Skip to content

N/A 1884032

by Medtronic Xomed, 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 Number00681490615280 UDI-DIDate13 Oct 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  • Withdrawn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

Generic Name
Surgical saw blade, oscillating, single-use
Model / Reference
1884032
Primary DI / UDI-DI
00681490615280
FDA Product Code
EQJ
GMDN Term
Surgical saw blade, oscillating, single-use
Device Class
Class I
Regulation Number
874.4140
GUDID distribution status
In Commercial Distribution
Size
Length — 37.0 Centimeter
Outer Diameter — 4.0 Millimeter

Related devices

Category: Surgical saw blade, oscillating, single-use

Other devices from Medtronic Xomed, Inc.

See all devices from Medtronic Xomed, Inc. →

Properties

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

Other properties (9)

  • 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