Skip to content

Vanguard® Knee System

by Biomet UK Ltd 2 variants

Ref 32-422995

Vanguard® Knee System (32-422995) is a Class I device made by Biomet UK Ltd., registered in EUDAMED on 3 Sep 2026 (Basic UDI-DI 889024E0GZ), active as of 22 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number889024E0GZ Basic UDI-DI 05019279442317UDI-DIDate3 Sep 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Knee Instrument Cases
Model / reference
32-422995
Primary DI / UDI-DI
05019279442317
Basic UDI-DI
889024E0GZ
EMDN code
L091104 Orthopaedic prostheses positioners, reusable
Device class
Class I
EU registration type
Standard device
EU market of registration
Netherlands

Manufacturer details

EUDAMED SRN
GB-MF-000001894
Authorised representative
Biomet Global Supply Chain Center B.V. NL-AR-000000422

Similar devices in this category

Other devices filed under ORTHOPAEDIC PROSTHESES POSITIONERS, REUSABLE.

Other devices from Biomet UK Ltd.

See all devices from Biomet UK Ltd. →

Properties

  • Reusable
Other properties (13, all answered No)