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AirLife™

FDA UDI

Class II (US FDA UDI)

by Airlife, Inc.

Identity

Trade Name
AirLife™ FDA UDI
Generic Name
Tracheostomy care kit, single-use FDA UDI
Device Name
Mini Tracheostomy Care Kit FDA UDI
Model / Reference
3T3030A FDA UDI
Description
Mini Tracheostomy Care Kit FDA UDI

Identifiers

Catalog Number
3T3030A FDA UDI
Primary DI / UDI-DI
10190752141940 FDA UDI
FDA Product Code
CAF FDA UDI
GMDN Term
Tracheostomy care kit, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5630 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

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: Tracheostomy care kit, single-use

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

Similar devices

Also classified as Tracheostomy care kit, 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 e583a036-e31c-4f08-9585-008274858a0b 35 fields · synced Jun 8, 2026