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ACS® UNI LD femoral component cemented 42062104

by implantcast GmbH

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 Number04048844128609 UDI-DI Date12 Jan 2021ListedStatusListed 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  • Withdrawn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
ACS® UNI LD femoral component cemented
Generic Name
Uncoated unicondylar knee femur prosthesis
Model / Reference
42062104
Primary DI / UDI-DI
04048844128609
FDA Product Code
HSX
GMDN Term
Uncoated unicondylar knee femur prosthesis
Device Class
Class II
Regulation Number
888.3520
GUDID distribution status
In Commercial Distribution

Related devices

Category: Uncoated unicondylar knee femur prosthesis

Other devices from implantcast GmbH

See all devices from implantcast GmbH →

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