Puritan Bennett 980NEOFLT
by Covidien LP
Puritan Bennett 980NEOFLT is a Class II device made by Covidien LP, listed in FDA GUDID since 30 Sep 2022 (UDI-DI 10884521803305), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10884521803305 | Date30 Sep 2022 | StatusListed |
Official records
- AccessGUDID record 10884521803305
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Puritan Bennett
- Generic name
- Ventilator application software
- Model / reference
- 980NEOFLT
- Primary DI / UDI-DI
- 10884521803305
- FDA product code
- CBK
- GMDN term
- Ventilator application software
- Device class
- Class II
- Regulation number
- 868.5895
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code CBK (Ventilator, continuous, facility use).
- BIRD AVEA VENTILATOR by Bird Products Corp.
- BREATHE TECHNOLOGIES LIFE2000 VENTILATION SYSTEM by Breathe Technologies, Inc.
- MODIFICATION TO INSPIRATION VENTILATOR SYSTEM by eVent Medical, Ltd.
- Patient Circuit V64-0048 by FLIGHT MEDICAL INNOVATIONS LTD
- VENTILATOR WITH RESPIRATORY MECHANICS, MODEL 840 by Puritan Bennett Corp.
- VENTIMETER VENTILATOR by Narco Air-Shields
- ATLANTIS HYPERBARIC CHAMBER VENTILATOR by Providence Global Medical, Inc.
- NELLCOR PURITAN BENNETT ACHIEVA VENTILATOR AND REPORT GENERATOR by Nellcor Puritan Bennett, Inc.
- TRILOGY SERIES VENTILATOR WITH OXIMETRY by Respironics, Inc.
- GE DATEX-OHMEDA ENGSTROM CARESTATION by Datex-Ohmeda Inc.