Expiratory valve set 160176
Ref 160176
Expiratory valve set 160176 is a Class I device made by Hamilton Medical AG, registered in EUDAMED on 2 Sep 2026 (Basic UDI-DI 76300028PN1601762X) and listed in FDA GUDID since 8 Dec 2022 (UDI-DI 07630002810432), active as of 9 Nov 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None, self-declared
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number76300028PN1601762X 07630002810432 | Date2 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number07630002810432 | Date8 Dec 2022 | StatusListed |
Official records
- EUDAMED public site 76300028PN1601762X
- AccessGUDID record 07630002810432
Across registries
- EUDAMED Basic UDI-DI 76300028PN1601762X registered 2 Sep 2026 Active
- FDA GUDID UDI-DI 07630002810432 listed 8 Dec 2022 Listed
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Timeline
- Listed FDA GUDID 07630002810432
- Registered EUDAMED 76300028PN1601762X
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Expiratory valve set for HAMILTON-C2/C3/C6, single use EUDAMEDExpiratory valve set GUDID
- Generic name
- Mechanical expiratory valve, single-use
- Model / reference
- 160176
- Primary DI / UDI-DI
- 07630002810432
- Basic UDI-DI
- 76300028PN1601762X
- FDA product code
- BYX
- EMDN code
- R9080 Respiratory and anesthesia devices - accessories not included in other classes
- GMDN term
- Mechanical expiratory valve, single-use
- Device class
- Class I
- Regulation number
- 868.5860
- EU registration type
- Standard device
- EU market of registration
- Austria
- GUDID distribution status
- In Commercial Distribution