2, 0 X 220 mm VeniFlow 0.018” PTA Balloon Dilatation Catheter (80 cm)
by Alfatip Ki̇mya Kozmeti̇k Tibbi̇ Malz. San. Ve Ti̇c. Ltd. Şti̇.
Ref VFL18200220-80Model Percutaneous Transluminal Angıoplasty (PTA) Dilatation Catheters
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-08683851832901 08683851832901 | Date13 May 2026 | 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- Withdrawn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
- Percutaneous Transluminal Angıoplasty (PTA) Dilatation Catheters, VFL18200220-80
- Primary DI / UDI-DI
- 08683851832901
- Basic UDI-DI
- B-08683851832901
- EMDN Code
- C010402020101 PTA balloon dilatation catheters
- Device Class
- Class IIa
- EU market of registration
- Türkiye
Manufacturer details
- EUDAMED SRN
- TR-MF-000040075
Other devices from Alfatip Ki̇mya Kozmeti̇k Tibbi̇ Malz. San. Ve Ti̇c. Ltd. Şti̇.
See all devices from Alfatip Ki̇mya Kozmeti̇k Tibbi̇ Malz. San. Ve Ti̇c. Ltd. Şti̇. →
Properties
Other properties (10)
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No