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Drivemedical

FDA UDI

Class II (US FDA UDI)

by Drive Devilbiss Healthcare

Identity

Trade Name
DRIVEMEDICAL FDA UDI
Generic Name
Pulse Co-oximeter FDA UDI
Device Name
RespiratoryPulse Oximeters Product Description: Pediatric Pulse Oximeter, 1/ea FDA UDI
Model / Reference
18707 FDA UDI
Description
RespiratoryPulse Oximeters Product Description: Pediatric Pulse Oximeter, 1/ea FDA UDI

Identifiers

Primary DI / UDI-DI
00822383529554 FDA UDI
FDA Product Code
DQA 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

No

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

Drivemedical 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 a724033b-16e8-41e4-809c-73718b63ee60 33 fields · synced Jun 8, 2026