Identity
- Trade Name
- AirLife™ FDA UDI
- Generic Name
- Straight/elbow breathing circuit connector, single-use FDA UDI
- Device Name
- AirLife™ Ventilator Elbow with Suction Port and Cap 22 mm I.D. x 22 mm O.D. Inlet Arm, 15 mm I.D. Base FDA UDI
- Model / Reference
- 001550 FDA UDI
- Description
- AirLife™ Ventilator Elbow with Suction Port and Cap 22 mm I.D. x 22 mm O.D. Inlet Arm, 15 mm I.D. Base FDA UDI
Identifiers
- Catalog Number
- 001550 FDA UDI
- Primary DI / UDI-DI
- 10889483570425 FDA UDI
- FDA Product Code
- CAT FDA UDI
- GMDN Term
- Straight/elbow breathing circuit connector, single-use 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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Straight/elbow breathing circuit connector, single-use
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 9b96d648-1e7b-4d46-ba3f-6d3116df9e77 35 fields · synced May 30, 2026