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Medquip

FDA UDI

Class II (US FDA UDI)

by Drive Devilbiss Healthcare

Identity

Trade Name
Medquip FDA UDI
Generic Name
Pulse Co-oximeter FDA UDI
Device Name
RespiratoryPulse Oximeters Product Description: Fingertip Pulse Oximeter 1/ea FDA UDI
Model / Reference
MQ3000 FDA UDI
Description
RespiratoryPulse Oximeters Product Description: Fingertip Pulse Oximeter 1/ea FDA UDI

Identifiers

Primary DI / UDI-DI
00718122940547 FDA UDI
FDA Product Code
OCH FDA UDI
GMDN Term
Pulse Co-oximeter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2700 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Pulse Co-oximeter

Medquip by Drive Devilbiss Healthcare — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pulse Co-oximeter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Drive Devilbiss Healthcare

Sources (1)

  • FDA UDI 0d465c83-68b5-47eb-8db7-00ef7147469e 33 fields · synced Jun 8, 2026