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AirLife™

FDA UDI

Class II (US FDA UDI)

by Airlife, Inc.

Identity

Trade Name
AirLife™ FDA UDI
Generic Name
Straight/elbow breathing circuit connector, single-use FDA UDI
Device Name
AirLife™ Adult "Y" Connector with Elbow Thermometer and Pressure Sensing Ports with Caps FDA UDI
Model / Reference
001831 FDA UDI
Description
AirLife™ Adult "Y" Connector with Elbow Thermometer and Pressure Sensing Ports with Caps FDA UDI

Identifiers

Catalog Number
001831 FDA UDI
Primary DI / UDI-DI
10889483570692 FDA UDI
FDA Product Code
BWF FDA UDI
GMDN Term
Straight/elbow breathing circuit connector, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5690 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Straight/elbow breathing circuit connector, single-use

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

Similar devices

Also classified as Straight/elbow breathing circuit connector, 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 8bf52435-b428-455f-8628-c1f7629b8ad9 35 fields · synced May 31, 2026