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AirLife™

FDA UDI

Class II (US FDA UDI)

by Airlife, Inc.

Identity

Trade Name
AirLife™ FDA UDI
Generic Name
Nasal oxygen cannula, basic FDA UDI
Device Name
AirLife™ Nasal ETCO2 Cannula, Adult with 14' O2 tube and 14' CO2 tube with male luer connector and 22 mm (I.D.) x 6 mm (O.D.) adaptor FDA UDI
Model / Reference
2812M14-25 FDA UDI
Description
AirLife™ Nasal ETCO2 Cannula, Adult with 14' O2 tube and 14' CO2 tube with male luer connector and 22 mm (I.D.) x 6 mm (O.D.) adaptor FDA UDI

Identifiers

Catalog Number
2812M14-25 FDA UDI
Primary DI / UDI-DI
10190752157286 FDA UDI
FDA Product Code
CCK FDA UDI
GMDN Term
Nasal oxygen cannula, basic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1400 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Nasal oxygen cannula, basic

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

Similar devices

Also classified as Nasal oxygen cannula, basic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Airlife, Inc.

Sources (1)

  • FDA UDI 18571711-c6b9-4576-a0a9-9c3f386f4ba6 35 fields · synced May 30, 2026