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Vented Vial Adapter

by West Pharma. Services IL, Ltd. 3 variants

Ref 8073039

Expiring European Union. Also listed in GUDID (US).

CE MDR

Valid until

1 Aug 2027

CE MDR certificate

FDA recalls

None found

in data synced 22 Oct 2026

Documents

1 certificate

Certifier DEKRA Certification B.V.

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number3902869CE01 Date6 Jul 2026IssuedStatusExpiring expires 1 Aug 2027
United StatesGUDID listing GUDID Number07290108241129 UDI-DI Date8 Apr 2018ListedStatusListed GUDID: in commercial distribution

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 3902869CE01 Expiring Amended Expires in 274 days

    Quality management system EU MDR

    Certifier
    DEKRA Certification B.V. 0344
    Issued
    6 Jul 2026
    Expires
    1 Aug 2027
    Reason
    Other

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Expiring
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Vented Vial Adapter EUDAMED
Vented Vial Adapter 20mm GUDID
Generic Name
Medication transfer needle, filtering/vented
Device Name
Vented Vial Adapter™
Model / Reference
8073039
Primary DI / UDI-DI
07290108241129
Basic UDI-DI
729010824VVAL7
510(k) Number
FDA Product Code
LHI
EMDN Code
A0704 Systems for reconstitution and administration of pharmaceuticals
GMDN Term
Medication transfer needle, filtering/vented
Device Class
Class I EUDAMED
Class II GUDID
Regulation Number
880.5440
EU market of registration
Austria
GUDID distribution status
In Commercial Distribution
Sterilization Method
Radiation Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class I
GUDID
Class II

Manufacturer details

EUDAMED SRN
IL-MF-000008572
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Other devices from West Pharma. Services IL, Ltd.

See all devices from West Pharma. Services IL, Ltd. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (19)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No