Vidi Medikal Teknik
by Vİdi̇ Medi̇kal Tekni̇k Veysel Özkapici Ve Kurtuluş Özkapici Kollekti̇f Şi̇rketi̇ 72 variants
Ref C-190Model Backflush Instrument 23G Passive Aspiration
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-08683318131905 08683318131905 | Date21 Aug 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- Withdrawn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
- Device Name
- Backflush Instrument 23G Passive Aspiration
- Model / Reference
- Backflush Instrument 23G Passive Aspiration, C-190
- Primary DI / UDI-DI
- 08683318131905
- Basic UDI-DI
- B-08683318131905
- EMDN Code
- Q021199 Ophthalmic surgery instruments, single-use - other
- Device Class
- Class IIa
- EU market of registration
- Italy
Manufacturer details
- EUDAMED SRN
- TR-MF-000027806
Other devices from Vİdi̇ Medi̇kal Tekni̇k Veysel Özkapici Ve Kurtuluş Özkapici Kollekti̇f Şi̇rketi̇
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