EP2826458A1 - Capuchon pour ampoule - Google Patents

Capuchon pour ampoule Download PDF

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Publication number
EP2826458A1
EP2826458A1 EP20130176867 EP13176867A EP2826458A1 EP 2826458 A1 EP2826458 A1 EP 2826458A1 EP 20130176867 EP20130176867 EP 20130176867 EP 13176867 A EP13176867 A EP 13176867A EP 2826458 A1 EP2826458 A1 EP 2826458A1
Authority
EP
European Patent Office
Prior art keywords
closure
vial container
vial
cap
penetrable portion
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.)
Withdrawn
Application number
EP20130176867
Other languages
German (de)
English (en)
Inventor
Theo Arnitz
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
F Hoffmann La Roche AG
Original Assignee
F Hoffmann La Roche AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by F Hoffmann La Roche AG filed Critical F Hoffmann La Roche AG
Priority to EP20130176867 priority Critical patent/EP2826458A1/fr
Publication of EP2826458A1 publication Critical patent/EP2826458A1/fr
Withdrawn legal-status Critical Current

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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
    • A61J1/1406—Septums, pierceable membranes
    • 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
    • B65D51/00—Closures not otherwise provided for
    • B65D51/002—Closures to be pierced by an extracting-device for the contents and fixed on the container by separate retaining means
    • 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
    • A61J1/1412—Containers with closing means, e.g. caps
    • A61J1/1425—Snap-fit type
    • 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
    • B65D2251/00—Details relating to container closures
    • B65D2251/20—Sealing means

Definitions

  • the present invention relates to closures for vials such as medical vials containing medicaments and serums.
  • vials such as medical vials containing medicaments and serums include a penetrable member extending across the open top of a vial container and being held thereon by an aluminum collar crimped to the neck portion of the vial container.
  • a hypodermic needle may be inserted through the penetrable member for removal of the contents therefrom.
  • the process of crimping the aluminum collar to the neck of the vial container is susceptible to accidents and damages. Such accidents and damages may cause complaints and production blackouts.
  • the reasons are, on the one hand side, that particles are generated during crimping, which contravenes the requirements of sterility, and, on the other hand side, the aluminum collar or the vial container may be damaged during crimping.
  • the penetrable member is not sterile and requires the user of the vial to disinfect the penetrable member before inserting the needle therethrough. Further, the collar may not be closed again after opening the vial.
  • US 2011/0000872 A1 describes a stopper device comprising a supporting cap and a container provided with such a cap.
  • US 2010/0224632 A1 describes a closure comprising a stopper made of elastomer and a cover for covering a neck of a container and the stopper.
  • the present invention provides a closure which may be used in a simple manner, provides advantages in view of sterility, decreases the manufacturing costs and reduces the number of used materials for closing the vial container as well as the number of elements to be handled.
  • the terms “have”, “comprise” or “include” or any arbitrary grammatical variations thereof are used in a non-exclusive way. Thus, these terms may both refer to a situation in which, besides the feature introduced by these terms, no further features are present in the entity described in this context and to a situation in which one or more further features are present.
  • the expressions “A has B”, “A comprises B” and “A includes B” may both refer to a situation in which, besides B, no other element is present in A (i.e. a situation in which a solely and exclusively consists of B) and to a situation in which, besides B, one or more further elements are present in entity A, such as element C, elements C and D or even further elements.
  • a closure for a vial comprising a vial container and a sealing comprises:
  • the body and the penetrable portion may be made of different materials.
  • the body and the penetrable portion may be made of different compounds.
  • the body may comprise an opening, wherein the penetrable portion may be disposed within the opening, wherein the cap may be moveable between a closed position in which the opening is closed and the penetrable portion protected by the cap and an open position in which the opening and the penetrable portion are exposed.
  • the cap may comprise a pin, wherein the pin may be disposed at the cap such that the pin contacts the penetrable portion, such as an outer surface thereof, in the closed position.
  • the cap may be adapted to reclose the opening and re-protect the penetrable portion after a displacement.
  • the closure may further comprise at least one guiding element disposed at the body to allow a fixation of the closure on the vial container without sealing the vial container.
  • the closure may be disposed on the vial container by means of the at least one guiding element without the sealing providing a tight connection between the vial container and the body.
  • the at least one guiding element allows to loosely dispose the closure on the vial container.
  • the cap may be hinged to the body.
  • the cap and the body may be integrally formed.
  • the body, the sealing and the penetrable portion may be integrally formed.
  • the body, the sealing, the penetrable portion, the holding element and the cap may be integrally formed.
  • the pin may comprise at least one germicide. The germicide may be adhered to a surface of the pin.
  • the germicide may be integrated into the pin.
  • the germicide may be doped into the pin.
  • the germicide may be silver iodide.
  • the holding element may be adapted to be deformed inwardly from the body.
  • the holding element may comprise at least one hook portion which is elastically deformable.
  • a vial according to the present invention may comprise:
  • the cap may be disposed such that the cap covers the penetrable portion.
  • the cap may comprise a pin, wherein the pin may be disposed at the cap such that the pin contacts the penetrable portion in a closed position of the cap.
  • the sealing may be disposed between the vial container and the body.
  • the sealing may be disc shaped.
  • the sealing may be an elastomeric stopper.
  • the closure may comprise the sealing and/or the penetrable portion.
  • the pin may comprise a germicide.
  • a method for closing a vial container with a closure according to the present invention comprises:
  • the method steps may be performed in the given order or in a different order. Further, two or more or even all of the method steps may be performed simultaneously and/or overlapping in time. Further, one, two or more or even all of the method steps may be performed repeatedly. The method may further comprise additional method steps.
  • the closure may be attached to the vial container after freeze drying the liquid.
  • the sealing may be disposed between the vial container and the body of the closure.
  • the holding element of the closure may comprise at least one hook portion which is elastically deformed so as to engage a surface of the vial container.
  • a method for manufacturing a closure according to the present invention comprises:
  • the method steps may be performed in the given order or in a different order. Further, two or more or even all of the method steps may be performed simultaneously and/or overlapping in time. Further, one, two or more or even all of the method steps may be performed repeatedly. The method may further comprise additional method steps.
  • the body and the penetrable portion may be made of different materials such as different compounds.
  • the body and the penetrable may be manufactured by means of sandwich injection molding.
  • different materials may be injection molded for forming the body and the penetrable portion.
  • the penetrable portion may be made of an elastomeric material.
  • the body may be made of plastics. Needless to say, the complete closure may be formed by means of injection molding.
  • vial as used herein relates to any kind of vessel or bottle which is adapted to store medication as liquids, powders or capsules. Such vials may also be called as a phial or flacon.
  • the vial basically comprises a vial container and a closure.
  • the vial container may be made of glass or plastics such as polypropylene.
  • the vials of the present invention may be used as sample vessels, for instance, in autosampler devices in analytical chromatography.
  • the vial may further comprise additional components such as a sealing which may be part of the closure.
  • a sealing which may be part of the closure.
  • the sealing may be integrally formed with the closure.
  • the sealing may be a separate constructional member.
  • the sealing may be connectable or connected to the closure.
  • the sealing is adapted to provide a gas and/or liquid tight connection between the vial container and the closure.
  • the sealing may be an elastomeric sealing or the like.
  • the penetrable portion may be adapted to allow a solid and/or liquid transfer from the vial container to an exterior thereof.
  • the penetrable portion may be an elastomeric penetrable member.
  • the penetrable portion may be penetrated by a needle or the like in order to remove the contents such as the liquid or solid from the vial container.
  • the needle may be a separate constructional member or may be part of an autosampler device such as an autosampler device in analytical chromatography.
  • closure as used herein relates to any element which is adapted to cover or seal the vial container.
  • the closure is one that completely closes the vial container.
  • the closure may be at least partially made of plastics.
  • the closure of the present invention basically comprises a body, a holding element, a penetrable portion and a cap.
  • holding element as used herein relates to any kind of element which is adapted to hold the closure permanently secure on the vial container.
  • the holding element may be adapted to be deformed inwardly from the closure.
  • the holding element may comprise at least one hook portion which is elastically deformable. This hook portion may interact with a portion of the vial container such as a neck portion similar to a snap-fit.
  • cap as used herein relates to any element which is adapted to protect the penetrable portion from external influences ad particularly from the entrance of germs, bacteria, microorganisms, contaminants or the like.
  • the cap may be flat, hemispherical-shaped or the like.
  • germ free as used herein relates to a state of the penetrable portion in which absolutely no or only very few germs are present on the penetrable portion at least in the period from manufacturing the vial until use of the vial. Accordingly, the "term germ” free comprises exact germ free and, if applicable, low-germ as far as the vial with such a low-germ penetrable portion may still be used in the intended chemical, biological, physical or medical field without any risk of adverse effects such as illness or contamination.
  • pin as used herein relates to any long body having a sharp, edged, rounded or flat tip.
  • the pin may be at least partially made of plastics.
  • the pin may be integrally formed with the closure such as a cap of the closure.
  • the pin may comprise at least one germicide.
  • the design of the pin allows to cover the whole surface of the opening in which the penetrable portion is arranged.
  • the term "germicide” as used herein relates to any agent that is adapted to kill germs, bacteria, microorganisms and the like, especially pathogenic microorganisms.
  • the germicide may be adhered to a surface of the pin.
  • the germicide may be sprayed onto the pin in a manner so as to remain thereon.
  • the germicide may be integrated into the pin.
  • the germicide may be doped into the pin.
  • the germicide may be silver iodide or the like.
  • compound as used herein relates to a mixture of different mono-material raw materials into which further filling materials, enhancing materials and/or additives are mixed. Thus, at least two substances are compounded to a homogenous mixture.
  • injection molding as used herein relates to a manufacturing process for producing parts by injecting material into a mold. Injection molding can be performed with a host of materials, including metals, glasses, elastomers, confections, and most commonly thermoplastic and thermosetting polymers. In the field of the present invention, plastic materials are used for injection molding.
  • the material for the to be formed part such as the body and the penetrable portion is fed into a heated barrel, mixed, and forced into a mold cavity corresponding to the desired shape of the body and the penetrable portion where it cools and hardens to the configuration of the cavity.
  • a basic idea of the present invention is to use a closure that provides germ free protection of the penetrable portion and that is easily as well as securely mountable to the vial container.
  • the closure of the present invention allows a secure handling for the user and is fraud resistant.
  • the body and the penetrable portion are integrally formed and the closure comprises a cap.
  • the cap covers at least the penetrable portion such that the same is protected in a germ free manner as described above.
  • the cap is adapted to re-cover the penetrable portion after a displacement.
  • the cap may be hinged to the body of the closure so as to be movable between a closed position, in which the penetrable portion is covered by the cap, and an open position, in which the penetrable portion is uncovered or exposed by the cap. In the open position, the penetrable portion is adapted to be penetrated by a needle or the like. If the cap is hinged to the body, the closure may be integrally formed so as to decrease the manufacturing costs.
  • FIG. 1 shows a perspective view of a vial 100 according to an embodiment of the present invention.
  • the vial 100 comprises a vial container 110.
  • the vial container 110 may be adapted to hold a liquid such as a medical liquid.
  • the vial container 110 comprises a neck portion 120 defining a container opening 130 through which the liquid may be filled into and removed from the vial container 110.
  • the vial container 110 further comprises a rim portion 140 arranged at the free end of the neck portion 120.
  • the rim portion 140 comprises an upper side 150 facing away from the neck portion 120 and a lower side 160 facing the neck portion 120.
  • the vial 100 further comprises a closure 170.
  • the closure 170 is at least partially made of plastics.
  • the closure 170 comprises a body 180, at least one holding element 190 adapted to hold the closure 170 permanently secure on the vial container 110, and a cap 200.
  • the body 180 defines an opening 210.
  • the body 180 comprises two flat protrusions 220 ( Figures 2 and 3 ) at an upper side 230 thereof.
  • the protrusions 220 are arranged parallel to one another so as to form a rectangular gap or recess 240 ( Figure 3 ) therebetween.
  • the opening 210 is defined within the recess 240.
  • the cap 200 is formed generally rectangular with a size adapted to the size of the recess 240. With other words, the cap 200 may be disposed within the recess 240 and two opposing side surfaces of the cap 200 contact two opposing side surfaces of the protrusions 220 but do not obstruct the cap 200.
  • the cap 200 is hinged to the body 180.
  • the cap 200 and the body 180 are integrally formed.
  • the cap 200 comprises a pin 250.
  • the pin 250 is arranged at a lower side 260 of the cap 200 facing the body 180.
  • the pin 250 comprises at least one germicide.
  • the germicide may be adhered to a surface of the pin 250. Alternatively or additionally, the germicide may be integrated into the pin 250.
  • the germicide is doped into the pin 250.
  • the germicide is silver iodide. Needless to say, the germicide may be any germicide adapted to be adhered to or integrated into the pin 250 such as tosylchloramide, ethanol and isopropan
  • the holding element 190 is adapted to be deformed inwardly from the body 180.
  • the holding element 190 comprises at least one hook portion 270 which is elastically deformable.
  • three to five holding elements 190 each comprising a hook portion 270 are present.
  • four holding elements 190 each comprising a hook portion 270 are disposed at the body 180 even though only one holding element 190 is shown in Figure 1 for simplification or illustration purposes.
  • the holding elements 190 are disposed around the circumference of the body 180 such as evenly spaced apart from one another along the circumference of the body 180.
  • the vial 100 further comprises a sealing 280 and a penetrable portion 290.
  • the closure 170 comprises the penetrable portion 290.
  • the closure 170 may further comprise the sealing 280.
  • the body 180 and the penetrable portion 290 are integrally formed.
  • the body 180, the sealing 280, the penetrable portion 290, the holding element 190 and the cap 200 may be integrally formed.
  • the sealing 280 may be a separate constructional member from the closure 170.
  • the sealing 280 is an elastomeric sealing.
  • the sealing 280 may be an elastomeric stopper.
  • the sealing 280 is ring-shaped.
  • the sealing 280 is disposed between the body 180 of the closure 170 and the vial container 110.
  • the sealing 280 is disposed on the rim portion 140 of the neck portion 120 such that sealing 280 is sandwiched between the vial container 110 and the body 180.
  • the holding element 190 is adapted to hold the closure 170 on the vial container 110 such that the sealing 280 is adapted to provide a tight connection between the vial container 110 and the body 180.
  • the body 180 of the closure 170 is pressed to a certain degree onto the rim portion of the vial container 110 by the holding element 190.
  • the penetrable portion 290 is an elastomeric penetrable portion.
  • the body 180 and the penetrable portion 290 are made of different materials such as different compounds.
  • the penetrable portion 290 is disc-shaped.
  • the penetrable portion 290 is disposed within the opening 210 of the body 180.
  • the penetrable portion 290 is adapted to be penetrated by a needle or the like in order to be adapted to allow a liquid transfer as will be explained in more detail below.
  • the cap 200 is adapted to provide a germ free protection of the penetrable portion 290 as will be explained in more detail below.
  • the cap 200 is moveable between an open position and a closed position as will be explained in more detail below.
  • Figure 2 shows a perspective view of the closure 170 in a closed position.
  • the opening 210 is closed and the penetrable portion 290 protected or covered by the cap 200.
  • the pin 250 is disposed at the cap 200 such that the pin 250 contacts the penetrable portion 290 in the closed position.
  • the germicide of the pin 250 comes into contact with the penetrable portion 290 so as to disinfect the same.
  • the pin 250 may exert a pressing force onto the penetrable portion 290 in order to ensure that the germicide comes into contact with the penetrable portion 290.
  • the body 180 may comprise a depression 300 or the like allowing a user of the vial 100 to engage or grasp the lower side 260 of the cap 200 with his or her finger in order to move the same from the closed position into the open position.
  • Figure 3 shows a perspective view of the closure 170 in an open position.
  • the opening 210 and the penetrable portion 290 are exposed.
  • the penetrable portion 290 is ready to be penetrated by a needle or the like.
  • the cap 200 is hinged to the body 180, the cap 200 is adapted to reclose the opening 210 and re-protect or re-cover the penetrable portion 290 after a displacement.
  • the closure 170 may be manufactured as will be explained below.
  • the body 180 is formed of a first material.
  • the penetrable portion 290 is formed of a second material different from the first material.
  • the body 180 and the penetrable portion 290 may be formed of the materials as specified above.
  • the body 180 may be formed of plastics and the penetrable portion 290 may be formed of an elastomeric material different from the plastics.
  • the body 180 and the penetrable portion 290 are integrally formed.
  • the body 180 and the penetrable portion 290 may be manufactured by means of injection molding such as sandwich injection molding.
  • the different materials may be injection molded for forming the body 180 and the penetrable portion 290.
  • the at least one holding element 190 and the cap 200 are formed as well.
  • the complete closure 170 may be formed by means of injection molding.
  • the vial container 110 for holding a liquid is provided and filled with a liquid.
  • the sealing 280 is disposed so as to close vial container 110.
  • the sealing 280 is disposed onto the rim portion 140 of the vial container 110.
  • the closure 170 which is preferably integrally formed with the sealing 280, is loosely disposed on the rim portion 140 of the vial container 110.
  • the sealing 280 is disposed between the vial container 110 and the body 180 of the closure 170.
  • the penetrable portion 290 is also arranged on the vial container 110 such that penetrable portion 290 is partially disposed within the opening 130 of the neck portion 120.
  • the pin 250 of the cap 200 is treated with a germicide in the above explained manner.
  • the cap 200 is moved into the closed position, in which the pin 250 contacts the penetrable portion 290.
  • the penetrable portion 290 is disinfected as the germicide of the pin 250 comes into contact with the penetrable portion 290.
  • the pin 250 and the penetrable portion 290 may already be disinfected when the closure 170 is loosely disposed on the vial container 110.
  • the pin 290 may be treated with the germicide by a manufacturer of the closure 170 and supplied to a customer in a disinfected state.
  • the closure 170 is attached to the vial container 110 such that the holding element 190 is partially deformed such that the closure 170 is permanently secured to the vial container 110.
  • the closure 170 is moved or pushed towards the vial container 110.
  • the holding element 190 is moved over the rim portion 140 of the vial container 110.
  • the hook portion 270 is elastically deformed outward from the body 180 when being moved over the rim portion 140 of the vial container 110. If the hook portion 270 is completely moved over the rim portion 140 of the vial container 110, the hook portion 270 is deformed inward towards the body 180 and engages a surface of the vial container 110, which is the lower side 160 of the rim portion 140.
  • the vial container 110 may be closed and sealed in a single step in that the closure is loosely disposed on the vial container 110 and pushed towards the vial container 110.
  • a vial container closed by a conventional closure needs at least two steps to be closed. First, a stopper constituting a sealing and a penetrable portion is put or disposed on the vial container. Then, in a second process step, the crimping cap is placed on top of the stopper and the vial will be crimped such that the engagement portion engages the rim portion and holds the stopper permanently secure on the vial container. These two process steps are necessary for closing the vial container because the stopper and the crimp cap are two separate constructional members.
  • Figure 4 shows a cross-sectional view of a vial 100 according to another embodiment of the present invention.
  • the closure 170 comprises at least one guiding element 310 disposed at the body 180.
  • the closure 170 comprises at least one guiding element 310 disposed at the body 180.
  • three to five guiding elements 310 are present.
  • three guiding elements 310 are disposed at the body 180. More particularly, the guiding elements 310 are disposed around the circumference of the body 180 such as evenly spaced apart from one another along the circumference of the body 180.
  • Figure 5 shows a cross-sectional view of the vial 100 of Figure 4 after freeze-drying with the closure 170 after being mounted to the vial container 110.
  • the guiding element 310 allows a fixation of the closure 170 on the vial container 110 without sealing of the vial container 110.
  • the hook portion 270 engages the lower side 160 of the rim portion 140 such that the closure 170 is permanently secured to the neck portion 120.
  • the guiding element 310 completely extends through the opening 130 of the vial container 110.
  • the liquid within the vial container 110 is freeze dried.
  • the closure 170 is attached to the vial container 110 in the manner explained above, i.e. the closure 170 is moved or pushed towards the vial container 110 in order to permanently secure the closure 170 to the vial container 110.

Landscapes

  • 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)
  • Closures For Containers (AREA)
EP20130176867 2013-07-17 2013-07-17 Capuchon pour ampoule Withdrawn EP2826458A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP20130176867 EP2826458A1 (fr) 2013-07-17 2013-07-17 Capuchon pour ampoule

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP20130176867 EP2826458A1 (fr) 2013-07-17 2013-07-17 Capuchon pour ampoule

Publications (1)

Publication Number Publication Date
EP2826458A1 true EP2826458A1 (fr) 2015-01-21

Family

ID=48793960

Family Applications (1)

Application Number Title Priority Date Filing Date
EP20130176867 Withdrawn EP2826458A1 (fr) 2013-07-17 2013-07-17 Capuchon pour ampoule

Country Status (1)

Country Link
EP (1) EP2826458A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020154570A1 (fr) * 2019-01-25 2020-07-30 West Pharmaceutical Services, Inc. Mesure non destructive, en temps réel, d'intégrité de fermeture de récipient

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5088612A (en) 1991-06-10 1992-02-18 Comar, Inc. Vial cap
EP0769456A2 (fr) * 1995-10-18 1997-04-23 Daikyo Seiko, Ltd. Capuchon en plastique et son procédé de fabrication
WO1999053886A1 (fr) 1998-04-20 1999-10-28 Becton Dickinson And Company Fermeture en plastique pour flacons et autres recipients medicaux
EP1094012A2 (fr) 1999-10-20 2001-04-25 Becton, Dickinson and Company Fermeture en plastique pour flacons et autres recipients medicaux
EP1412261A1 (fr) * 2001-08-03 2004-04-28 Helvoet Pharma Belgium N.V. Bouchon de fermeture destine a des flacons de perfusion ou de transfusion
US20100224632A1 (en) 2005-11-30 2010-09-09 Antoine Aneas Plug Device for a Container and Container Provided With One Such Device
US20110000872A1 (en) 2008-02-11 2011-01-06 Biocorp Recherche Et Devloppment Stopper device comprising a supporting cap, and container provided with such a device

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5088612A (en) 1991-06-10 1992-02-18 Comar, Inc. Vial cap
EP0769456A2 (fr) * 1995-10-18 1997-04-23 Daikyo Seiko, Ltd. Capuchon en plastique et son procédé de fabrication
WO1999053886A1 (fr) 1998-04-20 1999-10-28 Becton Dickinson And Company Fermeture en plastique pour flacons et autres recipients medicaux
EP1094012A2 (fr) 1999-10-20 2001-04-25 Becton, Dickinson and Company Fermeture en plastique pour flacons et autres recipients medicaux
EP1412261A1 (fr) * 2001-08-03 2004-04-28 Helvoet Pharma Belgium N.V. Bouchon de fermeture destine a des flacons de perfusion ou de transfusion
US20100224632A1 (en) 2005-11-30 2010-09-09 Antoine Aneas Plug Device for a Container and Container Provided With One Such Device
US20110000872A1 (en) 2008-02-11 2011-01-06 Biocorp Recherche Et Devloppment Stopper device comprising a supporting cap, and container provided with such a device

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2020154570A1 (fr) * 2019-01-25 2020-07-30 West Pharmaceutical Services, Inc. Mesure non destructive, en temps réel, d'intégrité de fermeture de récipient
US11982593B2 (en) 2019-01-25 2024-05-14 West Pharmaceutical Services, Inc. Real-time, non-destructive Container Closure Integrity measurement

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