BioMC Coronary Microcatheter
by Biosensors Europe SA 2 variants
Ref MC1-150Model MC1-135
Active
CE MDR
Valid until
1 Nov 2029
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number8888893MC1RR 08888893032702 | Date5 May 2026 | StatusActive |
Certificates
- 2274451TD03 Active
Technical documentation EU MDR
- Certifier
- DEKRA Certification B.V. 0344
- Issued
- 7 Dec 2024
- Expires
- 1 Dec 2029
- 2274451CE01 Active
Quality management system EU MDR
- Certifier
- DEKRA Certification B.V. 0344
- Issued
- 2 Apr 2026
- Expires
- 1 Nov 2029
- Reason
- Add device or group
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Model / Reference
- MC1-135, MC1-150
- Primary DI / UDI-DI
- 08888893032702
- Basic UDI-DI
- 8888893MC1RR
- EMDN Code
- C01040199 Cardiac angiography devices - other
- Device Class
- Class III
- EU market of registration
- Netherlands
Manufacturer details
- EUDAMED SRN
- CH-MF-000015764
- Authorised representative
- NVT GmbH DE-AR-000006441
Other devices from Biosensors Europe SA
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