such, the representative dispenser assembly referred to herein includes a housing, a dispensing portion, an activating plunger, and a supply of material and/or composition intended to be dispensed.
  • More specifically, the locking device of the present invention comprises a body dimensioned and configured to be disposed on an interior of the housing of the dispensing assembly in an accessible, engaging relation to the plunger, as the plunger moves from the aforementioned operative or “ready” position into the inoperative or “dispensed” position. In at least one preferred embodiment, the body includes an open and/or hollow interior having oppositely disposed open ends. Further, the body includes a substantially cylindrically configured outer wall disposed in surrounding relation to the open interior and at least partially defining the boundaries thereof. The inner or proximal open end of the body includes a head portion extending transversely outward, about the periphery thereof and includes an outer exposed surface. Fixed positioning and secure mounting of the body within the interior of the housing of the dispenser assembly is facilitated through the provision of a connector disposed in securing position between the outer or exposed surface of the head of the body and correspondingly disposed interior surface portions of the housing dispenser. In at least one embodiment a connector may be at least partially formed of an adhesive material thereby serving to adhesively secure the body of the locking device in its intended position.
  • In addition, the body includes a locking structure formed thereon. In at least one preferred embodiment the cylindrical outer wall of the body includes a locking flange connected to the exterior outer wall and extending outwardly therefrom preferably, but not necessarily at an upwardly directed angular orientation. The dimension and configuration of the locking flange will be such as to purposefully interfere with passage and movement of the plunger by sliding but frictionally engaging corresponding portions of the activating plunger as it is selectively forced from the operative, ready position into the inoperative, dispensed position. Once disposed in the dispensed or inoperative position, the frictional engagement between the locking flange of the locking structure and corresponding surface portions of the activating plunger will define a movement restricting engagement therebetween. As a result, activating plunger will be prevented from moving back into the operative or ready-to-use position after a single dispensing cycle of the dispenser assembly has occurred. As should be evident, maintaining the activating plunger in the inoperative or dispensed position prevents its re-use.
  • Other structural and operative features of the locking device of the present invention may include the locking flange of the locking structure being at least partially flexible, being formed of a relatively flexible material and/or having at least a minimal amount of flexibility due to its interconnection with the outer wall of the body. As such passage of the activating plunger into the dispensed or inoperative position will force corresponding interior surfaces of the activating plunger into a sliding, frictional engagement with the outwardly extending locking flange of the locking structure. When such engagement occurs, the locking flange may be flexed inwardly towards the outer wall of the body to which it is attached.
  • As a result the frictional engagement between the locking flange and the corresponding surface of the plunger will be enhanced and maintained in that the flexible characteristics of the locking flange will tend to bias it outwardly into the aforementioned frictional, movement restricting engagement. As a result, the movement of the plunger back into the operative or ready position will be restricted or prevented, thereby making the dispenser assembly a “single-use” device. As set forth above, the locking device demonstrates sufficient structural versatility to be considered an original component of the dispenser assembly as it is manufactured and assembled. In contrast, the locking structure may be an add-on device so as to assure that the dispenser assembly operates as a single use dispenser.
  • Moreover, the dispenser assembly itself may be structured to dispense a variety of different materials and/or be specifically customized or structured as to serve as a single purpose dispenser such as nasal dispenser. In such a latter application, the dispensing portion of the dispenser assembly may be at least partially dimensioned or configured to facilitate specified dispensing procedures, such as including a dispensing nozzle. In addition, the locking device of the present invention is operatively structured with both the dispensing portion of the dispenser assembly as well as the plunger so as to not interfere with movement or positioning of the plunger into operative relation with the dispensing portion and supply of material to be dispensed. Therefore, the open interior configuration of the body as well as the oppositely disposed open ends thereof are disposed and dimensioned to facilitate the normal or intended operation of the plunger as it interacts with the dispensing portion of the dispenser assembly when the plunger is forced from the ready or operative position to the dispensed or inoperative position. However, the aforementioned locking structure at least partially defined by the locking flange will prevent return movement of the plunger from the inoperative, dispensed position back into the operative, ready position.
  • These and other objects, features and advantages of the present invention will become clearer when the drawings as well as the detailed description are taken into consideration.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • For a fuller understanding of the nature of the present invention, reference should be had to the following detailed description taken in connection with the accompanying drawings in which:
  • FIG. 1 is a perspective view of a locking device to be operatively positioned within the interior of a dispenser assembly thereby facilitating its use as a single-use dispenser.
  • FIG. 1A is a perspective view of a connector used to connect the locking device of the embodiment of FIG. 1 within the interior of the dispensed assembly.
  • FIG. 2 is a longitudinal sectional view showing interior portions of an example of a dispenser assembly with which the locking device of the embodiment of FIG. 1 may be used.
  • FIG. 3 is a detailed view in partial cutaway of the indicated portion of FIG. 2.
  • FIG. 4 is an interior sectional view in the partial cutaway of the embodiments of FIGS. 1-3 in an operative position.
  • FIG. 5 is an interior sectional view in partial cutaway of the embodiment of FIG. 4 in an at least partially dispensed position.
  • FIG. 6 is an interior sectional view of the embodiment of FIGS. 1-5 in a non-operative position upon completion of the dispensing of the material from the dispensing assembly.
  • FIG. 7 is a detailed view of the indicated portion of FIG. 6.
  • Like reference numerals refer to like parts throughout the several views of the drawings.
  • DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
  • As represented in the accompanying drawings, the present invention is directed to a locking device generally indicated as 10 structured to be used in combination with a dispenser assembly of the type represented in FIG. 2 and generally represented as 12. It is emphasized that the dispenser assembly 12 is represented in example form only in that structural features of a different dispenser assembly (not shown) may vary from the dispenser assembly 12 and still be operative when used in combination with the locking device 10.
  • Accordingly the dispenser assembly 12 includes a housing 14 and a dispensing portion generally indicated as 16 connected thereto or otherwise associated therewith. The dispensing portion 16 is operatively associated with a material or composition (not shown) intended to be dispensed. The dispenser assembly 12 also includes a delivery portion 18 which may be in the form of a nozzle or like structure such as, but not limited to, the type intended to deliver medicinal or therapeutic material to nasal passages of an individual. The delivery portion or nozzle 18 may be appropriately shaped for at least minimal insertion into the nostril and/or nasal passages of the individuals, but is not limited to such a use or application. Additional operative features of the dispenser assembly 12 include a plunger generally indicated as 20, which serves to engage and activate the dispensing portion 16 as it moves from an operative or “ready” position of FIG. 2 into a “dispensed” or inoperative position as represented in FIG. 6.
  • Dependent upon the specific cooperative structuring of the various components of the dispenser assembly 12, the plunger in the embodiment represented in FIG. 2 has an activating member 22 disposable into activating and/or operative engagement with a portion of a dispensing assembly 16 so as to cause the dispensing of the intended material from the dispensing portion 16 and delivery portion or nozzle 18. Accordingly, the activating member or portion 22 moves with the plunger 20 as it is forced within the interior of the body 14, such that the activating member or portion 22 engages the dispensing portion 16 in an intended manner. Therefore and as indicated above, in the operative or ready position of FIG. 2 the plunger extends outwardly from the body 14 in a “non-activating” engagement or relation to the dispensing portion 16. In contrast, the activating member 22 associated with the plunger 20 moves into activating engagement with the dispensing portion 16 as the plunger 20 progressively passes through the interior of the housing 14 in the manner represented in FIGS. 5 and 6.
  • With primary reference to FIG. 1, the locking device 10 includes a body 30 preferably comprising a substantially cylindrical outer wall configuration and an open interior including oppositely disposed open ends 32 and 34. The body 30 also includes a head portion generally indicated as 36 comprising a connecting flange 38 having an outer exposed surface 38′ which is dimensioned and configured to facilitate secure connection or mounting of the locking device 10 within the interior of the housing 14 of the dispenser assembly 12. As represented, the connecting flange 38 extends transversely outward from the body 30 in at least partially surrounding relation to the open end 34 and/or the periphery thereof.
  • As further represented in FIG. 1, a connector generally indicated as 40 is dimensioned and configured to be at least partially mounted on the outer surface 38′ of the connecting flange 38. When so positioned, the connecting flange 38 serves to interconnect the body 30 to correspondingly disposed interior portions, as at 42, of the housing 14. In more specific terms, at least one embodiment of the connector 40 may include a substantially annular configuration at least partially corresponding to the annular configuration of the connecting flange 38 and outer exposed surface 38′. Further, the connector 40 may be at least partially formed from an adhesive material or have adhesive characteristics sufficient to adhesively interconnect the mounting flange 38 and accordingly the remainder of the body 30 to interior surface portions or other corresponding portions 42 within the housing 14.
  • Therefore, it is emphasized that the locking device 10 may be operatively mounted and/or connected within the interior of the housing 14 and as such may be an original component of the dispenser assembly 12 as it is initially manufactured, produced and/or assembled. In contrast, the structural versatility of the locking device 10 enables it to be added to a dispenser assembly 12, of the type represented in FIG. 2, as an “add-on” component. In either application, the locking device 10 is structured to facilitate the original manufacture or the conversion of a dispenser assembly 12 to a “single-use” dispenser. In doing so, many of the disadvantages and problems recognized in the structural and operative features of known devices of this type are overcome. As set forth herein such problems include, but are not limited to, the monitoring or regulating of the individual dose of material being dispensed from the dispenser assembly 12.
  • Accordingly, the structural and operative features of the locking device 10 which enables the operation and use of a dispenser assembly 12 as a “single-use” dispenser includes the provision of a locking structure generally indicated as 46. More specifically, the locking structure 46 preferably comprises a locking structure 46 in the form of locking flange 48. The locking structure and locking flange 48 is connected exteriorly of the body 30 to the outer cylindrical wall 30′ preferably, but not necessarily, adjacent or contiguous to a corresponding end 32. In addition, the locking flange 48, due at least in part to the material from which it is formed or alternatively due to its connection to the body 30, is at least partially flexible and/or demonstrates flexible characteristics. Moreover, the maintenance of the plunger 20 in the non-operative and/or dispensed position renders the dispenser assembly 12 a single-use device. This is accomplished by the locking flange 48 frictionally engaging and possibly at least minimally penetrating corresponding interior surfaces as at 21′ as clearly represented in FIGS. 6 and 7.
  • Therefore, as the plunger 20 is pushed inwardly into the interior of the housing 14, the activating member 22 will operatively engage the dispensing portion 16 causing the dispensing of the intended material from the delivery portion or nozzle 18, as intended. However, the forced inward travel of the plunger 20 will also result in the interior surface portions 21 passing into sliding, frictional engagement with the locking flange 48 defining the locking structure 46. Therefore, as represented in FIGS. 6 and 7, at least the outer free end or periphery 48′ of the locking flange 48 will slidingly engage the correspondingly disposed interior surfaces 21 of the plunger 20 resulting in a frictional engagement therebetween. Further, when such frictional engagement occurs the locking flange 48 may be forced or “biased” inwardly towards the outer cylindrical wall 30′. Due to the flexible characteristics of the locking flange 48 as well as the material from which it is formed, the locking flange 48 will be normally biased outwardly into the orientation or position represented in FIG. 2, when the locking flange 48 is not engaged by the plunger 20, as at plunger portion or surface 21. However, once frictional engagement occurs between the interior surfaces 21 and the plunger 20 the locking flange 48, the locking flange 48 will be at least partially biased inwardly towards the outer cylindrical wall 30′. This biased, frictional engagement may result in at least minimal embedding, scraping, penetrating, etc. of the outer free periphery 48′ into the interior surfaces 21, as at 21′, of the plunger 20 as at least partially represented in FIGS. 6 and 7.
  • As a result the plunger 20 will be maintained into a movement restricting engagement with the locking flange 48 of the locking structure 46 and/or the outer free peripheral end 48′. The plunger 20 will thereby be prevented from being returned to the operative or ready position as represented in FIGS. 2 and 4. The provision of the locking device 10 and its interactive movement restricting engagement with the interior surfaces 21 of the plunger 20 will thereby render the dispenser assembly 12, with which the locking device 10 is used, as a “single-use” dispenser, as set forth above.
  • Further structural features of the locking device 10 include the open interior of the body 10 and the direct communication of the open ends 32 and 34 therewith. As a result, the locking device 10, including the body 30 can be said to be operatively mounted in at least partially surrounding relation to the dispensing portion 16 of the dispenser assembly 12 as clearly represented throughout the Figures. Further the opened distal end 32 of the body 30 allows passage of the activating member 22 of the plunger 20 into activating or operative engagement with the dispensing portion 16 of the dispenser assembly 12 as clearly represented in FIGS. 5 through 7. Therefore, the open interior of the body 30 of the locking device 10 can be said to be in receiving relation to the plunger 20 or at least the activating portion 22 thereof when the plunger 20 is forced into the dispensed position as clearly represented in FIG. 6. When the activating portion 22 of the plunger 20 is in the aforementioned dispensed position the body 30 and the outer cylindrical wall 30′ can also be said to be in at least partially surrounding relation with both the dispensing portion 16 as well as the activating portion 22 of the plunger 20.
  • Since many modifications, variations and changes in detail can be made to the described preferred embodiment of the invention, it is intended that all matters in the foregoing description and shown in the accompanying drawings be interpreted as illustrative and not in a limiting sense. Thus, the scope of the invention should be determined by the appended claims and their legal equivalents.
  • Now that the invention has been described,

Claims (23)

What is claimed is:
1. A dispenser assembly structured for a single-use application, said dispenser assembly comprising:
a housing including a dispensing portion disposed and structured to deliver material from said housing,
a plunger movably connected to said housing and disposable thereon between an operative position and inoperative position,
a locking device disposed within said housing and structured to facilitate passage of said plunger from said operative position into said inoperative position, and
said locking device including a locking structure disposed and configured for movement restricting engagement with said plunger when said plunger is in said inoperative position.
2. A dispenser assembly as recited in claim 1 wherein said movement restricting engagement comprises a frictional engagement of said locking structure with said plunger.
3. A dispenser assembly as recited in claim 2 wherein said movement restricting engagement further comprises a movable sliding engagement between said locking structure and said plunger.
4. A dispenser assembly as recited in claim 1 wherein said locking device is connected within said housing and includes an open interior, said open interior disposed in receiving relation to said plunger when in said inoperative position.
5. A dispenser assembly as recited in claim 4 wherein said locking structure is disposed exteriorly of said open interior in sliding, frictional engagement with said plunger.
6. A dispenser assembly as recited in claim 4 wherein said locking structure comprises a flange connected to an exterior of said locking device and extending outwardly therefrom, said flange at least partially formed of a flexible material, said movement restricting engagement comprises said flange disposed in biased engagement with said plunger.
7. A dispenser assembly as recited in claim 4 wherein said open interior is disposed in at least partially surrounding relation to said dispensing portion and said plunger when said plunger is in said inoperative position.
8. A dispenser assembly as recited in claim 1 wherein said locking device comprises a body including an open at least partially hollow interior disposed in receiving relation to said plunger when in said inoperative position.
9. A dispenser assembly as recited in claim 8 wherein said locking structure is connected to an exterior of said body and extends outwardly therefrom into said movement restricting engagement with said plunger when in said inoperative position.
10. A dispenser assembly as recited in claim 9 wherein said body comprises a substantially cylindrical outer wall configuration; said locking structure comprising a flange connected to an exterior of said outer wall and extending outwardly therefrom.
11. A dispenser assembly as recited in claim 10 wherein said flange is at least partially formed from a flexible material and comprises an at least partially annular configuration connected to and extending outwardly from an exterior of said outer wall and in at least partially surrounding relation thereto.
12. A dispenser assembly as recited in claim 8 further comprising a connector disposed in interconnecting relation between said body and interior of said housing.
13. A dispenser assembly as recited in claim 12 wherein said body comprises a head portion; said connector disposed in interconnecting relation between said head portion and an interior portion of said housing.
14. A dispenser assembly as recited in claim 13 wherein said connector is at least partially formed of an adhesive material disposed to adhesively secure said body to said housing.
15. A dispenser assembly as recited in claim 13 wherein said head portion is disposed transversely outward in at least partially surrounding relation to an open end of said body, said head portion including an outer exposed surface, said connector mounted on said exposed surface in attached engagement with an interior of said housing.
16. A locking device structured to maintain an activating plunger of a dispenser assembly in an inoperative position, said locking device comprising:
a body dimensioned and configured to be disposed with an interior of a housing of a dispenser assembly and in accessible relation to the plunger,
said body including a locking structure disposed thereon in movement restricting engagement with the plunger when the plunger is in an operative position,
said body comprising an open interior disposed in receiving relation to the plunger when disposed from an operative position to an inoperative position, and
said locking structure disposed on an exterior of said body in sliding, frictional engagement with the plunger when in the inoperative position.
17. A locking device as recited in claim 16 wherein said body comprises a substantially cylindrical outer wall configuration; said locking structure comprising a flange connected to an exterior of said outer wall and extending outwardly therefrom.
18. A locking device as recited in claim 17 wherein said flange is at least partially formed of a flexible material and comprises an at least partially annular configuration connected to and extending outwardly from an exterior of said outer wall and in at least partially surrounding relation thereto.
19. A locking device as recited in claim 18 wherein said flange is flexibly connected to said outer wall, said movement restricting engagement comprising said flange biased into said frictional, movement restricting engagement with the plunger.
20. A locking device as recited in claim 16 further comprising a connector disposed in interconnecting relation between said body and an interior of the dispenser assembly.
21. A locking device as recited in claim 20 wherein said body comprises a head portion; said connector disposed in interconnecting relation between said head portion and interior of said dispenser assembly.
22. A locking device as recited in claim 21 wherein said connector is at least partially formed of an adhesive material disposed to adhesively secure said body to the interior of the dispenser assembly.
23. A locking device as recited in claim 21 wherein said head portion is disposed in at least partially surrounding relation to said body and includes an outer exposed surface, said connector mounted on said exposed surface in attached engagement with an interior of said housing.
US13/962,007 2013-08-08 2013-08-08 Single use enhancement for dispenser assembly Abandoned US20150041496A1 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US13/962,007 US20150041496A1 (en) 2013-08-08 2013-08-08 Single use enhancement for dispenser assembly
PCT/EP2014/066925 WO2015018869A1 (en) 2013-08-08 2014-08-06 Single use enhancement for dispenser assembly

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US13/962,007 US20150041496A1 (en) 2013-08-08 2013-08-08 Single use enhancement for dispenser assembly

Publications (1)

Publication Number Publication Date
US20150041496A1 true US20150041496A1 (en) 2015-02-12

Family

ID=51399615

Family Applications (1)

Application Number Title Priority Date Filing Date
US13/962,007 Abandoned US20150041496A1 (en) 2013-08-08 2013-08-08 Single use enhancement for dispenser assembly

Country Status (2)

Country Link
US (1) US20150041496A1 (en)
WO (1) WO2015018869A1 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9474869B2 (en) 2011-02-28 2016-10-25 Kaleo, Inc. Medicament delivery device for administration of opioid antagonists including formulations for naloxone
US9517307B2 (en) 2014-07-18 2016-12-13 Kaleo, Inc. Devices and methods for delivering opioid antagonists including formulations for naloxone
US9814838B2 (en) 2011-01-26 2017-11-14 Kaleo, Inc. Medicament delivery device for administration of opioid antagonists including formulations for naloxone
US20190381236A1 (en) * 2018-06-18 2019-12-19 Omar-Samir M. Badr Autoinjector carrier

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050279776A1 (en) * 2003-12-12 2005-12-22 Airlessystems Fluid dispenser
US20060097012A1 (en) * 2003-04-23 2006-05-11 Eric Rossignol Single-dose cosmetic sample dispenser
US7497359B2 (en) * 2002-02-07 2009-03-03 3M Innovative Properties Company Dosing device
US7726519B2 (en) * 2002-11-29 2010-06-01 Valois S.A.S. Fluid dispenser device

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2649323B1 (en) * 1989-07-04 1995-06-30 Valois DEVICE FOR SPRAYING AND SPRAYING A DOSE OF A DIVIDABLE PRODUCT
US5215079A (en) * 1992-05-19 1993-06-01 Armstrong Pharmaceuticals, Inc. Single dose metered dose inhaler for delivery of vaccines and other drugs
US5733261A (en) * 1996-03-08 1998-03-31 Obong; Ekoi Edet Single use locking syringe
GB2367756B (en) * 2000-10-12 2003-01-08 Bespak Plc Dispensing apparatus
MX2008002090A (en) * 2005-08-24 2008-04-19 Boehringer Ingelheim Int Atomiser comprising a counter and an end of operation lock.
WO2008103175A1 (en) * 2007-02-22 2008-08-28 M2 Group Holdings, Inc. Portable infusion pump with flexible piston rod
US20100095957A1 (en) * 2007-03-02 2010-04-22 Corbco, Inc. Manually operated monodose nasal sprayer device
DK2526989T3 (en) * 2011-05-23 2020-04-06 Boehringer Ingelheim Int SYSTEM INCLUDING A SPRAYER

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7497359B2 (en) * 2002-02-07 2009-03-03 3M Innovative Properties Company Dosing device
US7726519B2 (en) * 2002-11-29 2010-06-01 Valois S.A.S. Fluid dispenser device
US20060097012A1 (en) * 2003-04-23 2006-05-11 Eric Rossignol Single-dose cosmetic sample dispenser
US20050279776A1 (en) * 2003-12-12 2005-12-22 Airlessystems Fluid dispenser

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9814838B2 (en) 2011-01-26 2017-11-14 Kaleo, Inc. Medicament delivery device for administration of opioid antagonists including formulations for naloxone
US10322239B2 (en) 2011-01-26 2019-06-18 Kaleo, Inc. Medicament delivery device for administration of opioid antagonists including formulations for naloxone
US9474869B2 (en) 2011-02-28 2016-10-25 Kaleo, Inc. Medicament delivery device for administration of opioid antagonists including formulations for naloxone
US10143792B2 (en) 2011-02-28 2018-12-04 Kaleo, Inc. Medicament delivery device for administration of opioid antagonists including formulations for naloxone
US9517307B2 (en) 2014-07-18 2016-12-13 Kaleo, Inc. Devices and methods for delivering opioid antagonists including formulations for naloxone
US10220158B2 (en) 2014-07-18 2019-03-05 Kaleo, Inc. Devices and methods for delivering opioid antagonists including formulations for naloxone
US20190381236A1 (en) * 2018-06-18 2019-12-19 Omar-Samir M. Badr Autoinjector carrier

Also Published As

Publication number Publication date
WO2015018869A1 (en) 2015-02-12

Similar Documents

Publication Publication Date Title
ES2345694T3 (en) DEVICE FOR MANAGING MEDICANTS.
CN110559522B (en) Safety syringe
JP6002288B2 (en) Injection pen with dial back and final dose control
KR101870065B1 (en) Medicament delivery device
US5601077A (en) Nasal syringe sprayer with removable dose limiting structure
US6796967B2 (en) Injection needle assembly
RU2514114C2 (en) Device for introduction of medication and method of work with device for introduction of medication
JP5663091B2 (en) Drug delivery device
TWI576128B (en) Medicament delivery device
US9238106B2 (en) Dose setting mechanism for priming a drug delivery device
TWI577409B (en) Medicament delivery device
JP6047244B2 (en) Drug delivery device
US20150041496A1 (en) Single use enhancement for dispenser assembly
US20100228200A1 (en) Dosage delivery device
US20150352298A1 (en) Medicament Delivery Device
MXPA06013893A (en) Releasable coupling and injection device.
JP2016515434A (en) Drug delivery device
CN107427643B (en) Drug delivery device
TWI579012B (en) Medicament delivery device
JP2006204910A (en) Injection device for administering liquid medication
US7951120B2 (en) Method for manufacturing a syringe
WO2018051371A2 (en) Powder dispenser
JP2013509929A (en) Fluid dosing device
US10245387B2 (en) Medicament delivery device
EP3599031A1 (en) Discharger, container, dispensing part, activation part and method of assembling and using a discharger

Legal Events

Date Code Title Description
AS Assignment

Owner name: APTAR FRANCE SAS, FRANCE

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:KIM, SUNGMOON;KIM, BONGGEUN;REEL/FRAME:032025/0149

Effective date: 20140116

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION