WO1998033449A1 - Contenant pour liquide intraveineux - Google Patents
Contenant pour liquide intraveineux Download PDFInfo
- Publication number
- WO1998033449A1 WO1998033449A1 PCT/US1998/001742 US9801742W WO9833449A1 WO 1998033449 A1 WO1998033449 A1 WO 1998033449A1 US 9801742 W US9801742 W US 9801742W WO 9833449 A1 WO9833449 A1 WO 9833449A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- moulding
- container
- port
- tubes
- blow
- Prior art date
Links
- 239000003978 infusion fluid Substances 0.000 title claims abstract description 18
- 239000007924 injection Substances 0.000 claims abstract description 42
- 238000002347 injection Methods 0.000 claims abstract description 42
- 238000007789 sealing Methods 0.000 claims abstract description 24
- 238000000071 blow moulding Methods 0.000 claims abstract description 23
- 230000015572 biosynthetic process Effects 0.000 claims abstract description 20
- 238000005755 formation reaction Methods 0.000 claims abstract description 20
- 238000007664 blowing Methods 0.000 claims abstract description 4
- 238000000465 moulding Methods 0.000 claims description 52
- 238000000034 method Methods 0.000 claims description 28
- 230000002093 peripheral effect Effects 0.000 claims description 23
- 238000001746 injection moulding Methods 0.000 claims description 20
- 239000000463 material Substances 0.000 claims description 14
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 230000000694 effects Effects 0.000 claims description 6
- 230000004927 fusion Effects 0.000 claims description 5
- 238000002788 crimping Methods 0.000 claims description 2
- 238000010276 construction Methods 0.000 abstract description 7
- 230000009977 dual effect Effects 0.000 description 3
- 239000012528 membrane Substances 0.000 description 2
- 238000004891 communication Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000012768 molten material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
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
- A61J1/05—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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C49/00—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor
- B29C49/20—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor of articles having inserts or reinforcements ; Handling of inserts or reinforcements
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C49/00—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor
- B29C49/20—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor of articles having inserts or reinforcements ; Handling of inserts or reinforcements
- B29C2049/2008—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor of articles having inserts or reinforcements ; Handling of inserts or reinforcements inside the article
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C49/00—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor
- B29C49/20—Blow-moulding, i.e. blowing a preform or parison to a desired shape within a mould; Apparatus therefor of articles having inserts or reinforcements ; Handling of inserts or reinforcements
- B29C2049/2021—Inserts characterised by the material or type
- B29C2049/2047—Tubular inserts, e.g. tubes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2031/00—Other particular articles
- B29L2031/712—Containers; Packaging elements or accessories, Packages
- B29L2031/7148—Blood bags, medical bags
Definitions
- THIS INVENTION relates to a container for intravenous fluid. It relates also to a method of manufacturing such a container, and to moulding apparatus suitable for use in carrying out the method of the invention.
- a container for intravenous fluid which is hollow, which is in the form of a moulding of semi-rigid polymeric material, and which has two separate ports, an administration port and an injection port, which are integral with a bag portion of the container .
- Each of said two ports may advantageously have sealing formations for hermetically sealing it at two positions spaced along the length of each respective port.
- Said bag portion may be of blow-moulded manufacture .
- the administration port may comprise an outer tube integral with a wall of the bag portion and a sealing diaphragm hermetically sealing the administration port, the outer tube having a free end portion adapted to be fused into a hermetic seal.
- the administration port may comprise a tubular insert received in leak-tight manner within the outer tube, the insert including said sealing diaphragm. Then, a wall of the insert may be fused to a wall of the outer tube.
- the wall of the insert may have one or more peripheral sealing ridges .
- the insert may be received tightly within the outer tube in the manner of a crimp fit.
- sealing formations may be provided at the sealing interface.
- the sealing formations may be in the form of one or more peripheral ridges .
- the insert may be in the form of a moulding.
- the diaphragm may be integrally moulded with its wall. It may be of rigid construction.
- the injection port may comprise an outer tube integral with a wall of the bag portion, a stopper seat defined inside the tube, and a stopper adapted for sealing receipt in the seat, the outer tube having a free end portion adapted to be fused into a hermetic seal.
- the seat may be enveloped or surrounded by the outer tube.
- a wall of said outer tube of the injection port may be stepped forming an inner shoulder to define the stopper seat.
- the seat may be provided in an insert which is sealingly received within the outer tube of the injection port.
- the respective outer tubes may each have a peripheral line of weakness toward their respective free end portions to facilitate opening the respective tube in use by breaking or severing or tearing off the hermetically sealed end portion.
- a method of moulding a container for intravenous fluid including moulding one end portion of a bag portion of the container; moulding two tubes to form respectively an administration port and an injection port adjacent each other, each tube being integral with and extending from said one end portion of the bag portion, and having a mouth opening into the bag portion; forming an integral hermetic seal in the mouth of the administration port, the mouth of the injection port being open; moulding the bag portion integrally with said one end portion of the bag portion by blow moulding, blowing taking place via said injection port.
- moulding said end portion of the bag portion and said two tubes may be by injection moulding.
- the method may include forming lines of weakness toward end portions of the tubes, the method including pinching or crimping the tubes to render walls of the tubes thin to form the lines of weakness after the tubes have been formed and before the material forming the tubes has completely set. This has the advantage that moulding material for the respective end portion has been injected and passed beyond the location of the lines of weakness before the cross-sectional area is decreased.
- the method may include moulding a step forming an internal annular seat for a bung or stopper in the tube of the injection port.
- the method may include forming a pari ⁇ on integrally with said end portion of said bag portion, said moulding the bag portion by blow moulding being from said parison.
- Injection moulding of said end portion of the bag portion may be effected at an injection moulding station and blow moulding may be effected at a blow moulding station, the method including relocating the moulding from the injection moulding station when it has frozen to an appropriate degree, to the blow moulding station, and commencing injection moulding in respect of a succeeding container while blow moulding is taking place in respect of the preceding container. In this manner, injection moulding apparat s is used and is thus not idle while blow moulding takes place. This enhances production capacity.
- the method when it does not include injection moulding steps may include providing a parison, and moulding said two tubes may be effected by closing a pair of port platens over an end portion of the parison, inserts or cores being provided to form openings of the tubes, and moulding the bag portion may be effected by closing a pair of bag platens over a portion of the parison adjacent said end portion of the parison.
- the method may include holding one or more cores or inserts between the port platens prior to forming of the tubes, and moulding said one or more cores or inserts into the respective outer tubes when the outer tubes are moulded.
- Holding of a core or an insert in respect of the injection port may be by means of a blow nozzle provided to blow air under pressure into the parison to effect blow moulding.
- the method may include supplying energy to cause plasticization to cause fusion of the insert (s) into the respective outer tube(s) .
- the method may include forming lines of weakness toward ends of the tubes during moulding to facilitate breaking end portions of the tubes off in use.
- a moulding apparatus suitable for use in manufacturing a container for intravenous fluid by moulding, the apparatus comprising a pair of port platens having port moulding cavities and holders for holding cores inside the port moulding cavities to mould an administration port and injection port of the container, the holder of the administration port being adapted to hold its core shy of a ' all of the port platens to cause a sealing diaphragm to be formed in the administration port, the holder of the injection port being adapted to hold its core against a wall of the port platen to cause the injection port to be open; a pair of bag platens for enclosing a parison and a blow nozzle arranged to blow through the injection port to form a bag portion of the container by blow moulding.
- the pair of port platens may form part of injection moulding apparatus.
- a container containing intravenous fluid the container being a container in accordance with the first aspect of this invention.
- Figure 1 shows, in frontal elevation, a first embodiment of a container for intravenous fluid in accordance with the invention
- Figure 2 shows, to a larger scale, in section, an administration port and an injection port of the container of Figure 1;
- Figure 3 shows, fragmentarily, in section, to yet a larger scale, an insert forming part of an injection port of a variant of the embodiment of Figure 1;
- Figure 4 corresponds to Figure 3 but shows yet a further variant of the insert
- Figure 5 shows, in frontal sectional elevation, a first embodiment of moulding apparatus in accordance with the invention
- Figure 6 shows, in end view along lines VI-VI of Figure 5 , one half of the moulding apparatus of Figure 5 ;
- Figure 7 shows a plan view of the moulding apparatus of Figure 5;
- Figures 8 and 9 show, respectively in part sectional, front view and in side view, a second embodiment of a container for intravenous fluid in accordance with the invention; and Figure 10 shows, in front view, fragmentarily, injection moulding apparatus forming part of a second etnbodiment of moulding apparatus in accordance with the invention.
- a first embodiment of a container for intravenous fluid in accordance with the invention is generally indicated by reference numeral 10.
- the container 10 comprises a container body or bag portion 12 having, at one end thereof which will be a lower end when in use, but which is shown as an upper end in the drawings, an administration port 14, and an injection port 16.
- the ports are described in more detail ⁇ with reference to Figure 2.
- the administration port 14 comprises an outer tube 22 integral with the wall defining the bag portion 12.
- the outer tube 22 has peripheral formations 24, more specifically inner peripheral formations, to effect sealing as will be described hereinafter. Beyond the inner peripheral formations 24, it has a peripheral line of weakness 26 to allow a free end portion of the outer tube 22 to be torn off when the container 10 is to be used.
- An end of the outer tube 22 is fused to form an hermetic seal as shown at 28.
- insert 30 Inserted in the outer tube 22 in the region proximate the top of the container body 12, is an internal insert 30 comprising an internal diaphragm 32.
- the insert 30 is generally in the form of a tube of rigid, pre-moulded material. It has outer peripheral formations 34 complemental to the inner peripheral formations 24 of the outer tube 22.
- the insert 30 is merely tightly gripped within the outer tube 22 and friction between the peripheral formations 24 and 34 effect sealing.
- the peripheral formations are fused together to effect a positive seal.
- the injection port 16 similarly comprises an outer tube 42 integral with and in communication with the container body 12 via a wall thereof .
- the outer tube 42 has a step providing an internal, axially outwardly directed shoulder 44. Spaced beyond the step, there is provided a peripheral line of weakness 46 to allow a free end portion of the outer tube 42 to be torn off.
- a stop per 50 conveniently of a polymeric material, which is advantageously at least slightly resilient, is tightly, frictionally, received within the outer tube 42 and seats on the internal shoulder 44 which provides a seat for the stopper 50.
- the free end of the outer tube 42 is then fused to form a hermetic seal as shown at 48.
- the seal 28 at the end of the outer tube 22 of the administration port 14 can be formed at the time the seal 48 is formed.
- an insert 52 is receivable within an outer tube corresponding to the outer tube 42 of the injection port but not having the step 44.
- the insert 52 has a wall 54 having an internal step providing an internal, axially outwardly directed shoulder 58 corresponding to the shoulder 44 and which forms a seat for the stopper 50.
- the wall 54 has outer peripheral formations 56 complemental to inner peripheral formations provided in the outer tube corresponding to the inner peripheral formations 24 of the outer tube 22 of the administration port 14.
- the insert 52 as was described for the insert
- the outer peripheral formations 56 are fused with the outer tube 42 to provide a positive seal.
- energy for example in the form of heat, or of ultra-sonic waves, is applied to the peripheral formations 56 to plasticize them to form peripheral areas 56.1 of molten material to effect fusing.
- a similar insert 52 is shown in which a thinner wall area 54.1 is provided intermediate the two outer peripheral formations 56. Under construction, energy is applied to the thinner area 54.1 to plasticize it and to cause fusion to an outer tube.
- insert 30 can be fused in similar manner into the outer tube 22 of the administration port 14.
- a first embodiment of moulding apparatus for moulding the container 10 by means of blow moulding is generally indicated by reference numeral 60.
- the moulding apparatus 60 comprises a first pair of platens 62, respectively having shaped concave formations 64 co-operating, when the platens 62 have been closed onto each other, to form a cavity within which the container body or bag portion 12 is blow-moulded.
- Tops of the platens 62 are flat and in line as indicated by reference numeral 66.
- a pair of second platens 68 is provided immediately above the pair of first platens 62.
- the second platens 68 respectively have concave shaped faces 70 defining a concave moulding cavity to form an upper portion of the container body or bag portion 12 as well as the administration port 14 and injection port 16.
- Extending above the faces 60 as can best be seen in Figures 6 and 7, there are provided secondary moulding cavities generally indicated by reference numeral 72 in Figure 7 and including half-circular cylindrical grooves 74 by means of which the outer tubes 22 and 42 respectively of the administration port 14 and injection port 16 are formed.
- the first platens 62 and the second platens 68 align very well when closed to ensure smooth blending of the upper portion and the lower portion of the container.
- a parison station a parison in heated state so as to be plastic, with a lower end thereof sealed, is dropped in position in between the first platens 62.
- the parison is somewhat inflated to ensure that its ' wall is smooth and so that portions of the wall do not cling to one another.
- the platens 62 are closed and the parison is severed by means of a "hot knife" to be of appropriate length.
- a blow nozzle or blow pin and a dummy pin are positioned inside the open mouth of the parison and the platens 68 are closed while the parison is dilated by means of air under pressure against the mould surfaces to form the container.
- the outer tubes 22 and 42 are formed around the blow pin and the dummy pin by means of the cylindrical grooves 74.
- the insert 30 (which is sealed as shown at 32) is held over the dummy blow nozzle or pin during closing in of the second platens 68 thus to mould the insert 30 into the outer tube 22.
- the insert 52 (which is open) can be held ' in like manner on the blow nozzle 82 to be mounted into the outer tube 42.
- the blow moulding process is in practice, in general, automatic.
- the tube of molten plastic material forming the parison will be dropped from a nozzle at a first station, i.e. the parison station.
- the platens 62 close onto it to pinch the parison as described above, the parison then being cut to length.
- the mould then rapidly moves away to a second station or blow station where a blow pin is inserted in the open end of the parison and the parison is then dilated under high pressure to fill the mould cavity as described above. Pressure is maintained until the material has frozen and sufficiently cooled down.
- a third station is provided where the insert 30, and if applicable also the insert 52, are ' automatically picked up and held in position so that closing in of the second platens 68 will form the outer tubes as described above.
- An energizing station is provided to apply energy, for example in the form of heat, or in the form of ultra-sonic waves, to heat the portions of the or each insert as described with reference to Figures 3 and 4 to allow fusion.
- Either energy can be applied from externally of the insert to achieve the situation as sketched in Figure 3, or the energy can be applied from internally of the insert to achieve the situation as described with reference to Figure 4.
- the administration port is sealed positively by means of the insert 30 and its internal membrane 32 during forming of the container body i.e. prior to filling thereof. It is to be appreciated that the integrity of the hermetic sealing of the insert 30 in the outer tube 24 is not of crucial importance because the end of the outer tube is fused as shown at 28.
- FIG. 110 Another embodiment of a container for containing intravenous fluid is generally indicated by reference numeral 110.
- the container 110 is similar in many respects to the container 10 described above. Furthermore, generally, like reference numerals are used to refer to like components or features. The embodiment 110 is not again described in detail and emphasis is merely placed on differences to the embodiment 10.
- an upper portion of a bag portion 112 of the container 110 as well as an administration port 114 and an injection port 116 are formed by injection moulding. Subsequently, the major portion of the bag portion 112 is formed by blow moulding.
- Injection moulding components for performing the injection moulding are generally indicated by reference numeral 170 in Figure 10.
- the components 170 comprise a peripheral gate member 170.1 defining a gate 170.2 within which a former member 170.3 is received with clearance to define a peripheral feeding passage 170.4.
- a pair of injection moulds of which one only is shown in Figure 10 indicated by reference numeral 168.
- the mould 168 together with complemental moulding cavities in the complemental mould, defines a moulding cavity 174 for the administration port 114, and a moulding cavity 174.1 for the injection port 116.
- a core 175 is received within the pair of moulds 168 extending centrally within the opposing mould cavities 174 with clearance to cause an outer tube 122 to be formed. It is significant that the core 175 is checked shy of the former member 170.3 to cause a sealing membrane to be formed integrally with the tube at the point where the tube enters the bag portion.
- a core 175.1 has a step as indicated by reference numeral 175.2 which, in conjunction with a step 144.1 in the moulding cavity 174.1, causes an annular shoulder or seat 144 shown in Figure 8 to be formed in the tube 142 forming the injection port 116.
- the core 175.1 extends into the former member 170.3 to ensure that the tube 142 is open-ended.
- a pair of lugs or wings 127, 147 is formed toward the free end of each of the tubes 122 and 144 i.e. immediately above lines of weakness 126, 146 to enable the respective tubes 122,
- the respective tubes 122, 142 extend to allow end portions thereof easily to be fused as indicated by reference numerals 128 and 148 during the course of manufacture .
- the seal 128 can be formed during moulding of the bag, it may conveniently be done in conjunction with forming the seal 148 after the container has been filled with intravenous fluid and before it is sterilized in an autoclave or the like.
- the position for a stopper is indicated in chain- dot lines in Figure 8 indicated by reference numeral 150.
- the stopper 150 will be seated on the seat 144 after filling.
- the lines of weakness 126, 146 are formed ideally after the material for the wings 127, 147 and the free end portions of the tubes 122, 142 have passed the positions of the lines of weakness.
- pinching devices are provided, conveniently mounted in fixed positions relative to the moulds 168, to be operated to perform pinching actions after the material has been injected, and before the material has frozen.
Landscapes
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Mechanical Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Hematology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medical Preparation Storing Or Oral Administration Devices (AREA)
- Blow-Moulding Or Thermoforming Of Plastics Or The Like (AREA)
Abstract
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU61378/98A AU6137898A (en) | 1997-02-03 | 1998-01-30 | Container for intravenous fluid |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ZA97865 | 1997-02-03 | ||
ZA97/0865 | 1997-02-03 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1998033449A1 true WO1998033449A1 (fr) | 1998-08-06 |
Family
ID=25586185
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1998/001742 WO1998033449A1 (fr) | 1997-02-03 | 1998-01-30 | Contenant pour liquide intraveineux |
Country Status (3)
Country | Link |
---|---|
AU (1) | AU6137898A (fr) |
WO (1) | WO1998033449A1 (fr) |
ZA (1) | ZA98701B (fr) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2012126925A1 (fr) * | 2011-03-22 | 2012-09-27 | Thomas Nicola | Poche médicale |
EP2845576A4 (fr) * | 2012-02-17 | 2016-03-02 | Chongqing Lummy Pharmaceutical | Récipient de transfusion à deux têtes |
US20220040042A1 (en) * | 2019-01-18 | 2022-02-10 | West Pharma. Services, IL, Ltd. | Liquid transfer devices for use with intravenous (iv) bottles |
WO2023238145A1 (fr) * | 2022-06-08 | 2023-12-14 | Jedux Parenteral Private Limited | Récipient en polypropylène pour fluide intraveineux |
WO2025170674A1 (fr) * | 2024-02-06 | 2025-08-14 | Baxter International Inc. | Système de récipient de solution de dialyse péritonéale moulé par injection-étirage-soufflage |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2894510A (en) * | 1954-02-25 | 1959-07-14 | Fenwal Lab Inc | Sealing closures for fluid containers |
US3342179A (en) * | 1965-06-18 | 1967-09-19 | Abbott Lab | Blood collection and sampling apparatus having separable coupling means |
US3752627A (en) * | 1969-06-18 | 1973-08-14 | Sidel Sa | Device for manufacturing a hollow article of plastic material |
US3765813A (en) * | 1970-01-15 | 1973-10-16 | L Moore | Blow molding apparatus |
US3860683A (en) * | 1972-07-27 | 1975-01-14 | Dennis H Ward | Method for blow molding an article having a re-entrant portion |
US4439192A (en) * | 1975-05-30 | 1984-03-27 | Stichting Centraal Laboratorium Van De Bloedtransfusiedienst Van Het Nederlandse Rode Kruis | Container for liquids for use in medicine and surgery |
US5226564A (en) * | 1986-11-28 | 1993-07-13 | E. R. Squibb & Sons, Inc. | Manufacture of bags |
US5651776A (en) * | 1995-03-22 | 1997-07-29 | Angiodynamics, Inc. | Luer-type connector |
-
1998
- 1998-01-28 ZA ZA98701A patent/ZA98701B/xx unknown
- 1998-01-30 WO PCT/US1998/001742 patent/WO1998033449A1/fr active Application Filing
- 1998-01-30 AU AU61378/98A patent/AU6137898A/en not_active Abandoned
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2894510A (en) * | 1954-02-25 | 1959-07-14 | Fenwal Lab Inc | Sealing closures for fluid containers |
US3342179A (en) * | 1965-06-18 | 1967-09-19 | Abbott Lab | Blood collection and sampling apparatus having separable coupling means |
US3752627A (en) * | 1969-06-18 | 1973-08-14 | Sidel Sa | Device for manufacturing a hollow article of plastic material |
US3765813A (en) * | 1970-01-15 | 1973-10-16 | L Moore | Blow molding apparatus |
US3860683A (en) * | 1972-07-27 | 1975-01-14 | Dennis H Ward | Method for blow molding an article having a re-entrant portion |
US4439192A (en) * | 1975-05-30 | 1984-03-27 | Stichting Centraal Laboratorium Van De Bloedtransfusiedienst Van Het Nederlandse Rode Kruis | Container for liquids for use in medicine and surgery |
US5226564A (en) * | 1986-11-28 | 1993-07-13 | E. R. Squibb & Sons, Inc. | Manufacture of bags |
US5651776A (en) * | 1995-03-22 | 1997-07-29 | Angiodynamics, Inc. | Luer-type connector |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2012126925A1 (fr) * | 2011-03-22 | 2012-09-27 | Thomas Nicola | Poche médicale |
CN103841944A (zh) * | 2011-03-22 | 2014-06-04 | 托马斯·尼古拉 | 医疗袋 |
CN103841944B (zh) * | 2011-03-22 | 2017-03-22 | 托马斯·尼古拉 | 医疗袋 |
EP2845576A4 (fr) * | 2012-02-17 | 2016-03-02 | Chongqing Lummy Pharmaceutical | Récipient de transfusion à deux têtes |
US20220040042A1 (en) * | 2019-01-18 | 2022-02-10 | West Pharma. Services, IL, Ltd. | Liquid transfer devices for use with intravenous (iv) bottles |
US12427091B2 (en) * | 2019-01-18 | 2025-09-30 | West Pharma. Services IL, Ltd. | Liquid transfer devices for use with intravenous (IV) bottles |
WO2023238145A1 (fr) * | 2022-06-08 | 2023-12-14 | Jedux Parenteral Private Limited | Récipient en polypropylène pour fluide intraveineux |
WO2025170674A1 (fr) * | 2024-02-06 | 2025-08-14 | Baxter International Inc. | Système de récipient de solution de dialyse péritonéale moulé par injection-étirage-soufflage |
Also Published As
Publication number | Publication date |
---|---|
ZA98701B (en) | 1998-08-05 |
AU6137898A (en) | 1998-08-25 |
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