Identity
- Trade Name
- AirLife™ FDA UDI
- Generic Name
- Rebreathing oxygen face mask FDA UDI
- Device Name
- AirLife™ Pediatric Oxygen Mask Vinyl, Short Style, High Concentration, Rebreather Mask (No Valves) with 7 feet (2.1 m) Crush Resistant Oxygen Tubing FDA UDI
- Model / Reference
- 001265 FDA UDI
- Description
- AirLife™ Pediatric Oxygen Mask Vinyl, Short Style, High Concentration, Rebreather Mask (No Valves) with 7 feet (2.1 m) Crush Resistant Oxygen Tubing FDA UDI
Identifiers
- Catalog Number
- 001265 FDA UDI
- Primary DI / UDI-DI
- 10889483569672 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™ by Airlife, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- ClasStar, GanzGesMask, NIV, AAV, L — Drägerwerk AG & Co. KGaA · Class IIa
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- Oro-Nasal Mask — HANS RUDOLPH, INC. · Class IIa
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 4c427d44-33d4-46d0-97a0-7321db5e3795 35 fields · synced Jun 1, 2026