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G7® 110017262

by Biomet Orthopedics, Inc.

Ref 110017262

G7® 110017262 is a device classified as Class IIa in the EU and Class II in the US made by Biomet Orthopedics, Inc., registered in EUDAMED on 1 Nov 2026 (Basic UDI-DI B-00887868466489) and listed in FDA GUDID since 22 Jun 2022 (UDI-DI 00887868466489), active as of 7 Nov 2026.

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

CE MDD

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/MDD EUDAMED NumberB-00887868466489 Basic UDI-DI 00887868466489UDI-DIDate1 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00887868466489 UDI-DI Date22 Jun 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00887868466489 registered 1 Nov 2026 Active
  • FDA GUDID UDI-DI 00887868466489 listed 22 Jun 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00887868466489
  2. Registered EUDAMED B-00887868466489

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
G7®
Generic name
Acetabulum prosthesis trial, prefabricated, reusable
Device name
G7 Provisional Standard +5MM Liner
Model / Ref / Catalog
110017262
Primary DI / UDI-DI
00887868466489
Basic UDI-DI
B-00887868466489
FDA product code
OQI, PBI, KWZ, LPH, JDI, OQG, LZO, OQH
EMDN code
L091104 Orthopaedic prostheses positioners, reusable
GMDN term
Acetabulum prosthesis trial, prefabricated, reusable
Device class
Class IIa EUDAMED
Class II GUDID
Regulation number
888.3353, 888.3310, 888.3358, 888.3350
EU registration type
Legacy device (under a directive)
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class II

Device class is stated on each registry's own scale: Class IIa 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: Acetabulum prosthesis trial, prefabricated, 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
  • Prescription use
  • Lot / batch number
Other properties (22, all answered No)