← Back to catalogue

AirLife™ Adult Oxygen Mask Vinyl, Under the Chin Style

FDA UDI

Class I (US FDA UDI)

by Vyaire Medical, Inc.

Identity

Trade Name
AirLife™ Adult Oxygen Mask Vinyl, Under the Chin Style FDA UDI
Generic Name
Rebreathing oxygen face mask FDA UDI
Device Name
AirLife™ Adult Oxygen Mask Vinyl, Under the Chin Style, High Concentration Rebreather Mask (No Valves) with 7 feet (2.1 m) Crush Resistant Oxygen Tubing FDA UDI
Model / Reference
001205 FDA UDI
Description
AirLife™ Adult Oxygen Mask Vinyl, Under the Chin Style, High Concentration Rebreather Mask (No Valves) with 7 feet (2.1 m) Crush Resistant Oxygen Tubing FDA UDI

Identifiers

Catalog Number
001205 FDA UDI
Primary DI / UDI-DI
10190752116344 FDA UDI
FDA Product Code
CAT FDA UDI
GMDN Term
Rebreathing oxygen face mask FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5340 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

No

FDA UDI

Category: Rebreathing oxygen face mask

AirLife™ Adult Oxygen Mask Vinyl, Under the Chin Style by Vyaire Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rebreathing oxygen face mask.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 484d1035-4e13-42b4-a0e2-cf8f0c94437e 35 fields · synced Jun 1, 2026