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Precision 110004080

by Biomet Orthopedics, Inc.

Ref 110004080

Precision 110004080 is a Class I device made by Biomet Orthopedics, Inc., registered in EUDAMED on 20 Oct 2026 (Basic UDI-DI B-00887868462764) and listed in FDA GUDID since 2 Apr 2021 (UDI-DI 00887868462764), active as of 23 Oct 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00887868462764 Basic UDI-DI 00887868462764UDI-DIDate20 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00887868462764 UDI-DI Date2 Apr 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00887868462764 registered 20 Oct 2026 Active
  • FDA GUDID UDI-DI 00887868462764 listed 2 Apr 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00887868462764
  2. Registered EUDAMED B-00887868462764

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  • Withdrawn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
Precision
Generic name
Surgical drill guide, reusable
Device name
SM Precision MPF Universal Aimer
Model / Ref / Catalog
110004080
Primary DI / UDI-DI
00887868462764
Basic UDI-DI
B-00887868462764
FDA product code
FZX, LXH
EMDN code
L091199 Orthopaedic prosthetics instruments, reusable - other
GMDN term
Surgical drill guide, reusable
Device class
Class I
Regulation number
878.4800, 888.4540
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

Related devices

Category: Surgical drill guide, reusable

Similar devices in this category

Other devices filed under ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER.

Other devices from Biomet Orthopedics, Inc.

See all devices from Biomet Orthopedics, Inc. →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (20, all answered No)