Identity
- Trade Name
- Genedrive® CYP2C19 ID Kit EUDAMED
- Device Name
- Genedrive® CYP2C19 ID Kit EUDAMED
- Model / Reference
- ID-CYP2C19-10-ES EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05060654860516 EUDAMED
- Basic UDI-DI
- 506065486ID-CYP2C19-0197 EUDAMED
- Unit of Use DI
- 05060654860479 EUDAMED
- EMDN Code
- W0106030101 CYP 450 - INDIVIDUAL TEST EUDAMED
Classification
- Device Class
- Class C EUDAMED
- Market of Registration
- Spain EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
Yes
EUDAMED
Microbial Substances
Yes
EUDAMED
Reagent
Yes
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
Yes
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
New Device
Yes
EUDAMED
Genedrive® CYP2C19 ID Kit by Genedrive Diagnostics Ltd — Class C — IVDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/IVDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 506065486ID-CYP2C19-0197 | Class C | Active |
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Manufacturer
- Manufacturer
- Genedrive Diagnostics Ltd.
- EUDAMED SRN
- GB-MF-000012810
- Authorised Representative
- Advena Limited MT-AR-000000234
Sources (1)
- EUDAMED 43f26e3a-42a7-40c0-ae00-ec37fbf2ff52 61 fields · synced Jun 18, 2026