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Arthrex® AR-623-42

by Arthrex, Inc.

Part of a family of 38 devices: see the family page

Ref AR-623-42

Arthrex® AR-623-42 is a Class I device made by Arthrex, Inc., registered in EUDAMED on 28 Oct 2026 (Basic UDI-DI 0888867ProtectNS0000000KB) and listed in FDA GUDID since 10 May 2018 (UDI-DI 00888867235762), 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 Number0888867ProtectNS0000000KB Basic UDI-DI 00888867235762UDI-DIDate28 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00888867235762 UDI-DI Date10 May 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0888867ProtectNS0000000KB registered 28 Oct 2026 Active
  • FDA GUDID UDI-DI 00888867235762 listed 10 May 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00888867235762
  2. Registered EUDAMED 0888867ProtectNS0000000KB

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  • Withdrawn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
Arthrex EUDAMED
Arthrex® GUDID
Generic name
Surgical implant/trial-implant/sizer holder, reusable
Device name
Protective - Non-sterile
Model / Ref / Catalog
AR-623-42
Primary DI / UDI-DI
00888867235762
Basic UDI-DI
0888867ProtectNS0000000KB
FDA product code
MDM
EMDN code
Z12019099 Various instruments for general and multidisciplinary surgery - other
GMDN term
Surgical implant/trial-implant/sizer holder, 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: Surgical implant/trial-implant/sizer holder, reusable

Similar devices in this category

Other devices filed under VARIOUS INSTRUMENTS FOR GENERAL AND MULTIDISCIPLINARY SURGERY - OTHER.

Other devices from Arthrex, Inc.

See all devices from Arthrex, Inc. →

Properties

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