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N/A 1882940HRE

by Medtronic Xomed, 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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00885074079820 UDI-DI Date13 Oct 2017ListedStatusListed 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  • Withdrawn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

Generic Name
Surgical saw blade, oscillating, single-use
Model / Reference
1882940HRE
Primary DI / UDI-DI
00885074079820
FDA Product Code
EQJ
GMDN Term
Surgical saw blade, oscillating, single-use
Device Class
Class I
Regulation Number
874.4140
GUDID distribution status
Not in Commercial Distribution
Size
Length — 11.0 Centimeter
Outer Diameter — 2.9 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