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Liverpool™ 408030

by Biomet Orthopedics, Inc.

Ref 408030

Liverpool™ 408030 is a Class I device made by Biomet Orthopedics, Inc., registered in EUDAMED on 31 Oct 2026 (Basic UDI-DI 889024-ZB002030-EK) and listed in FDA GUDID since 23 Apr 2022 (UDI-DI 00887868506123), 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 Number889024-ZB002030-EK Basic UDI-DI 00887868506123UDI-DIDate31 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00887868506123 UDI-DI Date23 Apr 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 889024-ZB002030-EK registered 31 Oct 2026 Active
  • FDA GUDID UDI-DI 00887868506123 listed 23 Apr 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00887868506123
  2. Registered EUDAMED 889024-ZB002030-EK

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  • Withdrawn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
Liverpool™
Generic name
Surgical drill guide, reusable
Device name
Liverpl Rad Hd Cutting Jig
Model / Ref / Catalog
408030
Primary DI / UDI-DI
00887868506123
Basic UDI-DI
889024-ZB002030-EK
Direct marketing DI
00887868506123
FDA product code
LXH
EMDN code
L091002 Instruments for processing materials for osteosynthesis, reusable
GMDN term
Surgical drill guide, 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: Surgical drill guide, reusable

Similar devices in this category

Other devices filed under INSTRUMENTS FOR PROCESSING MATERIALS FOR OSTEOSYNTHESIS, 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)