AirLife 2K8001
by Carefusion GUDID
Withdrawn
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10885403170287 | Date24 Oct 2015 | StatusWithdrawn |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — GUDID listing Listed
Recalls
No FDA recalls on record, checked 23 Oct 2026.
Specification
- Trade Name
- AirLife
- Generic Name
- Pulmonary resuscitator, manual, single-use
- Model / Ref / Catalog
- 2K8001
- Primary DI / UDI-DI
- 10885403170287
- FDA Product Code
- OEV
- GMDN Term
- Pulmonary resuscitator, manual, single-use
- Device Class
- Class II
- Regulation Number
- 868.5915
- Commercial Distribution
- Not in Commercial Distribution
- Size
- Weight — .50 KilogramTotal Volume — 2100.00 Milliliter
Other devices from Carefusion
Properties
Other properties (9)
- Sterile: No
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Manufacturing Date: No