KONIX - Y0000.101.0011 - NON-STERILE ULTRASOUND GEL - 5000 ml
by Turkuaz Sağlik Hi̇zmetleri̇ Medi̇kal Temi̇zli̇k Ki̇myasal Ürünler Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇ 31 variants
Ref 251003Model Y0000.101.0011
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number868171534101J8 08683229604147 | Date18 Feb 2026 | StatusActive |
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- KONIX - Y0000.101.0011 - NON-STERILE ULTRASOUND GEL - 5000 ml
- Model / Reference
- Y0000.101.0011, 251003
- Primary DI / UDI-DI
- 08683229604147
- Basic UDI-DI
- 868171534101J8
- Direct Marketing DI
- 08683229604147
- EMDN Code
- Z1399 Non-specific consumables for diagnostic instruments - other
- Device Class
- Class I
- EU market of registration
- France
Manufacturer details
- EUDAMED SRN
- TR-MF-000015402
Other devices from Turkuaz Sağlik Hi̇zmetleri̇ Medi̇kal Temi̇zli̇k Ki̇myasal Ürünler Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇
Properties
Other properties (13)
- Sterile: No
- 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