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Vial Adapter 8070013

by West Pharma. Services Il, . Ltd

Ref 8070013

Vial Adapter 8070013 is a device classified as Class I in the EU and Class II in the US made by West Pharma. Services Il, . Ltd, registered in EUDAMED on 1 Jul 2026 (Basic UDI-DI B-07290108240566), cleared under FDA 510(k) K001293 on 5 May 2000 and listed in FDA GUDID since 19 Mar 2017 (UDI-DI 07290108240566), active as of 25 Oct 2026.

Active European Union and United States. Also listed in GUDID (US).

CE MDD 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None found

in data synced 25 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K001293

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-07290108240566 Basic UDI-DI 07290108240566UDI-DIDate1 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number07290108240566 UDI-DI Date19 Mar 2017ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Special NumberK001293 Date5 May 2000DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI B-07290108240566 registered 1 Jul 2026 Active
  • FDA 510(k) K001293 decided 5 May 2000 Active
  • FDA GUDID UDI-DI 07290108240566 listed 19 Mar 2017 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K001293
  2. Listed FDA GUDID 07290108240566
  3. Registered EUDAMED B-07290108240566

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Trade name
Vial Adapter
Generic name
Vial/bottle adaptor, non-hermetic
Model / reference
8070013
Primary DI / UDI-DI
07290108240566
Basic UDI-DI
B-07290108240566
510(k) Number
FDA product code
LHI
EMDN code
A0704 Systems for reconstitution and administration of pharmaceuticals
GMDN term
Vial/bottle adaptor, non-hermetic
Device class
Class I EUDAMED
Class II GUDID
Regulation number
880.5440
EU registration type
Legacy device (under a directive)
EU market of registration
Austria
GUDID distribution status
In Commercial Distribution
Sterilisation method
Radiation Sterilization

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Device classEUDAMED
Class I
GUDID
Class II
Sterilise before useEUDAMED
No
GUDID
Yes

Registry differences

EUDAMED and FDA GUDID describe the same product (same UDI-DI) and state different values:

  • Sterilise before use UDI-DI 07290108240566: EUDAMED states No, FDA GUDID states Yes.

Device class is stated on each registry's own scale: Class I in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Vial/bottle adaptor, non-hermetic

Cleared under the same submission (K001293)

and 8 more cleared under K001293

Similar devices in this category

Other devices filed under SYSTEMS FOR RECONSTITUTION AND ADMINISTRATION OF PHARMACEUTICALS.

Other devices from West Pharma. Services IL, Ltd.

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

Properties

  • Supplied sterile
  • Sterilise before use NoEUDAMEDYesGUDID
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (17, all answered No)