iVascular xperience pro
by Life Vascular Devices Biotech, S.L. 74 variants
Ref BCPR14N150500010Model xperience pro
Active
CE MDR
Valid until
21 Dec 2028
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number84353873xperiencepro2U 08435387314204 | Date6 Jul 2026 | StatusActive |
Certificates
- 2024 DR 0039 Active
Technical documentation EU MDR
- Certifier
- CENTRO NACIONAL DE CERTIFICACION DE PRODUCTOS SANITARIOS 0318
- Issued
- 4 Nov 2024
- Expires
- 21 Dec 2028
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Model / Reference
- xperience pro, BCPR14N150500010
- Primary DI / UDI-DI
- 08435387314204
- Basic UDI-DI
- 84353873xperiencepro2U
- Direct Marketing DI
- 08435387314204
- EMDN Code
- C010402020101 PTA balloon dilatation catheters
- Device Class
- Class III
- EU market of registration
- Spain
Manufacturer details
- EUDAMED SRN
- ES-MF-000019783
Other devices from Life Vascular Devices Biotech, S.L.
Properties
Other properties (12)
- 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
- Measuring Function: No
- Incorporates Medicinal Product: No