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Genedian

EUDAMED

Class IVD General (EU MDR)

Ref P122-07048

by Hangzhou DIAN Biotechnology Co., Ltd.

Identity

Trade Name
GENEDIAN EUDAMED
Device Name
Cervical Cancer Methylation Test EUDAMED
Model / Reference
P122-07048 EUDAMED

Identifiers

Primary DI / UDI-DI
D-RA013UJ EUDAMED
Basic UDI-DI
B-RA013UJ EUDAMED
EMDN Code
W010699 GENETIC TESTS - 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

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

Genedian by Hangzhou DIAN Biotechnology 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-000007252
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 1124054c-168c-4f6a-9b82-6c1238f95fbf 61 fields · synced Jun 18, 2026