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Arthrex® AR-1981-08H

by Arthrex, Inc.

Arthrex® AR-1981-08H is a Class I device made by Arthrex, Inc., listed in FDA GUDID since 30 May 2018 (UDI-DI 00888867025325), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00888867025325 UDI-DI Date30 May 2018ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Arthrex®
Generic name
Bone graft delivery kit
Model / Ref / Catalog
AR-1981-08H
Primary DI / UDI-DI
00888867025325
FDA product code
LXH
GMDN term
Bone graft delivery kit
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution

Related devices

Category: Bone graft delivery kit

Similar devices

Other devices filed under FDA product code LXH (ORTHOPEDIC MANUAL SURGICAL INSTRUMENT).

Other devices from Arthrex, Inc.

See all devices from Arthrex, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)