GoldCath
by Demersan Biyoteknoloji İmalat Sanayi̇ Ve Ti̇caret Anoni̇m Şi̇rketi̇ 18 variants
Ref 2006Model Urinary Nelaton Catheter GN-CH 06-20 CM, Hydrophılıc Urınary Catheter Sheath GKF-CH 06-20 CM, Hydrophilic Urinary Catheter Dilatation GDL-CH 06-20 CM, Hydrophilic Urinary Kit GKT-CH 06-20 CM, Hydrophilic Urinary Catheter Ring GYU-CH 06-20 CM
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-08680110403551 | Date24 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- Withdrawn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
- Device Name
- Urinary Nelaton CatheterHydrophılıc Urınary Catheter SheathHydrophilic Urinary Catheter DilatationHydrophilic Urinary KitHydrophilic Urinary Catheter Ring
- Model / Reference
- Urinary Nelaton Catheter GN-CH 06-20 CM, 2006, Hydrophılıc Urınary Catheter Sheath GKF-CH 06-20 CM, Hydrophilic Urinary Catheter Dilatation GDL-CH 06-20 CM, Hydrophilic Urinary Kit GKT-CH 06-20 CM, Hydrophilic Urinary Catheter Ring GYU-CH 06-20 CM
- Primary DI / UDI-DI
- 08680110403551, 08680110401878, 08680110402554, 08680110400857, 08680110401199
- Basic UDI-DI
- B-08680110403551, B-08680110401878, B-08680110402554, B-08680110400857, B-08680110401199
- EMDN Code
- U01010502, U01010501
- Device Class
- Class IIa
- EU market of registration
- Türkiye
Manufacturer details
- EUDAMED SRN
- TR-MF-000038388
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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