VenusP-Valve System
by Venus Medtech (Hangzhou) Inc. MF 10 variants
Ref P28-30Model L28P,L30P,L32P,L34P,L36P
Expiring
CE MDR
Valid until
1 Apr 2027
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number2245375CE01 | Date19 Aug 2026 | StatusExpiring |
Certificates
- 2245375CE01 Expiring
Quality management system EU MDR
- Certifier
- DEKRA Certification B.V. 0344
- Issued
- 19 Aug 2026
- Expires
- 1 Apr 2027
- Reason
- Other
- 2245375TD01 Expiring
Technical documentation EU MDR
- Certifier
- DEKRA Certification B.V. 0344
- Issued
- 6 Nov 2025
- Expires
- 1 Apr 2027
- Reason
- Other
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Expiring
Specification
- Device Name
- VenusP-Valve System, Percutaneous Pulmonary Valve
- Model / Reference
- L28P,L30P,L32P,L34P,L36P, P28-30
- Primary DI / UDI-DI
- 06970872490206
- Basic UDI-DI
- 6970872490001BQ
- EMDN Code
- P070301030103 Stented biological pulmonary valves for percutaneous implant - valve tissue of animal origin
- Device Class
- Class III
- EU market of registration
- Austria
Manufacturer details
- EUDAMED SRN
- CN-MF-000021841
- Authorised representative
- Obelis s.a. BE-AR-000000106
Other devices from Venus Medtech (Hangzhou) Inc. MF
Properties
Other properties (10)
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No