US20090171296A1 - Needle assembly for a prefilled syringe system - Google Patents

Needle assembly for a prefilled syringe system Download PDF

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Publication number
US20090171296A1
US20090171296A1 US12/064,252 US6425206A US2009171296A1 US 20090171296 A1 US20090171296 A1 US 20090171296A1 US 6425206 A US6425206 A US 6425206A US 2009171296 A1 US2009171296 A1 US 2009171296A1
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US
United States
Prior art keywords
needle
sheath
seal
set forth
closure element
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US12/064,252
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English (en)
Inventor
Arthur Fabian
Stefan Beyeler
Andreas Eberle
Jasminka Kovac
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.)
Cilag GmbH International
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Assigned to ETHICON ENDO-SURGERY, INC. reassignment ETHICON ENDO-SURGERY, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: EBERLE, ANDREAS, BEYELER, STEFAN, FABIAN, ARTHUR, KOVAC, JASMINKA
Publication of US20090171296A1 publication Critical patent/US20090171296A1/en
Assigned to CILAG GMBH INTERNATIONAL reassignment CILAG GMBH INTERNATIONAL ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: ETHICON ENDO-SURGERY, INC.
Abandoned legal-status Critical Current

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm rests
    • A61M5/178—Syringes
    • A61M5/31—Details
    • A61M5/32—Needles; Details of needles pertaining to their connection with syringe or hub; Accessories for bringing the needle into, or holding the needle on, the body; Devices for protection of needles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm rests
    • A61M5/178—Syringes
    • A61M5/31—Details
    • A61M5/32—Needles; Details of needles pertaining to their connection with syringe or hub; Accessories for bringing the needle into, or holding the needle on, the body; Devices for protection of needles
    • A61M5/3202—Devices for protection of the needle before use, e.g. caps
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm rests
    • A61M5/178—Syringes
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm rests
    • A61M5/178—Syringes
    • A61M5/31—Details
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm rests
    • A61M5/178—Syringes
    • A61M5/31—Details
    • A61M5/32—Needles; Details of needles pertaining to their connection with syringe or hub; Accessories for bringing the needle into, or holding the needle on, the body; Devices for protection of needles
    • A61M5/34—Constructions for connecting the needle, e.g. to syringe nozzle or needle hub
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm rests
    • A61M5/178—Syringes
    • A61M5/31—Details
    • A61M2005/3103—Leak prevention means for distal end of syringes, i.e. syringe end for mounting a needle
    • A61M2005/3107—Leak prevention means for distal end of syringes, i.e. syringe end for mounting a needle for needles
    • A61M2005/3109—Caps sealing the needle bore by use of, e.g. air-hardening adhesive, elastomer or epoxy resin
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T29/00—Metal working
    • Y10T29/49—Method of mechanical manufacture
    • Y10T29/49826—Assembling or joining
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T29/00—Metal working
    • Y10T29/49—Method of mechanical manufacture
    • Y10T29/49826—Assembling or joining
    • Y10T29/49904—Assembling a subassembly, then assembling with a second subassembly

Definitions

  • the invention relates to a needle assembly for a prefilled injection syringe, especially but not exclusively of the type that is coated on the inside by means of baked siliconizing and sterilized in a heating tunnel at a temperature of up to 350° C., comprising: a needle holder with a needle secured thereto, the needle being securable to a syringe barrel of the injection syringe, a needle shielding sheath, the distal end of which fixedly sterile seals the needle holder, but releasably connected thereto and shieldingly surrounding the needle, a needle seal for mounting the needle tip arranged at least in part in the proximal end of the needle shielding sheath closed off by a closure element.
  • a system is described in WO 94/22511 wherein a preassembled needle assembly with a bonded needle, needle seal as well as needle shield can be assembled e.g. in an aseptic environment to a siliconized and sterilized syringe barrel.
  • a snap-action connector between end cap and cannula shield constitutes no microbiological shield for the needle in conjunction with the end contact face. Rendering the needle surface sterile is achieved by snap-action connection of cap and cannula shield, compressing the cannula shield of cap and cannula shield in sealing the resulting cavity surrounding the needle surface.
  • Such a snap-action connector can be engineered releasable and thus represents a certain risk as regards rendering the needle surface sterile, as may be the case, e.g. when having become loose unnoticed during shipment or handling.
  • EP 0 240 787 describes a system for shielding parenteral needles involving a bonded needle, a needle seal and needle shield. There is no mention of how rendering the needle sterile is assured. Connecting the housing and needle hub is said to be achieved by axially staggered ribs which although achieving a certain secure location of the housing, fail to assure the necessary microbiological or sterile seal.
  • the invention is thus based on the object of improving a generic needle holder so that a sterile seal of the needle holder is assured in cost-saving production thereof so that maintaining the complete needle sterile in the time between sterilizing the needle assembly and the moment it is put to use is now reliably assured.
  • the invention is characterized by the closure connection between the closure element and the needle shielding sheath being configured as a non-releasable and sterile barrier produced by means of a bonding or welding technique.
  • the sterile barrier is preferably a closure connection produced by ultrasonic or laser welding.
  • non-toxic, acrylic-based adhesives for curing by means of UV light or at room temperature, such as e.g. adhesive type LOCTITE® 3011, Henkel Loctite Kunststoff GmbH, 81925 Kunststoff, epoxy resin by Barton Solvents Inc., Desmoines, USA.
  • closure element and the needle shielding sheath preferably of an amorphous thermoplastic, such as polycarbonate or polystyrene or a partly crystalline thermoplastic, such as polypropylene or polythene produces good results.
  • an amorphous thermoplastic such as polycarbonate or polystyrene or a partly crystalline thermoplastic, such as polypropylene or polythene produces good results.
  • closure element is a cap with a cylindrical sleeve
  • needle shielding sheath is a tubular member, the proximal end of which is provided with a ring flange, the distal rim of the cap shell connecting the ring flange of the needle shielding sheath in forming a sterile barrier.
  • the ring flange of the needle shielding sheath may be provided at the outer edge of its proximal side to advantage with an annular face for securing the bottom rim of the cap shell.
  • the distal rim of the cap shell comprises an interlocking profile
  • the annular securing face of the ring flange of the needle shielding sheath comprises a receiving profile shaped to comply with the interlocking profile of the cap shell and in which the interlocking profile is inserted for positive and/or non-positive interlocking.
  • the interlocking profile at the distal rim of the cap shell may also be shaped as an energy director where an ultrasonic weld with the needle shielding sheath is feasible.
  • Another aspect of the invention is characterized by a supporting collar jutting forwards from the proximal side of the ring flange of the needle shielding sheath radially within the outer annular securing face for the closure element.
  • the needle seal is provided at its proximal end preferably with a flange-type extension which is supported by the supporting collar of the needle shielding sheath.
  • the distal side of the cover contacts the proximal end of the needle seal.
  • the proximal side of the flange-type extension of the needle seal is provided with a ring collar contacting the distal side of the head side of the closure element.
  • the supporting flange of the needle shielding sheath and the supporting collar may each comprise at the supporting flange of the needle shielding sheath a cylindrical centre hole whose bore corresponds to the bore of the cylindrical inner surface area of the needle shielding sheath.
  • This aspect can be modified in a second embodiment such that the inner surface area of the supporting collar of the needle shielding sheath is flared conically proximally and that the flange-type extension of the needle seal has a circumferential surface area which at least over a portion of its distal end matches the shape of the conical inner surface area of the supporting collar and is supported by this conical portion at the inner surface area of the supporting collar.
  • the distal end of the needle seal receiving the needle tip contains a central opening for the needle.
  • a longitudinal portion of the needle seal arranged distally of the flange-type extension extends by the supporting collar into the proximal end of the needle shielding sheath.
  • the diameter of this distal longitudinal portion may be smaller or equal to the diameter of the inner space of the needle shielding sheath.
  • the needle shielding sheath is integrally connected at its distal end by a designed frangible connection to a proximal portion of the needle holder in thus making it possible to totally expose the needle ready for use after having destroyed just a single designed frangible connection.
  • the needle should be preferably made of a stainless steel and either fixedly bonded in the needle holder coaxially to the barrel of the syringe or fixedly connected to the needle holder by a plastics potting.
  • the needle holder itself may be made preferably of a thermoplastic, such as polycarbonate, polypropylene or polyamide.
  • the needle assembly in accordance with the invention is excellently tamperproof on opening the prefilled injection syringe due to the sterile barrier between closure element and needle shielding sheath whilst assuring simple production and component assembly in producing the needle assembly as well as simple assembly of the needle assembly to a siliconized syringe barrel.
  • the preferred method of manufacturing the needle assembly includes securing a needle to a needle holder that is adapted to be secured to a syringe barrel of the injection syringe, releasably connecting the distal end of a needle sheath to the needle holder to form a sterile seal, and to surround and shield the needle, locating a needle seal on the needle tip and at least in part in the proximal end of the needle sheath, and closing off the proximal end of the needle seal with a closure element by forming a closure connection between the closure element and the needle sheath, configured as a non-releasable and sterile barrier, by means of bonding or welding.
  • a first subassembly of the needle seal, closure element and needle sheath is formed, in which the needle seal is arranged at least in part in the proximal end of the needle sheath and the closure element closes off the proximal end of the needle seal, a second subassembly is formed by securing the needle to the needle holder, and the first and second subassemblies are offered up to one another so that the needle sheath releasably connects at its distal end to the needle holder to form a sterile seal, and surrounds and shields the needle, and the needle seal locates on the needle tip.
  • a first subassembly is formed by securing the needle to the needle holder
  • a second subassembly is formed by inserting the first subassembly into the needle sheath
  • a third subassembly is formed by mounting the needle seal onto needle tip and needle sheath of the second subassembly
  • the needle assembly is completed by forming the closure connection between the closure element and the needle sheath of the third subassembly.
  • FIG. 1 is a longitudinal centreline section through a first embodiment of a needle assembly in accordance with the invention as it leaves production;
  • FIG. 2 is a longitudinal centreline section through a second embodiment of the invention as it leaves production
  • FIG. 3 is a longitudinal centreline section, on a magnified scale, through a cover with an energy director prior to assembly, for a needle shielding sheath of the needle assembly as shown in FIGS. 1 or 2 ;
  • FIG. 4 is a longitudinal. centreline section, on a magnified scale, through a second modified embodiment of a cover for needle assembly;
  • FIG. 5 is a longitudinal centreline section, on a magnified scale, through a needle seal of the needle assembly as shown in FIG. 1 ;
  • FIG. 6 is a longitudinal centreline section, on a magnified scale, through a needle seal of the needle assembly as shown in FIG. 2 .
  • FIG. 1 there is illustrated a needle assembly for a prefilled injection syringe made of glass or plastics, known as such and thus not shown, coated on the inside by means of baked siliconizing and sterilized in a heating tunnel at a temperature of up to 350° C.
  • the needle assembly 10 is composed of a needle holder 12 and secured thereto a needle 14 , a needle shielding sheath 16 , a needle seal 18 and a closure element 20 .
  • the needle holder 12 is tapered, featuring at its distal end a conical opening 22 provided with an annular groove 24 so that the needle holder 12 can be fitted to a moulded barrel with an annular bead of a prefilled injection syringe known as such and thus not shown, and secured thereto by snap-action connection.
  • the conical opening 22 translates at its proximal end into a cylindrical bore 26 in which the needle 14 is coaxially secured by its distal end with the aid of an adhesive 28 .
  • Useful adhesives are non-toxic, acrylic-based adhesives for curing by means of UV light or at room temperature, such as e.g. adhesive type LOCTITE® 3011, Henkel Loctite Kunststoff GmbH, 81925 Kunststoff, epoxy resin by Barton Solvents Inc., Desmoines, USA.
  • the needle 14 may also be secured by sleeve moulding it in the needle holder, whereby the same plastics material can be used for sleeve moulding the needle holder in an injection moulding technique as serving for production of the needle holder.
  • the needle 14 can be configured differing in length and is preferably made of a stainless steel of the type AISI 314 and is a cannula, the coaxially bore of which is exposed at the distal end.
  • a proximal end of the needle holder 12 is an annular face 30 surrounding the bonded needle 14 .
  • the needle holder 12 is preferably made of a thermoplastic such as e.g. polycarbonate, polypropylene or polyamide.
  • the needle shielding sheath 16 mainly comprises a tubular longitudinal portion 32 , the distal end of which is a secure and sterile seal connecting the outer edge of the annular face 30 of the needle shielding sheath 16 by a circumferential designed frangible connection 52 , but which can be released manually by exerting a fracturing force.
  • the needle shielding sheath 16 extends coaxially to the needle holder 12 in surrounding the needle 14 with a full length consistent radial spacing.
  • the outer diameter of the needle shielding sheath 16 is dimensioned only slightly larger than the diameter of the annular face 30 of the needle holder 12 .
  • the needle shielding sheath 16 extends by its tubular longitudinal portion 32 beyond the tip (not shown in FIG. 1 ) of the needle, the proximal end of the tubular longitudinal portion 32 featuring a ring flange 34 surrounding an opening, the diameter of which roughly corresponds to the inner diameter of the needle shielding sheath 16 .
  • the ring flange 34 extends outwards beyond the cylindrical outer side of the needle shielding sheath 16 .
  • the proximal end of the ring flange 34 features at its outer edge an annular securing face 36 , an annular supporting collar 38 being arranged within this annular securing face 36 .
  • the inner diameter of this supporting collar 38 roughly corresponds to that of the needle shielding sheath 16 and ring flange 34 respectively.
  • the needle shielding sheath 16 is preferably made of a partly crystalline thermoplastic, such as e.g. polypropylene or polythene.
  • the needle seal 18 is made of an elastomeric material, such as pharmaceutical rubber or a thermoplastic elastomer, and serves to shieldingly receive a proximal end of the needle 14 comprising a bevelled needle tip, and which is arranged at least in part in the proximal end of the needle shielding sheath 16 .
  • the needle seal 18 comprises a moulding featuring a conical distal end 40 containing a centering opening 42 for the needle tip in extending over roughly half the length of the needle seal 18 .
  • the conical distal end 40 then translates into a short cylindrical longitudinal 10 portion 44 contacting a cylindrical inner surface area 46 of the supporting collar 38 of the needle shielding sheath 16 .
  • the needle seal 18 is provided with a flange-type extension 48 supporting the needle seal 18 at the supporting collar 38 of the needle shielding sheath 16 .
  • a proximal end of the needle seal 18 is formed by an annular collar 50 protruding from an outer edge of the proximal end of the flange-type extension 48 of the needle seal 18 .
  • FIG. 5 there is illustrated a modified embodiment of the needle seal 18 in which merely a conical longitudinal portion 40 and a cylindrical longitudinal portion 44 located therebefore are dimensioned roughly the same in length.
  • the annular collar 50 has a triangular cross-section, the apex of which is proximal.
  • the proximal end of the needle assembly 10 comprises the closure element 20 closing off the needle shielding sheath 16 , this closure connection between the closure element 20 and needle shielding sheath 16 being configured as a sterile barrier 54 .
  • the closure element 20 is a cap 56 with a header plate 58 , from the outer rim of which a cylindrical shell 60 extends distally.
  • a distal rim 62 of the cylindrical shell 60 is connected to the securing face 36 of the ring flange 34 of the needle shielding sheath 16 in forming the sterile barrier 54 .
  • the closure element 20 clasps the portion of the needle seal 18 located before the supporting collar 38 as well as the supporting collar 38 .
  • the sterile barrier 54 between the closure element 20 and the needle shielding sheath 16 comprises particularly to advantage a bonded or welded connection.
  • non-toxic acrylic-based adhesives for curing by means of UV light or at room temperature, such as e.g. adhesive type LOCTITE® 3011, Henkel Loctite Kunststoff GmbH, 81925 Kunststoff, epoxy resin by Barton Solvents Inc., Desmoines, USA.
  • the closure element 20 is equipped at the distal rim 62 of its cap shell 60 preferably with an energy director 64 tapered distally into a triangular cross-section for faster, more effective welding of the distal rim 62 of the cap shell 60 to the securing face 36 at the outer edge of the ring flange 34 of the needle shielding sheath 16 .
  • FIG. 4 there is illustrated a cap 66 as a closure element 20 , the cylindrical shell of which comprises a distal free end having a smooth annular surface area 68 extending perpendicular to the longitudinal centreline of the closure element 20 .
  • This embodiment is provided to close off the needle shielding sheath 16 by a bonded connection forming the sterile barrier 54 .
  • closure element 20 of an amorphous thermoplastic, such as polycarbonate or polystyrene or a partly crystalline thermoplastic, such as polypropylene or polythene.
  • amorphous thermoplastic such as polycarbonate or polystyrene
  • a partly crystalline thermoplastic such as polypropylene or polythene.
  • FIG. 1 again there is illustrated how the header plate 58 of the cap-type closure element 20 contacts a proximal end of the needle seal 18 by its distal side 70 ( FIG. 3 ).
  • the closure element 20 merely contacts the elastomeric annular collar 50 of the needle seal 18 in compressing it in part, so that the needle seal 18 with its flange-type extension 48 is pressed against the supporting collar 38 of the needle shielding sheath 16 when the needle shielding sheath 16 is closed off sterile by the closure element 20 .
  • FIG. 2 there is illustrated the needle assembly 210 in a second embodiment in accordance with the invention in which like or similar elements of the second embodiment are identified by like reference numerals of the first embodiment but prefixed by 2.
  • This needle assembly 210 differs from that of the first embodiment substantially in that the inner surface area of a supporting collar 238 of the needle shielding sheath 216 is flared conically proximally.
  • a proximal flange-type extension 248 of the needle seal 218 comprises a circumferential surface area adapted at least in a partial portion of its distal end to the shape of the conical inner surface area 246 of the supporting collar 238 in being supported by this conical partial portion 246 on the conical inner surface area 246 of the supporting collar 238 .
  • a portion 240 of the needle seal 218 extending distally of the flange-type extension 248 is formed cylindrical in interlocking the supporting collar 238 as well as the proximal end of the needle shielding sheath 216 in creating a free, annular space 251 .
  • the needle seal 218 in this case too is made of a pharmaceutical rubber or thermoplastic elastomer.
  • Missing furthermore from this second embodiment at the needle seal 218 is an annular collar protruding from the flange-type extension distally in the direction of the distal side of the header plate 258 of the closure element 220 , resulting in the proximal side of the flange-type extension of the needle seal 218 directly contacting the distal side 270 of the header plate 258 of the closure element 220 .
  • the elastomeric material of the needle seal 218 is, however, in this second embodiment too, compressed by the closure element 220 when it is fixedly and non-releasable connected to the needle shielding sheath 216 to form a sterile barrier 254 with the needle shielding sheath 216 .
  • the two main procedures in assembling the cap-type closure element and the needle shielding sheath are as follows:
  • jointing and mounting method securing the closure element on the needle shield sheath by means of welding or bonding and, if applicable, follow-on steps such as e.g. curing the adhesive in producing the sterile barrier;
  • the needle assembly in accordance with the invention ensures the needle remaining sterile during storage of the prefilled injection syringe in thus rendering it safely tamperproof.
  • the needle assembly is simple to fit to a siliconized and sterilized syringe barrel on a mass production scale. All of the various component parts are simple to manufacture and assemble.

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  • Health & Medical Sciences (AREA)
  • Vascular Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Anesthesiology (AREA)
  • Biomedical Technology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Hematology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Infusion, Injection, And Reservoir Apparatuses (AREA)
US12/064,252 2005-08-30 2006-08-03 Needle assembly for a prefilled syringe system Abandoned US20090171296A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP05255298A EP1759729B1 (de) 2005-08-30 2005-08-30 Nadelvorrichtung für eine vorgefüllte Spritze
EP05255298.1 2005-08-30
PCT/IB2006/002792 WO2007026248A2 (en) 2005-08-30 2006-08-03 Needle assembly for a prefilled syringe system

Publications (1)

Publication Number Publication Date
US20090171296A1 true US20090171296A1 (en) 2009-07-02

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US12/064,252 Abandoned US20090171296A1 (en) 2005-08-30 2006-08-03 Needle assembly for a prefilled syringe system
US13/601,024 Active US9358346B2 (en) 2005-08-30 2012-08-31 Needle assembly for a prefilled syringe system

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Application Number Title Priority Date Filing Date
US13/601,024 Active US9358346B2 (en) 2005-08-30 2012-08-31 Needle assembly for a prefilled syringe system

Country Status (22)

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US (2) US20090171296A1 (de)
EP (1) EP1759729B1 (de)
JP (1) JP5550830B2 (de)
KR (1) KR101355875B1 (de)
CN (1) CN101277730B (de)
AT (1) ATE452670T1 (de)
AU (1) AU2006286227C1 (de)
BR (1) BRPI0616997B8 (de)
CA (1) CA2619543C (de)
DE (1) DE602005018480D1 (de)
DK (1) DK1759729T3 (de)
EA (1) EA013722B1 (de)
ES (1) ES2340936T3 (de)
IL (1) IL189608A (de)
MX (1) MX2008002728A (de)
NO (1) NO341297B1 (de)
NZ (1) NZ566080A (de)
PL (1) PL1759729T3 (de)
PT (1) PT1759729E (de)
UA (1) UA91232C2 (de)
WO (1) WO2007026248A2 (de)
ZA (1) ZA200802772B (de)

Cited By (2)

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Publication number Priority date Publication date Assignee Title
WO2018092138A1 (en) * 2016-11-17 2018-05-24 Syrinjector Ltd. Online, real-time mass vaccination and data collection system
US20210015708A1 (en) * 2018-03-28 2021-01-21 Cmc-Pharma Co., Ltd Two-component-mixing prefilled syringe kit

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FR3002738B1 (fr) * 2013-03-01 2020-11-20 Societe De Transf Des Elastomeres A Usages Medicaux Et Industriels Dispositif de protection d'aiguille.
FR3002739B1 (fr) 2013-03-01 2016-01-08 Transformation Des Elastomeres A Usages Medicaux Et Ind Soc D Dispositif de protection d'aiguille.
FR3002740B1 (fr) 2013-03-01 2016-01-08 Transformation Des Elastomeres A Usages Medicaux Et Ind Soc D Dispositif de protection d'aiguille.
GB2515038A (en) 2013-06-11 2014-12-17 Cilag Gmbh Int Injection device
GB2515039B (en) 2013-06-11 2015-05-27 Cilag Gmbh Int Injection Device
GB2515032A (en) 2013-06-11 2014-12-17 Cilag Gmbh Int Guide for an injection device
GB2517896B (en) 2013-06-11 2015-07-08 Cilag Gmbh Int Injection device
EP2862587A1 (de) 2013-10-15 2015-04-22 Becton Dickinson France Spitzenkappenanordnung zum Verschließen eines Injektionssystems
WO2015081337A2 (en) * 2013-12-01 2015-06-04 Becton, Dickinson And Company Medicament device
DE102016108870A1 (de) * 2016-05-13 2017-11-16 Gerresheimer Regensburg Gmbh Stechmittelschutzvorrichtung für eine Spritze
US10702652B2 (en) * 2016-11-15 2020-07-07 Adam Teach Injection device
EP3750580B1 (de) * 2019-06-13 2025-12-24 SCHOTT Pharma Schweiz AG Mit einem fluid vorfüllbarer oder vorgefüllter behälter sowie kanülenbaugruppe und verschlusssystem für einen mit einem fluid vorfüllbaren oder vorgefüllten behälter
CN114505508B (zh) * 2022-03-07 2023-06-02 深圳己道科技有限公司 内冷超声波刀柄

Citations (99)

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