Nelaton Catheter Female 8Ch
by Türev İç Ve Diş Ti̇c. Anoni̇m Şi̇rketi̇
Ref 104 0802 1
Active
CE MDR
Valid until
7 May 2030
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number2975-MED-2512801 | Date8 May 2025 | StatusActive |
Certificates
- 2975-MED-2512801 Active
Quality management system EU MDR
- Certifier
- SZUTEST Konformitätsbewertungsstelle GmbH 2975
- Issued
- 8 May 2025
- Expires
- 7 May 2030
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Nelaton Catheter
- Model / Reference
- 104 0802 1
- Primary DI / UDI-DI
- 08682241350568
- Basic UDI-DI
- 868224135TF05-N-BC
- Direct Marketing DI
- 08682241350568
- EMDN Code
- U01010502 Nelaton catheters, non self-lubricating
- Device Class
- Class IIa
- EU market of registration
- Türkiye
Manufacturer details
- EUDAMED SRN
- TR-MF-000039871
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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