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Thin Latarjet Retractor

by Innomed, Inc.

Ref 5256-01

Thin Latarjet Retractor (5256-01) is a Class I device made by Innomed, Inc., registered in EUDAMED on 18 Mar 2022 (Basic UDI-DI 8402771INNORETRACT016A) and listed in FDA GUDID since 29 May 2026 (UDI-DI 00840277133663), 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
United StatesGUDID listing GUDID Number00840277133663 UDI-DI Date29 May 2026ListedStatusListed GUDID: in commercial distribution
European UnionCE/MDR EUDAMED Number8402771INNORETRACT016A Basic UDI-DI 00840277133663UDI-DIDate18 Mar 2022RegisteredStatusActive

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 8402771INNORETRACT016A registered 18 Mar 2022 Active
  • FDA GUDID UDI-DI 00840277133663 listed 29 May 2026 Listed

Timeline

2 dated events

  1. Registered EUDAMED 8402771INNORETRACT016A
  2. Listed FDA GUDID 00840277133663

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  • Withdrawn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
Thin Latarjet Retractor EUDAMED
Innomed, Inc. GUDID
Generic name
Hand-held surgical retractor, reusable
Device name
Retractor
Model / Ref / Catalog
5256-01
Primary DI / UDI-DI
00840277133663
Basic UDI-DI
8402771INNORETRACT016A
Direct marketing DI
00840277133663
FDA product code
GAD
EMDN code
L0915 Spreaders and retractors for orthopaedic surgery, reusable
GMDN term
Hand-held surgical retractor, reusable
Device class
Class I
Regulation number
878.4800
System or procedure pack
System which is a device in itself
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Manufacturer details

EUDAMED SRN
US-MF-000014761
Authorised representative
MediMark Europe Sarl. FR-AR-000000182

Similar devices in this category

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

Other devices from Innomed, Inc.

See all devices from Innomed, Inc. →

Properties

  • Sterilise before use
  • Reusable
  • Premarket exempt
Other properties (22, all answered No)