Yukon Choice Flex
by Translumina Therapeutics Private Limited 7 variants
Ref YCFX4040Model Sirolimus Eluting Coronary Stent System-L605 Cobalt Chromium (40 x 4.00 mm)
Active
CE MDD
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD | NumberB-08904271663679 08904271663679 | Date28 Oct 2025 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDD Active
Specification
- Model / Reference
- Sirolimus Eluting Coronary Stent System-L605 Cobalt Chromium (40 x 4.00 mm), YCFX4040
- Primary DI / UDI-DI
- 08904271663679
- Basic UDI-DI
- B-08904271663679
- EMDN Code
- P070402010301 Coronary drug eluting stents (des) with polymers
- Device Class
- Class III
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- IN-MF-000047911
- Authorised representative
- CMC Medical Devices & Drugs SL ES-AR-000000293
Other devices from Translumina Therapeutics Private Limited
See all devices from Translumina Therapeutics Private Limited →
Properties
Other properties (7)
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Measuring Function: No