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Retractor 75.22.06

by Zimmer, Inc.

Part of a family of 18 devices: see the family page

Ref 75.22.06

Retractor 75.22.06 is a Class I device made by Zimmer, Inc., registered in EUDAMED on 19 Oct 2026 (Basic UDI-DI 889024AC4Y2) and listed in FDA GUDID since 30 Jun 2020 (UDI-DI 00889024303072), active as of 25 Oct 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number889024AC4Y2 Basic UDI-DI 00889024303072UDI-DIDate19 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00889024303072 UDI-DI Date30 Jun 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 889024AC4Y2 registered 19 Oct 2026 Active
  • FDA GUDID UDI-DI 00889024303072 listed 30 Jun 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00889024303072
  2. Registered EUDAMED 889024AC4Y2

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  • Withdrawn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
Retractor
Generic name
Joint prosthesis implantation kit, reusable
Model / Ref / Catalog
75.22.06
Primary DI / UDI-DI
00889024303072
Basic UDI-DI
889024AC4Y2
Direct marketing DI
00889024303072
FDA product code
GAD
EMDN code
L091103 Orthopaedic prostheses forceps, reusable
GMDN term
Joint prosthesis implantation kit, reusable
Device class
Class I
Regulation number
878.4800
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: Joint prosthesis implantation kit, reusable

Similar devices in this category

Other devices filed under ORTHOPAEDIC PROSTHESES FORCEPS, REUSABLE.

Other devices from Zimmer, Inc.

See all devices from Zimmer, Inc. →

Properties

  • Sterilise before use
  • Reusable
  • Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction)
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (18, all answered No)