Identity
- Trade Name
- AirLife™ FDA UDI
- Generic Name
- Venturi oxygen face mask FDA UDI
- Device Name
- AirLife™ Adult Dual Dial Venturi Style Mask With 6 inch (15 cm) Flextube, Color Coded Low and Medium Concentration Dials, High Humidity Adapter/Humidification Hood, 7 feet (2.1 m) Crush Resistant Oxygen Tubing and U/Connect-It Adapter FDA UDI
- Model / Reference
- 001255U FDA UDI
- Description
- AirLife™ Adult Dual Dial Venturi Style Mask With 6 inch (15 cm) Flextube, Color Coded Low and Medium Concentration Dials, High Humidity Adapter/Humidification Hood, 7 feet (2.1 m) Crush Resistant Oxygen Tubing and U/Connect-It Adapter FDA UDI
Identifiers
- Catalog Number
- 001255U FDA UDI
- Primary DI / UDI-DI
- 10889483569566 FDA UDI
- FDA Product Code
- BYG FDA UDI
- GMDN Term
- Venturi oxygen face mask 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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Venturi oxygen face mask
AirLife™ by Airlife, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Airlife, Inc.
Sources (1)
- FDA UDI e4ca752a-de91-45ed-8a4d-4c6f9815fadc 36 fields · synced May 31, 2026