← Back to catalogue

Nipah Virus IgG/IgM Ab Rapid Test Kit

EUDAMED

Class IVD General (EU MDR)

Ref GKPD113

by Dezhou Guoke Medical Technology Co., Ltd.

Identity

Trade Name
Nipah Virus IgG/IgM Ab Rapid Test Kit EUDAMED
Device Name
Nipah Virus IgG/IgM Ab Rapid Test Kit EUDAMED
Model / Reference
GKPD113 EUDAMED

Identifiers

Primary DI / UDI-DI
D-GKPD113X7 EUDAMED
Basic UDI-DI
B-GKPD113X7 EUDAMED
EMDN Code
W0105099099 VIROLOGY - RT & POC - OTHER EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

Nipah Virus IgG/IgM Ab Rapid Test Kit by Dezhou Guoke Medical Technology Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000044128
Authorised Representative
MedPath GmbH DE-AR-000000087

Sources (1)

  • EUDAMED 32961290-9180-461b-8433-769572e5c094 61 fields · synced Jun 19, 2026