Skip to content

Arthrex® AR-7010

by Arthrex, Inc.

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

Ref AR-7010

Arthrex AR-7010 is a tendon/ligament graft preparation station (EU MDR Class I; FDA Class I; FDA product code MDM, Instrument, Manual, Surgical, General Use) made by Arthrex, Inc., registered in EUDAMED on 27 Oct 2026 (Basic UDI-DI 0888867MeasGuideInstNS0KH) and listed in FDA GUDID since 2 Jun 2018 (UDI-DI 00888867207202), 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 Number0888867MeasGuideInstNS0KH Basic UDI-DI 00888867207202UDI-DIDate27 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00888867207202 UDI-DI Date2 Jun 2018ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0888867MeasGuideInstNS0KH registered 27 Oct 2026 Active
  • FDA GUDID UDI-DI 00888867207202 listed 2 Jun 2018 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00888867207202
  2. Registered EUDAMED 0888867MeasGuideInstNS0KH

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  • Withdrawn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®
Generic name
Tendon/ligament graft preparation station
Device name
Measure-Guide NS Insts
Model / Ref / Catalog
AR-7010
Primary DI / UDI-DI
00888867207202
Basic UDI-DI
0888867MeasGuideInstNS0KH
FDA product code
MDM
EMDN code
L0922 Orthopaedic surgery guides, reusable
GMDN term
Tendon/ligament graft preparation station
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: Tendon/ligament graft preparation station

Similar devices in this category

Other devices filed under ORTHOPAEDIC SURGERY GUIDES, REUSABLE.

Other devices from Arthrex, Inc.

See all devices from Arthrex, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (20, all answered No)