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Arthrex® AR-1747-B

by Arthrex, Inc.

Part of a family of 44 devices: see the family page

Ref AR-1747-B

Arthrex® AR-1747-B is a Class I device made by Arthrex, Inc., registered in EUDAMED on 26 Oct 2026 (Basic UDI-DI 0888867PosInstsNS0000003P) and listed in FDA GUDID since 12 Mar 2019 (UDI-DI 00888867290808), 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 Number0888867PosInstsNS0000003P Basic UDI-DI 00888867290808UDI-DIDate26 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00888867290808 UDI-DI Date12 Mar 2019ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0888867PosInstsNS0000003P registered 26 Oct 2026 Active
  • FDA GUDID UDI-DI 00888867290808 listed 12 Mar 2019 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 00888867290808
  2. Registered EUDAMED 0888867PosInstsNS0000003P

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  • Withdrawn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
Leg procedure positioner
Device name
Positioning NS Insts
Model / Ref / Catalog
AR-1747-B
Primary DI / UDI-DI
00888867290808
Basic UDI-DI
0888867PosInstsNS0000003P
FDA product code
BWN
EMDN code
Z12011299 Patient positioning instruments – other
GMDN term
Leg procedure positioner
Device class
Class I
Regulation number
878.4950
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: Leg procedure positioner

Similar devices in this category

Other devices filed under PATIENT POSITIONING INSTRUMENTS – OTHER.

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)