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Anatomical Shoulder™ 01.04215.183

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 Number00889024484849 UDI-DI Date28 Jul 2017ListedStatusListed 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  • Withdrawn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
Anatomical Shoulder™
Generic Name
Total shoulder prosthesis
Model / Ref / Catalog
01.04215.183
Primary DI / UDI-DI
00889024484849
FDA Product Code
PHX, KWT, KWS, HSD
GMDN Term
Total shoulder prosthesis
Device Class
Class II
Regulation Number
888.3660, 888.3650, 888.3690
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional
Size
Length — 200 Millimeter
Outer Diameter — 18 Millimeter

Other devices from Zimmer, Inc.

See all devices from Zimmer, Inc. →

Properties

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

Other properties (8)

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