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Vital Signs™

FDA UDI

Class I (US FDA UDI)

by Airlife, Inc.

Identity

Trade Name
Vital Signs™ FDA UDI
Generic Name
Tracheostomy mask, aerosol FDA UDI
Device Name
Adult Tracheostomy Mask FDA UDI
Model / Reference
001225 FDA UDI
Description
Adult Tracheostomy Mask FDA UDI

Identifiers

Catalog Number
001225 FDA UDI
Primary DI / UDI-DI
10889483569412 FDA UDI
FDA Product Code
BYG FDA UDI
GMDN Term
Tracheostomy mask, aerosol FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5580 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Tracheostomy mask, aerosol

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

Similar devices

Also classified as Tracheostomy mask, aerosol.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Airlife, Inc.

Sources (1)

  • FDA UDI e335c8ea-7c67-490d-b52a-7b9c9afdc1ec 35 fields · synced May 31, 2026