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Alloclassic® Zweymüller® 01.00121.060

by Zimmer, Inc. 2 variants

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00889024590410 UDI-DI Date28 Jan 2022ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Alloclassic® Zweymüller®
Generic Name
Press-fit hip femur prosthesis, modular
Model / Ref / Catalog
01.00121.060
Primary DI / UDI-DI
00889024590410
FDA Product Code
JDI, KWL, LZO, KWY
GMDN Term
Press-fit hip femur prosthesis, modular
Device Class
Class II
Regulation Number
888.3350, 888.3360, 888.3353, 888.3390
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional

Related devices

Category: Press-fit hip femur prosthesis, modular

Other devices from Zimmer, Inc.

See all devices from Zimmer, Inc. →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No