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AirLife™

FDA UDI

Class II (US FDA UDI)

by Airlife, Inc.

Identity

Trade Name
AirLife™ FDA UDI
Generic Name
Microbial medical gas filter, single-use FDA UDI
Device Name
AirLife™ Bacterial/Viral Filter FDA UDI
Model / Reference
303EU FDA UDI
Description
AirLife™ Bacterial/Viral Filter FDA UDI

Identifiers

Catalog Number
303EU FDA UDI
Primary DI / UDI-DI
10190752148789 FDA UDI
FDA Product Code
CAH FDA UDI
GMDN Term
Microbial medical gas filter, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5260 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Microbial medical gas filter, single-use

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

Similar devices

Also classified as Microbial medical gas filter, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Airlife, Inc.

Sources (1)

  • FDA UDI 7559633d-b20f-4b37-8d45-92e73710f7a3 35 fields · synced May 30, 2026