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Medquip MQ3000

by Drive Devilbiss Healthcare

Medquip MQ3000 is a Class II device made by Drive Devilbiss Healthcare, listed in FDA GUDID since 21 Jun 2019 (UDI-DI 00718122940547), registry data as of 22 Oct 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00718122940547 UDI-DI Date21 Jun 2019ListedStatusListed 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  • Withdrawn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

Trade name
Medquip
Generic name
Pulse Co-oximeter
Model / reference
MQ3000
Primary DI / UDI-DI
00718122940547
FDA product code
OCH
GMDN term
Pulse Co-oximeter
Device class
Class II
Regulation number
870.2700
GUDID distribution status
In Commercial Distribution

Related devices

Category: Pulse Co-oximeter

Similar devices

Also classified as Pulse Co-oximeter.

Other devices from Drive Devilbiss Healthcare

See all devices from Drive Devilbiss Healthcare →

Properties

  • Prescription use
  • Premarket exempt
  • Serial number
Other properties (12, all answered No)