iVascular Nc xperience
by Life Vascular Devices Biotech, S.L. 88 variants
Ref BCTR14150300020Model NC xperience
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 | Number84353873ncxperienceS5 08435387310107 | Date1 Jul 2026 | StatusActive |
Certificates
- 2025 DR 0049 Active
Technical documentation EU MDR
- Certifier
- CENTRO NACIONAL DE CERTIFICACION DE PRODUCTOS SANITARIOS 0318
- Issued
- 24 Jun 2025
- Expires
- 21 Dec 2028
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Model / Reference
- NC xperience, BCTR14150300020
- Primary DI / UDI-DI
- 08435387310107
- Basic UDI-DI
- 84353873ncxperienceS5
- Direct Marketing DI
- 08435387310107
- 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