Ventrio
by Davol Inc., Subsidiary of C.R. Bard, Inc. 9 variants
Ref 5950070G
Active
CE MDR
Valid until
8 Sep 2031
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | NumberMDR 731915 | Date24 Aug 2026 | StatusActive |
Certificates
- MDR 731915 Active
Technical documentation EU MDR
- Certifier
- BSI Group The Netherlands B.V. 2797
- Issued
- 24 Aug 2026
- Expires
- 8 Sep 2031
- Valid from
- 9 Sep 2026
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Ventrio ST Hernia Patch
- Model / Reference
- 5950070G
- Primary DI / UDI-DI
- 00801741183775
- Basic UDI-DI
- 0801741XEJFJBHPW9
- EMDN Code
- P900204 Surgical meshes, more than one component
- Device Class
- Class III
- EU market of registration
- Belgium
Manufacturer details
- EUDAMED SRN
- US-MF-000017971
- Authorised representative
- Becton Dickinson Ireland Limited IE-AR-000007610
Other devices from Davol Inc., Subsidiary of C.R. Bard, Inc.
See all devices from Davol Inc., Subsidiary of C.R. Bard, Inc. →
Properties
Other properties (11)
- 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
- Measuring Function: No
- Incorporates Medicinal Product: No