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AirLife™

FDA UDI

Class I (US FDA UDI)

by Airlife, Inc.

Identity

Trade Name
AirLife™ FDA UDI
Generic Name
Respiratory gas thermometer FDA UDI
Device Name
AirLife™ Tempo2-I™ Thermometer with U/Adapt-It™ Straight Connector 004086 (Both Arms 22 mm OD) FDA UDI
Model / Reference
001951 FDA UDI
Description
AirLife™ Tempo2-I™ Thermometer with U/Adapt-It™ Straight Connector 004086 (Both Arms 22 mm OD) FDA UDI

Identifiers

Catalog Number
001951 FDA UDI
Primary DI / UDI-DI
10889483570869 FDA UDI
FDA Product Code
FQZ FDA UDI
GMDN Term
Respiratory gas thermometer FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.2900 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Respiratory gas thermometer

AirLife™ by Airlife, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Respiratory gas thermometer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Airlife, Inc.

Sources (1)

  • FDA UDI f8d52cc4-4e70-437d-8501-6c50908d0d3f 35 fields · synced May 30, 2026