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Mumps Virus IgM Ab Rapid Test Kit

EUDAMED

Class IVD General (EU MDR)

Ref GKPD101

by Dezhou Guoke Medical Technology Co., Ltd.

Identity

Trade Name
Mumps Virus IgM Ab Rapid Test Kit EUDAMED
Device Name
Mumps Virus IgM Ab Rapid Test Kit EUDAMED
Model / Reference
GKPD101 EUDAMED

Identifiers

Primary DI / UDI-DI
D-GKPD101WY EUDAMED
Basic UDI-DI
B-GKPD101WY 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

Mumps Virus 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

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Manufacturer

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

Sources (1)

  • EUDAMED 8e447c8a-2aba-4e7c-822e-541e3894688b 61 fields · synced Jun 18, 2026