Disposable Anesthesia Circuit 9372
Disposable Anesthesia Circuit 9372 is a Class I device made by Westmed, Inc., listed in FDA GUDID since 30 Jun 2019 (UDI-DI 00709078007064), registry data as of 22 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 | Number00709078007064 | Date30 Jun 2019 | StatusListed |
Official records
- AccessGUDID record 00709078007064
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Disposable Anesthesia Circuit
- Generic name
- Anaesthesia breathing circuit, single-use
- Model / reference
- 9372
- Primary DI / UDI-DI
- 00709078007064
- FDA product code
- OFP, CAH
- GMDN term
- Anaesthesia breathing circuit, single-use
- Device class
- Class I
- Regulation number
- 868.5240, 868.5260
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Heat/moisture exchanger/microbial medical gas filter.
- LuerSafe Adult Angled ThermoShield Bacterial Viral HMEF 038-41-335LSU by FLEXICARE MEDICAL LIMITED
- GIBECK IPN043782 19502 by TELEFLEX INCORPORATED
- DAR 352U5996 by Covidien LP
- ThermoShield HMEF Luer Port Flexi Cath Mount D/Swivel Elbow 038-41-355/315U by FLEXICARE MEDICAL LIMITED
- GIBECK IPN043834 19932 by TELEFLEX INCORPORATED
- DAR 352U5877 by Covidien LP
- Filter/HME TwinStar 9 Plus MP05820 by Drägerwerk AG & Co. KGaA
- Filter/HME TwinStar 90 Plus MP05800 by Drägerwerk AG & Co. KGaA