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Genedrive® CYP2C19 ID Kit

EUDAMED

Class C (EU MDR)

Ref ID-CYP2C19-10-TR

by Genedrive Diagnostics Ltd.

Identity

Trade Name
Genedrive® CYP2C19 ID Kit EUDAMED
Device Name
Genedrive® CYP2C19 ID Kit EUDAMED
Model / Reference
ID-CYP2C19-10-TR EUDAMED

Identifiers

Primary DI / UDI-DI
05060654860561 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
Türkiye 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

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Manufacturer

EUDAMED SRN
GB-MF-000012810
Authorised Representative
Advena Limited MT-AR-000000234

Sources (1)

  • EUDAMED 555e554a-bbb0-437a-b6cf-eef12cfbef68 61 fields · synced Jun 18, 2026