RespiraSense
Ref RSV4
Active
CE MDR 510(k)
Valid until
Not listed
FDA recalls
None foundTrust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number53915332900RespirasenseDK | Date13 Jun 2024 | StatusActive |
| United States | FDA 510(k) 510(k) | NumberK220111 | Date7 Oct 2022 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Recalls
No FDA recalls found in the data synced 24 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- United States
- European Union
Specification
- Device Name
- RespiraSense patient respiratory monitor system.
- Model / Reference
- RSV4
- Primary DI / UDI-DI
- 05391533290002, 05391533290057, 05391533290019
- Basic UDI-DI
- 53915332900RespirasenseDK
- Direct Marketing DI
- 053915332900020539153329005705391533290019
- EMDN Code
- V0380 Devices with measuring functions - accessories
- Device Class
- Class IIa
- EU market of registration
- Ireland
Manufacturer details
- EUDAMED SRN
- IE-MF-000016708
Other devices from PMD Device Solutions Ltd
Properties
Other properties (12)
- Sterile: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Incorporates Medicinal Product: No