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N/A 3121584

by Medtronic Xomed, Inc. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00681490069625 UDI-DIDate8 Sep 2017ListedStatusListed 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  • Withdrawn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
Orthopaedic bur, reusable
Model / Reference
3121584
Primary DI / UDI-DI
00681490069625
FDA Product Code
EQJ
GMDN Term
Orthopaedic bur, reusable
Device Class
Class I
Regulation Number
874.4140
GUDID distribution status
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization
Size
Length — 75.0 Millimeter
Outer Diameter — 4.0 Millimeter

Related devices

Category: Orthopaedic bur, reusable

Other devices from Medtronic Xomed, Inc.

See all devices from Medtronic Xomed, Inc. →

Properties

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

Other properties (10)

  • Single Use: No
  • Implantable: No
  • 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