Identity
- Trade Name
- Trojcestný kohout – červený NO PVC M EUDAMED
- Device Name
- Trojcestný kohout EUDAMED
- Model / Reference
- V696434-M EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08593540515285 EUDAMED
- Basic UDI-DI
- 85935406TF30TROJKOHOUTYAX EUDAMED
- EMDN Code
- A0703 STOPCOCKS EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Czechia EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
Yes
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Trojcestný kohout – červený NO PVC M by GAMA GROUP a.s. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 85935406TF30TROJKOHOUTYAX | Class IIa | Active |
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Manufacturer
- Manufacturer
- GAMA GROUP a.s.
- EUDAMED SRN
- CZ-MF-000011894
Sources (1)
- EUDAMED 9f91af79-38c7-4e16-8ac5-fa6975bbad17 61 fields · synced Jul 19, 2026