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Vanguard® 32-486822

by Biomet Orthopedics, Inc.

Ref 32-486822

Vanguard® 32-486822 is a Class I device made by Biomet Orthopedics, Inc., registered in EUDAMED on 31 Oct 2026 (Basic UDI-DI 889024BHFZQ) and listed in FDA GUDID since 19 Mar 2022 (UDI-DI 00887868495168), active as of 7 Nov 2026.

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

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number889024BHFZQ Basic UDI-DI 00887868495168UDI-DIDate31 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00887868495168 UDI-DI Date19 Mar 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 889024BHFZQ registered 31 Oct 2026 Active
  • FDA GUDID UDI-DI 00887868495168 listed 19 Mar 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00887868495168
  2. Registered EUDAMED 889024BHFZQ

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
Vanguard®
Generic name
Bone-resection orthopaedic reamer, reusable
Device name
Vanguard Three Peg 25_31 Patellar Drill Guide
Model / Ref / Catalog
32-486822
Primary DI / UDI-DI
00887868495168
Basic UDI-DI
889024BHFZQ
Direct marketing DI
00887868495168
FDA product code
LXH
EMDN code
L091104 Orthopaedic prostheses positioners, reusable
GMDN term
Bone-resection orthopaedic reamer, reusable
Device class
Class I
Regulation number
888.4540
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Bone-resection orthopaedic reamer, reusable

Similar devices in this category

Other devices filed under ORTHOPAEDIC PROSTHESES POSITIONERS, REUSABLE.

Other devices from Biomet Orthopedics, Inc.

See all devices from Biomet Orthopedics, Inc. →

Properties

  • Sterilise before use
  • Reusable
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction)
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (19, all answered No)