US3110308A - Parenteral fluid administration equiment - Google Patents

Parenteral fluid administration equiment Download PDF

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US3110308A
US3110308A US63923A US6392360A US3110308A US 3110308 A US3110308 A US 3110308A US 63923 A US63923 A US 63923A US 6392360 A US6392360 A US 6392360A US 3110308 A US3110308 A US 3110308A
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tubing
cannula
container
blood
membrane
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Jr David Bellamy
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Baxter International Inc
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Baxter Laboratories Inc
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61JCONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
    • A61J1/00Containers specially adapted for medical or pharmaceutical purposes
    • A61J1/05Containers specially adapted for medical or pharmaceutical purposes for collecting, storing or administering blood, plasma or medical fluids ; Infusion or perfusion containers
    • A61J1/10Bag-type containers

Definitions

  • the present invention relates to parenteral fluid administration equipment. More particularly, it relates to an externally manipulable, internally located valve system especially useful in the parenteral fluid administration field.
  • Resilient tubing such as plastic and rubber tubing finds wide usage in the parenteral fluid administration field.
  • One such use is in the recently introduced multicontainer blood collection and administration system, in which resilient tubing is used both as a conduit for the blood from the patient to a first blood collection chamber and as a conduit for blood from the first container to other containers or anti-coagulant from secondary to primary container.
  • the multi-chambered blood systems among other functions permit the conservation of whole blood, for example, by allowing, if desired, the division of a single pint of blood into pediatric quantities to be used individually or by allowing, if desired, the holding of the whole blood unadulterated by long term anticoagulants in the first container for the maximum period of time and then transferring the blood to a second chamber containing anticoagulants to extend the storage period.
  • the closed multi-container blood systems depend largely for their elfectiveness upon the use of a positive off type valve or clamp which prevents the flow of the blood through the tubing from the first to the second container.
  • valves or clamps may be used to more or less positively shut off the flow of fluids such as blood through the resilient tubing, the use of such valves is always accompanied by the risk of dislodgment, etc., and damage to the tubing itself.
  • FIGURE 1 is an assembly view of a multi-container blood system showing the novel valve system of the present invention in pre-use condition.
  • FIGURE 2 is a sectional view in larger scale of the novel valve system.
  • FIGURE 1 a multi-container blood collecting and storing means having a flexible donor tube 11.
  • the tube 11 provides at its outer end a phlebotomy needle 12 which is specially sharpened to minimize tissue trauma.
  • the needle 12 is equipped with a protective sheath or cover 13 to protect against dulling and contamination.
  • the container is preferably formed by juxtaposing sheets of thermoplastic material and heat sealing them along the edges.
  • the donor tube 11 is sealed through the end 14 of the bag as is the port assembly and closure 15.
  • the multi-container blood system further comprises as a transfer or storage means, a second flexible container 29 which is similar in form and construction to container it) and which is integrally joined thereto by connector tubing 21 of suitable length.
  • the tube 21 is provided with an internal cannula 22 of steel, plastic or the like which is proportioned to fit in and move easily within the connecting tube.
  • the tube 21 is removably closed adjacent container 10 by a transverse membrane 23 which is removed by external manipulation of the cannula 22 which is seen as having a sharpened beveled or pointed end 24 for this purpose.
  • the cannula 22 is preferably coated or otherwise treated to present a hemorepellant surface. It may, if desired, also be provided with a flange or rounded butt end opposite its pointed end to make it more readily manipulable without damaging the tubing.
  • FIGURE 2 the pointed cannula and puncturable transverse membrane are shown prior to use, enlarged and in greater detail.
  • the protective sheath is removed -from the phlebotomy needle 12 and the vein of the donor punctured. The donation is then collected into the first container and collection ceased. If only a small portion of the blood is to be given initially or if after maxi-mum storage without an anticoagulant or with a short term anticoagulant it is desired to add an anticoagulant to the blood, the cannula is manipulated as for example, by compressing the tubing adjacent the blunt end of the cannula and collapsing the tubing thus forcing the cannula into puncturing relationship with the diaphragm, at which time the blood may be allowed to flow from the first to the second container.
  • the second container may, of course, be of different size and/or contain an anticoagulant if so desired.
  • novel inline cannula-membrane valve system described in detail above in connection with parenteral fluid administration equipment may of course be advantageously used in other fields to overcome the problem of retaining completely separate two or more solutions and yet preserving the possibility of combining them simply and easily if so desired.
  • a donor tube having needle means at one end and communicating with a flexible, collapsible, hemo-repellant blood container at the other end, a length of resilient tubing connecting said container to a second flexible, collapsible container to form a unitary system, a removable, transverse membrane positively closing said connecting tubing to the flow of fluid between said containers and a free moving membrane-removing, hollow cannula located wholly within said tubing, the cannula being completely unattached to said tubing and any part of said system, said cannula being proportioned :to readily fit in and move within said tubing so that the cannula can be externally manipulated to remove said membrane without opening said tubing, said cannula being further manipulatable substantially out of said tubing into one of said containers.
  • an improved removable closing means for controlling flow between said containers which means provides initially for a complete and positive obstruction to flow through said tubing and between said containers, and upon removal for a substantially and unobstructed flow through said tubing, said means comprising a removable transverse membrane barrier positively closing said connecting tubing to flow and a free moving membrane piercing cannula proportioned to fit in and freely move within said tubing, said cannula being completely unattached to said tubing and any part of said system so that it can be manipulated from outside said tubing to substantially remove said membrane and then may be further manipulated substantially out of said tubing into one of said containers so that flow through said tubing is substantially unobstructed and non-turbulent.
  • a multi-container system for the conditioning and handling of blood comprised of at least two flexible, collapsible, hemo-repellant sterile blood containers, each having a blood inlet and an outlet, a length of resilient tubing connecting said flexible containers, a transverse membrane positively closing said tubing to flow and preventing flow between the containers joined by said tubing and a free moving membrane removing member located wholly within said tubing, said membrane removing member being completely unattached to said tubing and being so proportioned as to fit in and move freely Within said tubing so that it can be externally manipulated without opening said tubing to remove said membrane and may further be manipulated substantially out of said tubing into one of said containers so that flow through said tubing and between said containers is substantially unobstructed and non-turbulent.
  • a multi-container closed system for the storage and handling of blood which system comprises at least two flexible, collapsible hemo-repellant containers joined together by a length of resilient connecting tubing, at
  • said containers containing a substance which it is desired to isolate in said container, an improved means for preventing flow through said tubing and among said containers, and isolating said substance in said container, the improved means of preventing flow providing for positive closing of said tubing to flow, and comprising a removable transverse membrane completely closing said connecting tubing to fluid flow and a free moving, membrane piercing hollow cannula located wholly within said tubing, the cannula being completely unattached to said tubing and any part of said system, said cannula being proportioned to readily fit in and freely move within said tubing so that the cannula can be externally manipulated from without said system to substantially remove said membrane as an obstacle to fluid flow Without opening said closed system and thus allow for the introduction into another container of the system of the previously isolated substance.

Description

Nov. 12, 1963 D. BELLAMY, JR 3,110,30g
PARENTERAL FLUID ADMINISTRATION EQUIPMENT Filed Oct. 20, 1960 INVEN TOR.
DAVID BELLAMY JR.
BY M @W ATTORNEY United States Patent Ofltice 3,1 19,368 Patented Nov; 12, 1963 3,110,308 PARENTERAL FLUID ADMINISTRATIUN EQUEMENT David Bellamy, Jan, Framingham, Mass, assignor to Baxter Laboratories, Inc, Morton Grove, 11]., a corporation of Delaware Filed Oct. 20, 1960, Ser. No. 63,923 4 Claims. (Cl. 128-214) The present invention relates to parenteral fluid administration equipment. More particularly, it relates to an externally manipulable, internally located valve system especially useful in the parenteral fluid administration field.
Resilient tubing, such as plastic and rubber tubing finds wide usage in the parenteral fluid administration field. One such use is in the recently introduced multicontainer blood collection and administration system, in which resilient tubing is used both as a conduit for the blood from the patient to a first blood collection chamber and as a conduit for blood from the first container to other containers or anti-coagulant from secondary to primary container. The multi-chambered blood systems among other functions permit the conservation of whole blood, for example, by allowing, if desired, the division of a single pint of blood into pediatric quantities to be used individually or by allowing, if desired, the holding of the whole blood unadulterated by long term anticoagulants in the first container for the maximum period of time and then transferring the blood to a second chamber containing anticoagulants to extend the storage period. The closed multi-container blood systems depend largely for their elfectiveness upon the use of a positive off type valve or clamp which prevents the flow of the blood through the tubing from the first to the second container.
While many externally located valves or clamps may be used to more or less positively shut off the flow of fluids such as blood through the resilient tubing, the use of such valves is always accompanied by the risk of dislodgment, etc., and damage to the tubing itself.
It is therefore an object of the present invention to disclose a novel externally manipulable, internally located valve system for use in resilient tubing which is not accompanied by the aforesaid disadvantages.
It is further an object to disclose a closed multi-container blood system embodying the novel valve system of the present invention.
These and still other objects will become more apparent from the following description and drawing in which like reference characters denote like parts throughout the several views.
FIGURE 1 is an assembly view of a multi-container blood system showing the novel valve system of the present invention in pre-use condition.
FIGURE 2 is a sectional view in larger scale of the novel valve system.
In the exemplary form of the drawing, FIGURE 1, is shown a multi-container blood collecting and storing means having a flexible donor tube 11. The tube 11 provides at its outer end a phlebotomy needle 12 which is specially sharpened to minimize tissue trauma. The needle 12 is equipped with a protective sheath or cover 13 to protect against dulling and contamination.
The container is preferably formed by juxtaposing sheets of thermoplastic material and heat sealing them along the edges. The donor tube 11 is sealed through the end 14 of the bag as is the port assembly and closure 15.
The multi-container blood system further comprises as a transfer or storage means, a second flexible container 29 which is similar in form and construction to container it) and which is integrally joined thereto by connector tubing 21 of suitable length. In accordance with the present invention the tube 21 is provided with an internal cannula 22 of steel, plastic or the like which is proportioned to fit in and move easily within the connecting tube. The tube 21 is removably closed adjacent container 10 by a transverse membrane 23 which is removed by external manipulation of the cannula 22 which is seen as having a sharpened beveled or pointed end 24 for this purpose.
The cannula 22 is preferably coated or otherwise treated to present a hemorepellant surface. It may, if desired, also be provided with a flange or rounded butt end opposite its pointed end to make it more readily manipulable without damaging the tubing.
In FIGURE 2 the pointed cannula and puncturable transverse membrane are shown prior to use, enlarged and in greater detail.
In the obtaining and storage of the blood ultilizing the above described apparatus, the protective sheath is removed -from the phlebotomy needle 12 and the vein of the donor punctured. The donation is then collected into the first container and collection ceased. If only a small portion of the blood is to be given initially or if after maxi-mum storage without an anticoagulant or with a short term anticoagulant it is desired to add an anticoagulant to the blood, the cannula is manipulated as for example, by compressing the tubing adjacent the blunt end of the cannula and collapsing the tubing thus forcing the cannula into puncturing relationship with the diaphragm, at which time the blood may be allowed to flow from the first to the second container. The second container may, of course, be of different size and/or contain an anticoagulant if so desired.
The novel inline cannula-membrane valve system described in detail above in connection with parenteral fluid administration equipment may of course be advantageously used in other fields to overcome the problem of retaining completely separate two or more solutions and yet preserving the possibility of combining them simply and easily if so desired.
While an embodiment has been described in which a single tube with an integral transverse membrane and a steel cannula are employed, it is readily apparent that a membrane present at the junction of two lengths of tubing or a rigid or semi-rigid plastic cannula 'or the like may also be used without departing from the spirit or scope of the present invention.
The embodiments of the invention in which an exclusive property or privilege is claimed are as follows:
1. In parenteral fluid administration equipment a donor tube having needle means at one end and communicating with a flexible, collapsible, hemo-repellant blood container at the other end, a length of resilient tubing connecting said container to a second flexible, collapsible container to form a unitary system, a removable, transverse membrane positively closing said connecting tubing to the flow of fluid between said containers and a free moving membrane-removing, hollow cannula located wholly within said tubing, the cannula being completely unattached to said tubing and any part of said system, said cannula being proportioned :to readily fit in and move within said tubing so that the cannula can be externally manipulated to remove said membrane without opening said tubing, said cannula being further manipulatable substantially out of said tubing into one of said containers.
2. In a multi-container closed system for handling blood comprising at least two flexible, collapsible, hemorepellant sterile blood containers joined together by lengths of resilient connecting tubing, an improved removable closing means for controlling flow between said containers which means provides initially for a complete and positive obstruction to flow through said tubing and between said containers, and upon removal for a substantially and unobstructed flow through said tubing, said means comprising a removable transverse membrane barrier positively closing said connecting tubing to flow and a free moving membrane piercing cannula proportioned to fit in and freely move within said tubing, said cannula being completely unattached to said tubing and any part of said system so that it can be manipulated from outside said tubing to substantially remove said membrane and then may be further manipulated substantially out of said tubing into one of said containers so that flow through said tubing is substantially unobstructed and non-turbulent.
3. :In a multi-container system for the conditioning and handling of blood comprised of at least two flexible, collapsible, hemo-repellant sterile blood containers, each having a blood inlet and an outlet, a length of resilient tubing connecting said flexible containers, a transverse membrane positively closing said tubing to flow and preventing flow between the containers joined by said tubing and a free moving membrane removing member located wholly within said tubing, said membrane removing member being completely unattached to said tubing and being so proportioned as to fit in and move freely Within said tubing so that it can be externally manipulated without opening said tubing to remove said membrane and may further be manipulated substantially out of said tubing into one of said containers so that flow through said tubing and between said containers is substantially unobstructed and non-turbulent.
4. In a multi-container closed system for the storage and handling of blood, which system comprises at least two flexible, collapsible hemo-repellant containers joined together by a length of resilient connecting tubing, at
least one of said containers containing a substance which it is desired to isolate in said container, an improved means for preventing flow through said tubing and among said containers, and isolating said substance in said container, the improved means of preventing flow providing for positive closing of said tubing to flow, and comprising a removable transverse membrane completely closing said connecting tubing to fluid flow and a free moving, membrane piercing hollow cannula located wholly within said tubing, the cannula being completely unattached to said tubing and any part of said system, said cannula being proportioned to readily fit in and freely move within said tubing so that the cannula can be externally manipulated from without said system to substantially remove said membrane as an obstacle to fluid flow Without opening said closed system and thus allow for the introduction into another container of the system of the previously isolated substance.
tion of Blood Components, from Bibieotheca Haematologica (Basel), vol. 7, Jan. 20, 1958 (copy in Div.
Earl et al.: A Practical Method for the Aseptic Preparation of Human Platelet Concentrates With-out Loss of Other Blood Elements/f from New England Journal of Medicine, 254:l1321133, June 14, 1956.

Claims (1)

1. IN PARENTERAL FLUID ADMINISTRATION EQUIPMENT A DONOR TUBE HAVING NEEDLE MEANS AT ONE END AND COMMUNICATING WITH A FLEXIBLE, COLLAPSIBLE, HEMO-REPELLANT BLOOD CONTAINER AT THE OTHER END, A LENGTH OF RESILIENT TUBING CONNECTING SAID CONTAINER TO A SECOND FLEXIBLE, COLLAPSIBLE CONTAINER TO FORM A UNITARY SYSTEM, A REMOVABLE, TRANSVERSE MEMBRANE POSITIVELY CLOSING SAID CONNECTING TUBING TO THE FLOW OF FLUID BETWEEN SAID CONTAINERS AND A FREE MOVING MEMBRANE-REMOVING, HOLLOW CANNULA LOCATED WHOLLY WITHIN SAID TUBING, THE CANNULA BEING COMPLETELY UNATTACHED TO SAID TUBING AND ANY PART OF SAID SYSTEM, SAID CANNULA BEING PROPORTIONED TO READILY FIT IN AND MOVE WITHIN SAID TUBING SO THAT THE CANNULA CAN BE EXTERNALLY MANIPULATED TO REMOVE SAID MEMBRANE WITHOUT OPENING SAID TUBING, SAID CANNULA BEING FURTHER MANIPULATABLE SUBSTANTIALLY OUT OF SAID TUBING INTO ONE OF SAID CONTAINERS.
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Cited By (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3276589A (en) * 1961-12-18 1966-10-04 Jankay Lester Apparatus for maintenance and treatment of blood in vitro
US3648693A (en) * 1969-05-28 1972-03-14 Jintan Terumo Co Bag apparatus for transfusion of blood or fluid involving heat shrinkable tube means
US3677248A (en) * 1970-08-27 1972-07-18 American Hospital Supply Corp Surgical irrigation apparatus and method of using same
US3788374A (en) * 1972-01-26 1974-01-29 Jintan Terumo Co Parenteral solution bag
US3870042A (en) * 1971-10-13 1975-03-11 Lab Medicoplast Apparatus for separating and injecting blood component
DE2439392A1 (en) * 1973-10-23 1975-04-24 Sorenson Research Co DEVICE AND METHOD FOR ASEPTIC COLLECTION OF FLUIDS BY VACUUM PRESSURE
US3986506A (en) * 1974-09-03 1976-10-19 Baxter Travenol Laboratories, Inc. Apparatus for separation of cryoprecipitate from blood plasma and method
US4007738A (en) * 1974-07-31 1977-02-15 Terumo Corporation Mechanism for allowing blood bags to communicate with each other
US4056116A (en) * 1976-09-08 1977-11-01 Baxter Travenol Laboratories, Inc. Valve for interconnecting sterile containers and the like
US4183434A (en) * 1977-09-02 1980-01-15 Pharmachem Corporation Peelable seal
US4195632A (en) * 1978-05-03 1980-04-01 Cutter Laboratories, Inc. Fluid flow valve
US4198972A (en) * 1978-04-17 1980-04-22 Pharmachem Corporation Blood and blood component storage bags
FR2450752A1 (en) * 1979-03-05 1980-10-03 Baxter Travenol Lab SEPARABLE SEALING CLOSURE FOR FLEXIBLE CONTAINER; BLOOD BAG COMPRISING SUCH A BODY AND METHOD FOR CLOSING A FLEXIBLE CONTAINER BY MEANS OF SUCH A BODY
FR2453652A1 (en) * 1979-04-09 1980-11-07 Baxter Travenol Lab IMPROVEMENT IN FLAT-CONTAINABLE CONTAINERS FOR MEDICAL USE SOLUTIONS
US4232721A (en) * 1979-04-09 1980-11-11 Baxter Travenol Laboratories, Inc. Collapsible solution container having rectangular shoulder
US4234026A (en) * 1979-03-05 1980-11-18 Baxter Travenol Laboratories, Inc. Seal for flexible container
US4305443A (en) * 1979-03-05 1981-12-15 Baxter Travenol Laboratories, Inc. Seal for flexible container having flexible, generally conical portions
US4320789A (en) * 1979-04-09 1982-03-23 Baxter Travenol Laboratories, Inc. Collapsible solution container
WO1983001569A1 (en) * 1981-11-09 1983-05-11 Baxter Travenol Lab Multiple chamber solution container including positive test for homogenous mixture
DE3238836A1 (en) * 1982-03-12 1983-09-22 Terumo K.K., Tokyo MEDICAL DEVICE AND METHOD FOR THEIR PRODUCTION
DE3238834A1 (en) * 1982-03-12 1983-09-22 Terumo K.K., Tokyo CANNULA UNIT AND MEDICAL BAG WITH IT
US4465488A (en) * 1981-03-23 1984-08-14 Baxter Travenol Laboratories, Inc. Collapsible multi-chamber medical fluid container
US4915683A (en) * 1986-11-21 1990-04-10 The Medical College Of Wisconsin, Inc. Antiviral method, agents and apparatus
US4994039A (en) * 1985-11-15 1991-02-19 Mattson Philip D Apparatus and method for patients from a single donor or a restricted group of donors
US5039483A (en) * 1987-03-10 1991-08-13 The Medical College Of Wisconsin, Inc. Antiprotozoan method
US5114004A (en) * 1990-02-14 1992-05-19 Material Engineering Technology Laboratory Inc. Filled and sealed, self-contained mixing container
US5167656A (en) * 1991-01-22 1992-12-01 Baxter International Inc. Blood container having lay-flat sample reservoir
US5304113A (en) * 1986-11-21 1994-04-19 The Mcw Research Foundation, Inc. Method of eradicating infectious biological contaminants
US20030146170A1 (en) * 2002-02-01 2003-08-07 Frank Corbin Whole blood collection and processing method
US6764482B2 (en) 1996-05-03 2004-07-20 Baxter International Inc. Dual-filled twin bag, a package and a method for forming a package for administering a solution
US20040233779A1 (en) * 2003-05-19 2004-11-25 Jean-Pascal Zambaux Flexible mixing bag for mixing solids, liquids and gases
DE102004015031A1 (en) * 2004-03-27 2005-10-20 Drk Blutspendedienst West Ggbm Transitional closure for blood bag systems
JP2010188197A (en) * 2010-06-09 2010-09-02 Jms Co Ltd Blood component dispenser

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1082035A (en) * 1953-05-28 1954-12-24 Apparatus for collecting, storing and distributing human blood
US2702034A (en) * 1950-07-20 1955-02-15 Fenwal Inc Apparatus for collecting, storing, and dispensing whole blood

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2702034A (en) * 1950-07-20 1955-02-15 Fenwal Inc Apparatus for collecting, storing, and dispensing whole blood
FR1082035A (en) * 1953-05-28 1954-12-24 Apparatus for collecting, storing and distributing human blood

Cited By (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3276589A (en) * 1961-12-18 1966-10-04 Jankay Lester Apparatus for maintenance and treatment of blood in vitro
US3648693A (en) * 1969-05-28 1972-03-14 Jintan Terumo Co Bag apparatus for transfusion of blood or fluid involving heat shrinkable tube means
US3677248A (en) * 1970-08-27 1972-07-18 American Hospital Supply Corp Surgical irrigation apparatus and method of using same
US3870042A (en) * 1971-10-13 1975-03-11 Lab Medicoplast Apparatus for separating and injecting blood component
US3788374A (en) * 1972-01-26 1974-01-29 Jintan Terumo Co Parenteral solution bag
DE2439392A1 (en) * 1973-10-23 1975-04-24 Sorenson Research Co DEVICE AND METHOD FOR ASEPTIC COLLECTION OF FLUIDS BY VACUUM PRESSURE
US4007738A (en) * 1974-07-31 1977-02-15 Terumo Corporation Mechanism for allowing blood bags to communicate with each other
US3986506A (en) * 1974-09-03 1976-10-19 Baxter Travenol Laboratories, Inc. Apparatus for separation of cryoprecipitate from blood plasma and method
US4056116A (en) * 1976-09-08 1977-11-01 Baxter Travenol Laboratories, Inc. Valve for interconnecting sterile containers and the like
US4183434A (en) * 1977-09-02 1980-01-15 Pharmachem Corporation Peelable seal
US4198972A (en) * 1978-04-17 1980-04-22 Pharmachem Corporation Blood and blood component storage bags
US4195632A (en) * 1978-05-03 1980-04-01 Cutter Laboratories, Inc. Fluid flow valve
FR2450752A1 (en) * 1979-03-05 1980-10-03 Baxter Travenol Lab SEPARABLE SEALING CLOSURE FOR FLEXIBLE CONTAINER; BLOOD BAG COMPRISING SUCH A BODY AND METHOD FOR CLOSING A FLEXIBLE CONTAINER BY MEANS OF SUCH A BODY
US4234026A (en) * 1979-03-05 1980-11-18 Baxter Travenol Laboratories, Inc. Seal for flexible container
US4305443A (en) * 1979-03-05 1981-12-15 Baxter Travenol Laboratories, Inc. Seal for flexible container having flexible, generally conical portions
FR2453652A1 (en) * 1979-04-09 1980-11-07 Baxter Travenol Lab IMPROVEMENT IN FLAT-CONTAINABLE CONTAINERS FOR MEDICAL USE SOLUTIONS
US4232721A (en) * 1979-04-09 1980-11-11 Baxter Travenol Laboratories, Inc. Collapsible solution container having rectangular shoulder
US4320789A (en) * 1979-04-09 1982-03-23 Baxter Travenol Laboratories, Inc. Collapsible solution container
US4465488A (en) * 1981-03-23 1984-08-14 Baxter Travenol Laboratories, Inc. Collapsible multi-chamber medical fluid container
WO1983001569A1 (en) * 1981-11-09 1983-05-11 Baxter Travenol Lab Multiple chamber solution container including positive test for homogenous mixture
US4396383A (en) * 1981-11-09 1983-08-02 Baxter Travenol Laboratories, Inc. Multiple chamber solution container including positive test for homogenous mixture
DE3238834A1 (en) * 1982-03-12 1983-09-22 Terumo K.K., Tokyo CANNULA UNIT AND MEDICAL BAG WITH IT
DE3249823C2 (en) * 1982-03-12 1988-06-01 Terumo Kabushiki Kaisha Trading As Terumo Corp., Tokio/Tokyo, Jp
DE3238836A1 (en) * 1982-03-12 1983-09-22 Terumo K.K., Tokyo MEDICAL DEVICE AND METHOD FOR THEIR PRODUCTION
US4994039A (en) * 1985-11-15 1991-02-19 Mattson Philip D Apparatus and method for patients from a single donor or a restricted group of donors
US5304113A (en) * 1986-11-21 1994-04-19 The Mcw Research Foundation, Inc. Method of eradicating infectious biological contaminants
US4915683A (en) * 1986-11-21 1990-04-10 The Medical College Of Wisconsin, Inc. Antiviral method, agents and apparatus
US5039483A (en) * 1987-03-10 1991-08-13 The Medical College Of Wisconsin, Inc. Antiprotozoan method
US5114004A (en) * 1990-02-14 1992-05-19 Material Engineering Technology Laboratory Inc. Filled and sealed, self-contained mixing container
US5167656A (en) * 1991-01-22 1992-12-01 Baxter International Inc. Blood container having lay-flat sample reservoir
US6764482B2 (en) 1996-05-03 2004-07-20 Baxter International Inc. Dual-filled twin bag, a package and a method for forming a package for administering a solution
US20030146170A1 (en) * 2002-02-01 2003-08-07 Frank Corbin Whole blood collection and processing method
US20050274673A1 (en) * 2002-02-01 2005-12-15 Gambro, Inc Whole blood collection and processing method
US6994790B2 (en) 2002-02-01 2006-02-07 Gambro, Inc. Whole blood collection and processing method
US20040233779A1 (en) * 2003-05-19 2004-11-25 Jean-Pascal Zambaux Flexible mixing bag for mixing solids, liquids and gases
US7083323B2 (en) * 2003-05-19 2006-08-01 Advanced Technology Materials, Inc. Flexible mixing bag for mixing solids, liquids and gases
DE102004015031A1 (en) * 2004-03-27 2005-10-20 Drk Blutspendedienst West Ggbm Transitional closure for blood bag systems
JP2010188197A (en) * 2010-06-09 2010-09-02 Jms Co Ltd Blood component dispenser

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