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Hex Driver 907775

by Biomet Orthopedics, Inc.

Ref 907775

Hex Driver 907775 is a Class I device made by Biomet Orthopedics, Inc., registered in EUDAMED on 20 Oct 2026 (Basic UDI-DI B-00887868511295) and listed in FDA GUDID since 23 Jul 2021 (UDI-DI 00887868511295), 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-00887868511295 Basic UDI-DI 00887868511295UDI-DIDate20 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00887868511295 UDI-DI Date23 Jul 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00887868511295 registered 20 Oct 2026 Active
  • FDA GUDID UDI-DI 00887868511295 listed 23 Jul 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00887868511295
  2. Registered EUDAMED B-00887868511295

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  • Withdrawn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
Hex Driver
Generic name
Orthopaedic implant driver
Device name
SM Cannulated Hex Dilator
Model / Ref / Catalog
907775
Primary DI / UDI-DI
00887868511295
Basic UDI-DI
B-00887868511295
FDA product code
HWR
EMDN code
L0915 Spreaders and retractors for orthopaedic surgery, reusable
GMDN term
Orthopaedic implant driver
Device class
Class I
Regulation number
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: Orthopaedic implant driver

Similar devices in this category

Other devices filed under SPREADERS AND RETRACTORS FOR ORTHOPAEDIC SURGERY, REUSABLE.

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)