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Na 1133372

by Medtronic Xomed, Inc. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00681490034708 UDI-DIDate22 Jun 2015ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Generic Name
Ossicular prosthesis, partial
Model / Reference
1133372
Primary DI / UDI-DI
00681490034708
FDA Product Code
ETA
GMDN Term
Ossicular prosthesis, partial
Device Class
Class II
Regulation Number
874.3495
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional
Size
Length — 4.25 Millimeter

Related devices

Category: Ossicular prosthesis, partial

Other devices from Medtronic Xomed, Inc.

See all devices from Medtronic Xomed, Inc. →

Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number

Other properties (8)

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