Alvision
by Alvimedica Tibbi Urunler San. ve Dis Tic. A.S. 207 variants
Ref 501110188804
Active
CE MDR
Valid until
3 Jul 2028
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number086991955Alvision5D 08699195508211 | Date27 Mar 2025 | StatusActive |
Certificates
- 0425-MDR-006770-00 Active
Technical documentation EU MDR
- Certifier
- ICIM S.P.A. 0425
- Issued
- 4 Jul 2023
- Expires
- 3 Jul 2028
- 0425-MDR-006771-00 Active
Quality management system EU MDR
- Certifier
- ICIM S.P.A. 0425
- Issued
- 4 Jul 2023
- Expires
- 3 Jul 2028
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Alvision Interventional Cardiology Diagnostic Catheter
- Model / Reference
- 501110188804
- Primary DI / UDI-DI
- 08699195508211
- Basic UDI-DI
- 086991955Alvision5D
- Direct Marketing DI
- 08699195508211
- EMDN Code
- C0104010101 Cardiac angiography diagnostic catheters
- Device Class
- Class III
- EU market of registration
- Türkiye
Manufacturer details
- EUDAMED SRN
- TR-MF-000029915
Other devices from Alvimedica Tibbi Urunler San. ve Dis Tic. A.S.
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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