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40250228

by Wright Medical Technology, Inc.

Ref 40250228Model 08858251028081UC

40250228 is a Class I device made by Wright Medical Technology, Inc., registered in EUDAMED on 28 Oct 2026 (Basic UDI-DI 08858251028081UC) and listed in FDA GUDID since 17 Sep 2016 (UDI-DI 00889797010733), active as of 7 Nov 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 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08858251028081UC Basic UDI-DI 00889797010733UDI-DIDate28 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00889797010733 UDI-DI Date17 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08858251028081UC registered 28 Oct 2026 Active
  • FDA GUDID UDI-DI 00889797010733 listed 17 Sep 2016 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00889797010733
  2. Registered EUDAMED 08858251028081UC

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  • Withdrawn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
Claw® II
Generic name
Surgical instrument guard, reusable
Device name
CLAW II Instrumentation - Instrumentation Sleeves - Class Ir - Reusable - Nonsterile
Model / Ref / Catalog
40250228, 08858251028081UC
Primary DI / UDI-DI
00889797010733
Basic UDI-DI
08858251028081UC
Direct marketing DI
00889797010733
FDA product code
MDM
EMDN code
L091199 Orthopaedic prosthetics instruments, reusable - other
GMDN term
Surgical instrument guard, 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

Similar devices in this category

Other devices filed under ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER.

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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)