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AirLife™

FDA UDI

Class I (US FDA UDI)

by Airlife, Inc.

Identity

Trade Name
AirLife™ FDA UDI
Generic Name
Tracheobronchial suction/insufflation catheter, single-lumen FDA UDI
Device Name
AirLife Closed Suction Catheter–Tracheostomy Length 14 Fr FDA UDI
Model / Reference
CSC114T FDA UDI
Description
AirLife Closed Suction Catheter–Tracheostomy Length 14 Fr FDA UDI

Identifiers

Catalog Number
CSC114T FDA UDI
Primary DI / UDI-DI
10190752140639 FDA UDI
FDA Product Code
BSY FDA UDI
GMDN Term
Tracheobronchial suction/insufflation catheter, single-lumen FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6810 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

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
Sterilization Method
Ethylene Oxide FDA UDI

Category: Tracheobronchial suction/insufflation catheter, single-lumen

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

Similar devices

Also classified as Tracheobronchial suction/insufflation catheter, single-lumen.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Airlife, Inc.

Sources (1)

  • FDA UDI 397f6db5-76d7-4dd6-86fd-3338912653d7 35 fields · synced May 30, 2026