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AirLife™

FDA UDI

Class I (US FDA UDI)

by Airlife, Inc.

Identity

Trade Name
AirLife™ FDA UDI
Generic Name
Inspiratory line humidification chamber, single-use FDA UDI
Device Name
AirLife™ Infant Single Limb Heated Wire Circuit Kit Single-limb, Single-heated, continuous-flow circuit (>4 L/min) Contains AH032 Circuit, AH290 Chamber FDA UDI
Model / Reference
AH132 FDA UDI
Description
AirLife™ Infant Single Limb Heated Wire Circuit Kit Single-limb, Single-heated, continuous-flow circuit (>4 L/min) Contains AH032 Circuit, AH290 Chamber FDA UDI

Identifiers

Catalog Number
AH132 FDA UDI
Primary DI / UDI-DI
10889483595855 FDA UDI
FDA Product Code
OFP FDA UDI
GMDN Term
Inspiratory line humidification chamber, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5240 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Inspiratory line humidification chamber, single-use

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

Similar devices

Also classified as Inspiratory line humidification chamber, 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 608ce601-b122-416e-b7ba-a6a6683ac6e1 35 fields · synced Jun 8, 2026