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1884070RTC

by Medtronic Xomed Inc

1884070RTC is a Class I device made by Medtronic Xomed Inc, listed in FDA GUDID since 13 Oct 2017 (UDI-DI 00643169434585), registry data as of 8 Nov 2026.

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

Source GUDID, synced 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00643169434585 UDI-DI Date13 Oct 2017ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Generic name
Metal/carbide ENT bur, single-use
Model / reference
1884070RTC
Primary DI / UDI-DI
00643169434585
FDA product code
EQJ
GMDN term
Metal/carbide ENT bur, single-use
Device class
Class I
Regulation number
874.4140
GUDID distribution status
In Commercial Distribution
Size
Angle — 70.0 degree
Outer Diameter — 4.0 Millimeter
Length — 13.0 Centimeter

Related devices

Category: Metal/carbide ENT bur, single-use

Other devices from Medtronic Xomed Inc

See all devices from Medtronic Xomed Inc →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (10, all answered No)