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Arthrex® ABS-10024

by Arthrex, Inc.

Arthrex® ABS-10024 is a Class I device made by Arthrex, Inc., listed in FDA GUDID since 26 Jul 2018 (UDI-DI 10888867001906), 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 Number10888867001906 UDI-DI Date26 Jul 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  • Withdrawn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
Centrifuge bucket/tube holder
Model / Ref / Catalog
ABS-10024
Primary DI / UDI-DI
10888867001906
FDA product code
JQC
GMDN term
Centrifuge bucket/tube holder
Device class
Class I
Regulation number
862.2050
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Centrifuge bucket/tube holder

Similar devices

Other devices filed under FDA product code JQC (CENTRIFUGES (MICRO, ULTRA, REFRIGERATED) FOR CLINICAL USE).

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 (10, all answered No)