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Oncology 59-Gene Variant Assay

EUDAMED

Class IVD General (EU MDR)

Ref KB5005048

by Suzhou GenePlus Biomedical Engineering Co., Ltd.

Identity

Trade Name
Oncology 59-Gene Variant Assay EUDAMED
Device Name
Oncology 59-Gene Variant Assay EUDAMED
Model / Reference
KB5005048 EUDAMED

Identifiers

Primary DI / UDI-DI
06975352996032 EUDAMED
Basic UDI-DI
B-06975352996032 EUDAMED
EMDN Code
W010699 GENETIC TESTS - OTHER EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Italy 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

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

Oncology 59-Gene Variant Assay by Suzhou GenePlus Biomedical Engineering 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-000035774
Authorised Representative
RIOMAVIX SOCIEDAD LIMITADA ES-AR-000001202

Sources (1)

  • EUDAMED 85ea974f-a542-4671-b16d-9ef2868318af 61 fields · synced Jun 20, 2026