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Genedrive® CYP2C19 Collection Kit

EUDAMED

Class A (EU MDR)

Ref CK-CYP2C19-10-ES

by Genedrive Diagnostics Ltd.

Identity

Trade Name
Genedrive® CYP2C19 Collection Kit EUDAMED
Device Name
Genedrive® CYP2C19 Collection Kit EUDAMED
Model / Reference
CK-CYP2C19-10-ES EUDAMED

Identifiers

Primary DI / UDI-DI
05060654860783 EUDAMED
Basic UDI-DI
506065486CK-CYP2C19-019L EUDAMED
Unit of Use DI
05060654860745 EUDAMED
EMDN Code
W05019099 SAMPLES COLLECTION DEVICES - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

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 Collection Kit by Genedrive Diagnostics Ltd — Class A — 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 845ffbfd-c120-44ed-9ad9-5461384ae59b 61 fields · synced Jun 18, 2026