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6836

by Zimmer, Inc.

Part of a family of 6 devices: see the family page

Ref 6836

6836 is a device classified as Class IIa in the EU and Class I in the US made by Zimmer, Inc., registered in EUDAMED on 30 Jun 2026 (Basic UDI-DI 889024GAJ7) and listed in FDA GUDID since 16 Nov 2018 (UDI-DI 00889024301566), active as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number889024GAJ7 Basic UDI-DI 00889024301566UDI-DIDate30 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00889024301566 UDI-DI Date16 Nov 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 889024GAJ7 registered 30 Jun 2026 Active
  • FDA GUDID UDI-DI 00889024301566 listed 16 Nov 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00889024301566
  2. Registered EUDAMED 889024GAJ7

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  • Withdrawn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
Multi System Instruments - Hips (WIN)
Generic name
Femoral head prosthesis trial
Device name
Trial Heads with O-ring
Model / Ref / Catalog
6836
Primary DI / UDI-DI
00889024301566
Basic UDI-DI
889024GAJ7
FDA product code
LXH
EMDN code
L091104 Orthopaedic prostheses positioners, reusable
GMDN term
Femoral head prosthesis trial
Device class
Class IIa EUDAMED
Class I GUDID
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

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class I

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class I in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Femoral head prosthesis trial

Similar devices in this category

Other devices filed under ORTHOPAEDIC PROSTHESES POSITIONERS, REUSABLE.

Other devices from Zimmer, Inc.

See all devices from Zimmer, Inc. →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (19, all answered No)