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AS univation® XF NO186Z

by Aesculap, Inc.

Listed FDA GUDID listing, not in commercial distribution

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 Number04046964053634 UDI-DI Date24 Sep 2015ListedStatusListed GUDID: not 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  • Withdrawn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
AS univation® XF
Generic Name
Uncoated unicondylar knee femur prosthesis
Model / Ref / Catalog
NO186Z
Primary DI / UDI-DI
04046964053634
FDA Product Code
HRY
GMDN Term
Uncoated unicondylar knee femur prosthesis
Device Class
Class II
Regulation Number
888.3530
GUDID distribution status
Not in Commercial Distribution

Related devices

Category: Uncoated unicondylar knee femur prosthesis

Other devices from Aesculap, Inc.

See all devices from Aesculap, 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