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Tendon Stripper 909990

by Biomet Orthopedics, Inc.

Ref 909990

Tendon Stripper 909990 is a tendon stripper (EU MDD Class I; FDA Class I; FDA product code HRT, Stripper, Surgical) made by Biomet Orthopedics, Inc., registered in EUDAMED on 20 Oct 2026 (Basic UDI-DI B-00887868511738) and listed in FDA GUDID since 23 Jul 2021 (UDI-DI 00887868511738), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-00887868511738 Basic UDI-DI 00887868511738UDI-DIDate20 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00887868511738 UDI-DI Date23 Jul 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-00887868511738 registered 20 Oct 2026 Active
  • FDA GUDID UDI-DI 00887868511738 listed 23 Jul 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00887868511738
  2. Registered EUDAMED B-00887868511738

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  • Withdrawn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
Tendon Stripper
Generic name
Tendon stripper
Device name
SM Closed Tendon Stripper
Model / Ref / Catalog
909990
Primary DI / UDI-DI
00887868511738
Basic UDI-DI
B-00887868511738
FDA product code
HRT
EMDN code
L091199 Orthopaedic prosthetics instruments, reusable - other
GMDN term
Tendon stripper
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: Tendon stripper

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)