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MultiPolar® 5003-40-22

by Zimmer, Inc.

MultiPolar® 5003-40-22 (00-5003-040-22) is a Class I device made by Zimmer, Inc., listed in FDA GUDID since 9 Aug 2016 (UDI-DI 00889024115880), 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 Number00889024115880 UDI-DI Date9 Aug 2016ListedStatusListed 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  • Withdrawn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
MultiPolar®
Generic name
Acetabulum prosthesis trial, prefabricated, reusable
Model / Ref / Catalog
5003-40-22, 00-5003-040-22
Primary DI / UDI-DI
00889024115880
FDA product code
HWT
GMDN term
Acetabulum prosthesis trial, prefabricated, reusable
Device class
Class I
Regulation number
888.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Lumen/Inner Diameter — 22 Millimeter

Related devices

Category: Acetabulum prosthesis trial, prefabricated, reusable

Other devices from Zimmer, Inc.

See all devices from Zimmer, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)