EP0395758A1 - Behälter für getrennte lagerung - Google Patents
Behälter für getrennte lagerung Download PDFInfo
- Publication number
- EP0395758A1 EP0395758A1 EP88908369A EP88908369A EP0395758A1 EP 0395758 A1 EP0395758 A1 EP 0395758A1 EP 88908369 A EP88908369 A EP 88908369A EP 88908369 A EP88908369 A EP 88908369A EP 0395758 A1 EP0395758 A1 EP 0395758A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- piercing
- storage container
- separate storage
- chamber
- container according
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000003814 drug Substances 0.000 claims abstract description 40
- 238000004891 communication Methods 0.000 claims abstract description 23
- 239000004033 plastic Substances 0.000 claims abstract description 13
- 239000002904 solvent Substances 0.000 claims abstract description 10
- 239000000126 substance Substances 0.000 claims description 8
- 229920003002 synthetic resin Polymers 0.000 claims description 5
- 239000000057 synthetic resin Substances 0.000 claims description 5
- 229920005992 thermoplastic resin Polymers 0.000 claims description 4
- 238000000071 blow moulding Methods 0.000 claims description 3
- 239000007769 metal material Substances 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- 230000002093 peripheral effect Effects 0.000 claims description 3
- 238000000465 moulding Methods 0.000 claims description 2
- 229940079593 drug Drugs 0.000 abstract description 6
- 238000004090 dissolution Methods 0.000 abstract description 2
- 238000000926 separation method Methods 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 27
- YRMCBQLZVBXOSJ-PCFSSPOYSA-N (e)-3-[(6r,6as)-4-hydroxy-6-methoxy-3-methyl-11-oxo-5,6,6a,7-tetrahydropyrrolo[2,1-c][1,4]benzodiazepin-8-yl]prop-2-enamide Chemical compound CO[C@H]1NC2=C(O)C(C)=CC=C2C(=O)N2C=C(\C=C\C(N)=O)C[C@@H]12 YRMCBQLZVBXOSJ-PCFSSPOYSA-N 0.000 description 7
- 238000001990 intravenous administration Methods 0.000 description 6
- 238000010276 construction Methods 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Chemical compound OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 2
- 239000003242 anti bacterial agent Substances 0.000 description 2
- 230000003115 biocidal effect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000002504 physiological saline solution Substances 0.000 description 2
- -1 polypropylene Polymers 0.000 description 2
- 210000003462 vein Anatomy 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000010253 intravenous injection Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
Images
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61J—CONTAINERS 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
- A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
- A61J1/14—Details; Accessories therefor
- A61J1/20—Arrangements for transferring or mixing fluids, e.g. from vial to syringe
- A61J1/2093—Containers having several compartments for products to be mixed
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS 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
- B65D81/00—Containers, packaging elements, or packages, for contents presenting particular transport or storage problems, or adapted to be used for non-packaging purposes after removal of contents
- B65D81/32—Containers, packaging elements, or packages, for contents presenting particular transport or storage problems, or adapted to be used for non-packaging purposes after removal of contents for packaging two or more different materials which must be maintained separate prior to use in admixture
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61J—CONTAINERS 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
- A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
- A61J1/05—Containers specially adapted for medical or pharmaceutical purposes for collecting, storing or administering blood, plasma or medical fluids ; Infusion or perfusion containers
- A61J1/10—Bag-type containers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61J—CONTAINERS 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
- A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
- A61J1/14—Details; Accessories therefor
- A61J1/20—Arrangements for transferring or mixing fluids, e.g. from vial to syringe
- A61J1/2003—Accessories used in combination with means for transfer or mixing of fluids, e.g. for activating fluid flow, separating fluids, filtering fluid or venting
- A61J1/2006—Piercing means
- A61J1/201—Piercing means having one piercing end
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61J—CONTAINERS 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
- A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
- A61J1/14—Details; Accessories therefor
- A61J1/20—Arrangements for transferring or mixing fluids, e.g. from vial to syringe
- A61J1/2003—Accessories used in combination with means for transfer or mixing of fluids, e.g. for activating fluid flow, separating fluids, filtering fluid or venting
- A61J1/202—Separating means
- A61J1/2027—Separating means having frangible parts
Definitions
- the present invention relates to a container for separately containing two or more substances, and more particularly, to a separate storage container in which a solvent, such as a solution, in a storage chamber is fed into a solute containing member which contains a solute, such as a powered or liquid medicine, so that the solute, such as the powdered or liquid medicine, can be mixed and sterilely dissolved.
- a solvent such as a solution
- solute such as a powered or liquid medicine
- a suitable amount of a solution such as a physiological saline solution or 5 % grape sugar injection solution, is sucked in by means of an injector, and the needle of the injector is stuck into a solute vessel containing a powdered medicine, thereby injecting the solution. After the powdered medicine is dissolved, the solution is sucked in again to give a patient an injection.
- a solution such as a physiological saline solution or 5 % grape sugar injection solution
- a solute vessel containing a powdered medicine and a bag stuffed with a solution are sterilely connected by means.of an adapter which constitutes communication means holding a piercing needle and a frangible portion, the solution is injected into the solute vessel which contains the powdered medicine, thereby dissolving the powdered medicine, and the resulting solution is returned to the bag to subject a patient to an intravenous drip.
- a sleeve which is disposed so as to surround the piercing needle and is formed of a flexible material which expands and contracts as the needle moves.
- a solute vessel containing a powdered medicine, a bag stuffed with a solution, and an empty bag are sterilely connected to one another by means of an adapter which includes a needle and a frangible portion.
- the solution is put into the solute vessel to dissolve the powdered medicine, whereupon an antibiotic or the like is fully dissolved by using the empty bag as an air vent.
- the resulting solution is returned to the bag to subject a patient to an intravenous drip.
- vessels must be provided separately for the solution, injector, and powdered medicine, and must be operated in equipment for sterile work, such as a clean bench, so that the operation is troublesome, and there is a possibility of external bacterial contamination.
- equipment for sterile work such as a clean bench
- there is no need of the sterile equipment, such as a clean bench since no means is provided for positively keeping the prick portion of the solute vessel containing the powdered medicine separated from the piercing needle on the adapter when not in use in a normal state, so the solute vessel and the adapter may possibly be connected by mistake.
- the connecting operation is troublesome for an operator, and the construction of the adapter is complicated.
- the object of the present invention is to provide a medicine storage container which eliminates the various problems of the prior art separate storage containers described above, and which,despite its simple construction, can positively keep a piercing section of one containing member containing one substance separated from a piercing element capable of piercing the piercing section as required, when not in use in a normal state, and can enable an operator to perform the piercing operation easily and securely, when in use, so that a chamber for the one containing member and a chamber for the other containing member containing the other substance are sterilely connected to effect required mixing (dissolution), and which is easy to handle.
- the present invention is based on the common arrangement disclosed in the second and third prior art examples.
- the invention is premised on an arrangement which comprises a first containing member including a first chamber having a discharge port and containing a first substance therein; a second containing member containing second sub'stance and including a piercing section; and communication means including a piercing element capable of piercing the piercing section of the second containing member with a predetermined piercing resistance, as required, and a closing section extending into the first chamber and adapted normally to cut off the communication between the first chamber and the piercing element, the closing section being separable as required so that the communication is allowed when the closing section is separated, whereby sterile communication between the first and second chambers is effected as required.
- a separate storage container which is characterized by comprising: holding means disposed between the second containing member and the first chamber and surrounding the piercing element, and adapted normally to keep the piercing section of the second containing member and the piercing element separated and to undergo plastic deformation in the axial direction of the piercing element when subjected to an external force of a value grater than a predetermined value in the axial direction, thereby allowing the piercing element to pierce the piercing section and maintaining the pierced state, whereby the closing section of the communication means is separated after the piercing section is pierced by the piercing element, so that the sterile communication between the first and second chambers is effected through the communication means.
- the holding means can positively keep the piercing element of the communication means separated from the piercing section of the second containing member, so that an unexpected wrong piercing operation can be prevented.
- the holding means is plastically deformed by somewhat strongly applying the external force or an operator's manual force to a value greater than the predetermined value, so that the piercing operation can be effected, and the pierced state can be securely maintained by the plastically deformed holding means.
- the separate storage container of the present invention is simple in construction due to its few components, and its communicating portion, which constitute the communication means, is sealed to be kept sterile. Further, a guide cover, which constitutes the holding means, cannot be plastically deformed unless it is subjected to an axial external force of a value greater than the predetermined value, so that a piercing needle, which constitutes the piercing element of the communicating portion, can hardly be unexpectedly run through the piercing section by mistake. Since there is no empty bag or the like, moreover, the dissolving operation is easy.
- the predetermined value of the external force to subject the holding means to the plastic deformation is set to be greater than the piercing resistance of the piercing element piercing the piercing section, e.g., to 3 kgf or more, preferably within the range of 3 kgf to 5 kgf, further preferably to 3.5 kgf.
- the holding means is composed of a bellows-like guide cover integrally formed from thermoplastic resin by blow molding, for example.
- blow molding in particular, outwardly projecting crest portions of the bellows-like guide cover can be easily formed thinner than inwardly recessed bottom portions, so that a desirable property for the guide cover can be obtained.
- Figs. 1 to 4 show one embodiment of the present invention, in which Fig. 1 is a perspective view of a medicine storage container wrapped in a package, Fig. 2 is an enlarged perspective view of the medicine storage container with the package of Fig. 1 removed therefrom, Fig. 3 is an enlarged longitudinal sectional view of the medicine storage container shown in Fig. 2, especially portions corresponding to a guide cover and communication means and Fig. 4(a), 4(b), 4(c) and 4(d) are illustrative diagrams for individually showing states of operation of the medicine storage container; and
- Fig. 5 is a perspective view of a medicine storage container according to another embodiment of the present invention.
- Fig. 1 is a perspective view of a medicine storage container as a separate storage container of the present invention wrapped in a package
- Fig. 2 is a perspective view of the medicine storage container.
- numeral 1 denotes the medicine storage container
- the medicine storage container 1 comprises a storage chamber 2 and a housing chamber 3 which are integrally formed of a flexible synthetic resin sheet and are independent of each other.
- This medicine storage container 1 is entirely covered by a rectangular package 4, which ensures the stability of a solution S (mentioned later) for use as a solvent sealed in the storage chamber 2.
- the storage chamber 2 contains 50 to 100 ml of the solution S, e.g., a physiological saline solution or 5 % grape sugar solution.
- a discharge port 5 is provided at the lower portion of the storage chamber 2, and further, an aluminum cap 6 is fitted on the discharge port 5 so that the solution S cannot run out.
- a hole la which is used to hang the container 1 on a hanger 14 of a transfusion stand 13 mentioned later, is formed at one end portion of the container, and a boundary portion lb for dividing the two chambers 2 and 3 is formed at the middle portion.
- a communicating section 9 as communication means is disposed between the upper portion of the storage chamber 2 and the lower portion of the housing chamber 3.
- the communicating section 9 has a separable closing section 7 located in the storage chamber 2 and a bottle needle or piercing needle 8 as a piercing element at the distal end thereof which is located in the housing chamber 3.
- This communicating section is in the form of a cylinder closed at its end portion in the storage chamber 2, and a notch is formed in the inner peripheral surface so that the closing section 7 can be easily broken by means of an external force.
- the bottle needle 8 is provided with an angled edge 8a, which cannot be easily drawn out once it is passed through a piercing section 11 mentioned later. Further, the middle portion of the cylindrical communicating section 9 is held by means of the boundary portion lb.
- a glass or plastic vial or solute vessel 10, which constitutes a solute containing member, is housed in the housing chamber 3, and an antibiotic A as a powdered solute is contained in a chamber 10b in the vial 10.
- a mouth 10a of the vial 10 is fitted with a rubber stopper 11 for use as the piercing section through which the aforesaid bottle needle 8 can be run, and the stopper 11 is fixed by means of a mouthpierce lla (Fig. 3).
- a bellows-like guide cover 12 is provided between the mouth 10a of the vial 10 and a bottom portion 3a of the housing chamber 3 defined by the boundary portion lb as in Fig. 2. This guide cover 12 constitutes holding means.
- the guide cover 12 is formed of a material, e.g., a metal material such as aluminum or a thermoplastic resin such as polypropylene, which undergoes plastic deformation when subjected to an external force of a value greater than a predetermined value in the axial direction of the bottle needle 8, that is, in a direction such that the bottle needle 8 of the communicating section 9 pierces the rubber stopper 11 fitted in the mouth 10a of the vial 10, by an operator's hand, for example. Unless subjected to an axial force of a value greater than the predetermined value, therefore, the bottle needle 8 is kept at an off position, as shown in Fig. 3, in which it never pierces the rubber stopper 11, and the solution S cannot enter the vial 10 by mistake.
- a material e.g., a metal material such as aluminum or a thermoplastic resin such as polypropylene
- the bottle needle 8 is guided by the guide cover 12 so that it is prevented from misguidedly piercing any other object than the rubber stopper 11. Once the guide cover 12 is deformed and contracts, moreover, it maintains the deformed state as a result of the plastic deformation, so that the penetration of the bottle needle 8 can be secured.
- one end portion 12a of the guide cover 12 surrounds the mouth 10a of the vial and the rubber stopper 11 and is fixed to the vial 10.
- the other end portion 12b of the guide cover 12 extends in the axial direction of the bottle needle 8 so as to surround the needle, and is fixed to the bottom portion 3a.
- the guide cover 12 is blow-molded from the a thermoplastic resin, it can get better expansion and contraction because crest portions 12c of the guide cover 12, which project radially outward, are thinner than bottom portions 12d which are recessed radially inward, as shown in Fig. 3.
- the predetermined value of the external force which causes the plastic deformation of the guide cover 12 should be set to a value equal to or greater than the resistance against the needle 8 piercing the rubber stopper 11 of the vial 10, that is, piercing resistance.
- the predetermined value for the guide cover 12 is preferably set to 3 kgf as a minimum value.
- the upper limit of this predetermined value corresponds to the external force the operator can apply.
- the predetermined value is set within the range of 3 kgf to 5 kgf, preferably to 3.5 kgf.
- the guide cover 12 is formed from a metal material, the method of press-molding is preferably used.
- the package 4 covering the medicine storage container 1, as shown in Fig. 1, is removed.
- the bottle needle 8 of the communicating section 9 is run (see Fig. 4(a)) through the rubber stopper 11 in the mouth 10a of the vial 10 in the housing chamber 3 by axially contracting the guide cover 12 through plastic deformation by means of an external force of a value greater than the predetermined value.
- the closing section 7 of the communicating section 9 is broken or separated so that the vial 10 and the storage chamber 2 are caused to communicate by means of the communicating section 9 (see Fig. 4(b)).
- the solution S sealed in the storage chamber 2 is injected through the communicating section 9 into the vial 10 by holding the storage chamber 2 above the vial 10, whereby the powdered antibiotic A in the vial 10 is dissolved.
- the resulting solution of the powdered antibiotic A is returned to the storage chamber 2 by holding the vial 10 above the storage chamber 2. By repeating such operation, the powdered antibiotic A in the vial 10 is fully dissolved (see Fig. 4(c)).
- the medicine storage container 1 is hung on the hanger 14 of the transfusion stand 13 in a manner such that the hanger 14 is passed through the hole la of the medicine storage container 1 (see Fig. 4(d)).
- the medicine storage container 1 is hung on the hanger 14 so that the storage chamber 2, which contains the solution of the powdered antibiotic A, is on the bottom side.
- a transfusion set 15 comprises a bottle needle 16 piercing the discharge port 5, a drip cylinder 17, a clamp 18, an intravenous needle 19 to be stuck into a vein or the like of a patient M, and a tube 20 connecting these elements.
- the intravenous needle 19 of the transfusion set 15 is stuck into the vein or the like of the patient M, the bottle needle 16 is run through the discharge port 5 after removing the aluminum cap 6 fitted on the discharge port 5, and the clamp 18 is adjusted so that the solution of the powdered antibiotic A in the storage chamber 2 of the medicine storage container 1 can be administered to the patient M by an intravenous drip.
- the package 4 (Fig. 1) may be removed after the antibiotic A is dissolved in the solution S by the aforementioned piercing operation and before the setting on the transfusion stand 13.
- Fig. 5 shows another embodiment of the present invention. Since this embodiment is constructed substantially in the same manner as the embodiment shown in Fig. 2, like reference numerals are used to designate the same portions, and a description of those portions is omitted.
- the medicine storage container 1 comprises the storage chamber 2 and the housing chamber 3 which are integrally formed of the flexible synthetic resin sheet and are independent of each other. In the present embodiment, however, the storage chamber 2 and a housing chamber 30 are formed separately.
- the housing chamber 30 is in the form of a cylinder having a bellows-like portion 30a formed on the outer peripheral surface thereof.
- a hanging ring 21 is attached to an end face of the housing chamber 30.
- Other arrangements and functions of this embodiment are the same as those of the embodiment shown in Fig. 2, so that a description thereof is omitted.
- the bellows-like portion 30a serves to secure the axial plastic deformation of the guide cover 12 and the piercing state of the piercing element 8.
- the piercing section and the piercing element may be disposed on the storage-chamber side and on the solute-vessel side, respectively, in contrast with the arrangement of the storage chamber 2 and the solute vessel 10 disclosed in connection with the embodiments described above.
- various modifications may be effected in the present invention without departing from the spirit thereof, and the invention is not limited to the arrangements of the embodiments.
- the separate storage container according to the present invention is suitably used as a drip bag adapted to be connected to a transfusion set, whereby a medicine is administered to a patient by an intravenous drip.
- the separate storage container of the invention may be also widely utilized in other fields where powdered or liquid solutes, as well as medicines, must be sterilely dissolved in solvents.
- the present invention may be applied to any other fields than the medical field in which medicines and the like are handled.
- the medicine storage container is disclosed as an example of the separate storage container of the present invention, in connection with the embodiments, the range of application of the invention is not limited to the field associated with "medicines" in a narrow sense.
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- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medical Preparation Storing Or Oral Administration Devices (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP243080/87 | 1987-09-28 | ||
JP24308087A JPS6485653A (en) | 1987-09-28 | 1987-09-28 | Drug receiving container |
PCT/JP1988/000980 WO1989002730A1 (en) | 1987-09-28 | 1988-09-27 | Separate storage container |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0395758A1 true EP0395758A1 (de) | 1990-11-07 |
EP0395758A4 EP0395758A4 (en) | 1990-12-27 |
EP0395758B1 EP0395758B1 (de) | 1994-07-20 |
Family
ID=17098480
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP88908369A Expired - Lifetime EP0395758B1 (de) | 1987-09-28 | 1988-09-27 | Behälter für getrennte lagerung |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP0395758B1 (de) |
JP (1) | JPS6485653A (de) |
DE (1) | DE3850781T2 (de) |
WO (1) | WO1989002730A1 (de) |
Cited By (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1993002724A1 (en) * | 1991-07-30 | 1993-02-18 | Baxter International Inc. | Needleless vial access device |
EP0536841A1 (de) * | 1991-10-07 | 1993-04-14 | INGE S.p.A. | Mischbehälter mit Irrigator für einmalige Verwendung |
EP0538891A1 (de) * | 1991-10-25 | 1993-04-28 | Fujisawa Pharmaceutical Co., Ltd. | Infusionsbehälter |
EP0554988A1 (de) * | 1992-02-04 | 1993-08-11 | Material Engineering Technology Laboratory, Inc. | Vorrichtung zum Vermischen |
DE4314090A1 (de) * | 1993-04-29 | 1994-11-03 | Wolfgang Dr Vilmar | Medizinisches Besteck zur Herstellung einer Medikamentenlösung |
GB2327409A (en) * | 1997-07-16 | 1999-01-27 | Inibsa Lab | A cartridge |
US5976115A (en) * | 1997-10-09 | 1999-11-02 | B. Braun Medical, Inc. | Blunt cannula spike adapter assembly |
WO2005030111A1 (en) | 2003-09-30 | 2005-04-07 | Coloplast A/S | A wound care device |
US7520919B2 (en) | 2004-06-22 | 2009-04-21 | Gambro Lundia Ab | Transducer-protector device for medical apparatus |
US8022375B2 (en) | 2003-12-23 | 2011-09-20 | Baxter International Inc. | Method and apparatus for validation of sterilization |
US8226627B2 (en) | 1998-09-15 | 2012-07-24 | Baxter International Inc. | Reconstitution assembly, locking device and method for a diluent container |
WO2013020989A1 (en) | 2011-08-11 | 2013-02-14 | Fresenius Medical Care Deutschland Gmbh | Container for dialysis |
US20150005734A1 (en) * | 2011-12-29 | 2015-01-01 | Otsuka Pharmaceutical Factory, Inc. | Exposure prevention cover, exposure prevention cover module provided with same, drug solution supply system, and drug solution supply method |
EP2962676A1 (de) | 2014-07-02 | 2016-01-06 | Paolo Gobbi Frattini S.r.l. | Flexible verpackung mit abgedichteter steriler kammer zur rekonstitution und verabreichung von flüssigen, in den körper eines patienten einflössbaren medizinischen substanzen oder nährstoffsubstanzen |
US9527627B2 (en) | 2011-05-18 | 2016-12-27 | Fresenius Medical Care Deutschland Gmbh | Connector for dialysis container, container equipped with such connector, manufacturing and filling method for such connectors and containers |
US9724078B2 (en) | 2013-06-21 | 2017-08-08 | Ferrosan Medical Devices A/S | Vacuum expanded dry composition and syringe for retaining same |
US9999703B2 (en) | 2012-06-12 | 2018-06-19 | Ferrosan Medical Devices A/S | Dry haemostatic composition |
US10111980B2 (en) | 2013-12-11 | 2018-10-30 | Ferrosan Medical Devices A/S | Dry composition comprising an extrusion enhancer |
EP3427781A3 (de) * | 2017-07-11 | 2019-05-01 | Pharma Resources GmbH | Arzneimittel und vorrichtungssystem für druckbeaufschlagte aerosoltherapien in einem säugetierhohlraum |
EP3355847A4 (de) * | 2015-09-29 | 2019-07-03 | Siemens Medical Solutions USA, Inc. | Aseptisches zusammensetzen von pharmazeutischen behältern |
US10653837B2 (en) | 2014-12-24 | 2020-05-19 | Ferrosan Medical Devices A/S | Syringe for retaining and mixing first and second substances |
CN112020345A (zh) * | 2018-04-13 | 2020-12-01 | 费森尤斯卡比股份公司 | 提供用于肠外营养物的制剂的设备和方法 |
CN112020344A (zh) * | 2018-04-13 | 2020-12-01 | 费森尤斯卡比股份公司 | 用于混合系统的容器、用于肠外营养物的混合系统以及混合方法 |
US10918796B2 (en) | 2015-07-03 | 2021-02-16 | Ferrosan Medical Devices A/S | Syringe for mixing two components and for retaining a vacuum in a storage condition |
US11046818B2 (en) | 2014-10-13 | 2021-06-29 | Ferrosan Medical Devices A/S | Dry composition for use in haemostasis and wound healing |
US11109849B2 (en) | 2012-03-06 | 2021-09-07 | Ferrosan Medical Devices A/S | Pressurized container containing haemostatic paste |
US11801324B2 (en) | 2018-05-09 | 2023-10-31 | Ferrosan Medical Devices A/S | Method for preparing a haemostatic composition |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3834566A1 (de) * | 1988-10-11 | 1990-04-12 | Fresenius Ag | Behaelter zur sterilen, getrennten aufbewahrung mindestens zweier substanzen und zur vermischung derselben |
JPH077965Y2 (ja) * | 1990-11-14 | 1995-03-01 | 昭和電工株式会社 | 輸液バッグ |
US5776125A (en) | 1991-07-30 | 1998-07-07 | Baxter International Inc. | Needleless vial access device |
JP3146465B2 (ja) * | 1992-03-13 | 2001-03-19 | 株式会社ニッショー | 薬液注入装置 |
JP3256583B2 (ja) * | 1992-12-10 | 2002-02-12 | 株式会社リコー | 電子写真用トナー及びその製法 |
US5547797A (en) * | 1993-08-05 | 1996-08-20 | Minolta Co., Ltd. | Developer for developing electrostatic latent images |
US6071270A (en) | 1997-12-04 | 2000-06-06 | Baxter International Inc. | Sliding reconstitution device with seal |
AR021220A1 (es) | 1998-09-15 | 2002-07-03 | Baxter Int | DISPOSITIVO DE CONEXIoN PARA ESTABLECER UNA COMUNICACIoN FLUíDA ENTRE UN PRIMER RECIPIENTE Y UN SEGUNDO RECIPIENTE. |
DE10005813A1 (de) * | 2000-02-10 | 2001-08-23 | Wolfgang Vilmar | Mischbesteck |
AU2002367086B2 (en) * | 2001-12-21 | 2008-08-21 | Ferrosan Medical Devices A/S | A hemostatic kit, a method of preparing a hemostatic agent and a method of promoting hemostasis |
US7923431B2 (en) | 2001-12-21 | 2011-04-12 | Ferrosan Medical Devices A/S | Haemostatic kit, a method of preparing a haemostatic agent and a method of promoting haemostatis |
CN1739017B (zh) | 2002-12-11 | 2011-04-06 | 弗罗桑医疗设备公司 | 用作拭子的基于明胶的材料 |
US7048724B2 (en) * | 2002-12-17 | 2006-05-23 | Denver Biomedicals, Inc. | Device for withdrawing body fluids |
WO2005072700A2 (en) | 2004-01-30 | 2005-08-11 | Ferrosan A/S | Haemostatic sprays and compositions |
DE102004021990B3 (de) * | 2004-05-04 | 2005-11-10 | Fresenius Kabi Deutschland Gmbh | Medizinischer Behälter zum Verabreichen einer Flüssigkeit aus einer Trägerlösung und einem zugemischten Medikament |
CN101001649B (zh) | 2004-07-09 | 2011-08-31 | 弗罗桑医疗设备公司 | 包括透明质酸的止血组合物及其制备方法 |
WO2007136791A2 (en) | 2006-05-18 | 2007-11-29 | Maej, Llc | Delivery device with separate chambers connectable in fluid communication when ready for use, and related method |
EP2259803B2 (de) | 2008-02-29 | 2019-03-13 | Ferrosan Medical Devices A/S | Vorrichtung zur förderung von hämostase und/oder wundheilung |
JP7003493B2 (ja) * | 2017-08-28 | 2022-02-04 | ニプロ株式会社 | 透析液分析用標準試薬キット |
JP6642339B2 (ja) * | 2016-08-30 | 2020-02-05 | ニプロ株式会社 | 透析液分析用標準試薬キット |
US20190192556A1 (en) * | 2016-08-30 | 2019-06-27 | Nipro Corporation | Standard reagent kit for analysis of dialysis fluid, and aqueous solutions for standard reagent, dialysis fluid and substitution fluid for artificial kidney |
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JPS61260772A (ja) * | 1985-05-14 | 1986-11-18 | Mitsubishi Electric Corp | 画像欠陥補償装置 |
JPH0614708Y2 (ja) * | 1989-10-17 | 1994-04-20 | ホシザキ電機株式会社 | 飲料の保温・保冷装置 |
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1988
- 1988-09-27 EP EP88908369A patent/EP0395758B1/de not_active Expired - Lifetime
- 1988-09-27 DE DE3850781T patent/DE3850781T2/de not_active Expired - Fee Related
- 1988-09-27 WO PCT/JP1988/000980 patent/WO1989002730A1/ja active IP Right Grant
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Cited By (37)
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US5411499A (en) * | 1988-01-25 | 1995-05-02 | Baxter International Inc. | Needleless vial access device |
WO1993002724A1 (en) * | 1991-07-30 | 1993-02-18 | Baxter International Inc. | Needleless vial access device |
EP0536841A1 (de) * | 1991-10-07 | 1993-04-14 | INGE S.p.A. | Mischbehälter mit Irrigator für einmalige Verwendung |
US5383579A (en) * | 1991-10-07 | 1995-01-24 | Inge, S.P.A. | Container for containing two flowable materials in separated compartments, but permitting the two materials to be mixed for dispensing, before the container is opened |
EP0538891A1 (de) * | 1991-10-25 | 1993-04-28 | Fujisawa Pharmaceutical Co., Ltd. | Infusionsbehälter |
US5352191A (en) * | 1991-10-25 | 1994-10-04 | Fujisawa Pharmaceutical Co., Ltd. | Transfusion device |
EP0554988A1 (de) * | 1992-02-04 | 1993-08-11 | Material Engineering Technology Laboratory, Inc. | Vorrichtung zum Vermischen |
US5380315A (en) * | 1992-02-04 | 1995-01-10 | Material Engineering Technology Laboratory Incorporated | Mixing apparatus |
DE4314090A1 (de) * | 1993-04-29 | 1994-11-03 | Wolfgang Dr Vilmar | Medizinisches Besteck zur Herstellung einer Medikamentenlösung |
GB2327409B (en) * | 1997-07-16 | 1999-09-15 | Inibsa Lab | A cartridge |
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US5976115A (en) * | 1997-10-09 | 1999-11-02 | B. Braun Medical, Inc. | Blunt cannula spike adapter assembly |
US8226627B2 (en) | 1998-09-15 | 2012-07-24 | Baxter International Inc. | Reconstitution assembly, locking device and method for a diluent container |
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US8022375B2 (en) | 2003-12-23 | 2011-09-20 | Baxter International Inc. | Method and apparatus for validation of sterilization |
US7520919B2 (en) | 2004-06-22 | 2009-04-21 | Gambro Lundia Ab | Transducer-protector device for medical apparatus |
US9527627B2 (en) | 2011-05-18 | 2016-12-27 | Fresenius Medical Care Deutschland Gmbh | Connector for dialysis container, container equipped with such connector, manufacturing and filling method for such connectors and containers |
US10022299B2 (en) | 2011-08-11 | 2018-07-17 | Fresenius Medical Care Deutschland Gmbh | Container for dialysis |
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US10010481B2 (en) | 2014-07-02 | 2018-07-03 | Paolo Gobbi Frattini S.R.L. | Flexible package with a sealed sterile chamber for the reconsitution and administration of fluid medicinal or nutritional substances instillable into the body of a patient |
US11046818B2 (en) | 2014-10-13 | 2021-06-29 | Ferrosan Medical Devices A/S | Dry composition for use in haemostasis and wound healing |
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US11801324B2 (en) | 2018-05-09 | 2023-10-31 | Ferrosan Medical Devices A/S | Method for preparing a haemostatic composition |
Also Published As
Publication number | Publication date |
---|---|
EP0395758A4 (en) | 1990-12-27 |
JPS6485653A (en) | 1989-03-30 |
DE3850781T2 (de) | 1995-02-23 |
JPH0236261B2 (de) | 1990-08-16 |
DE3850781D1 (de) | 1994-08-25 |
WO1989002730A1 (en) | 1989-04-06 |
EP0395758B1 (de) | 1994-07-20 |
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