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HPV IgM Rapid Test Device

EUDAMED

Class IVD General (EU MDR)

Ref K410216D

by Hangzhou Realy Tech Co., Ltd.

Identity

Trade Name
HPV IgM Rapid Test Device EUDAMED
Model / Reference
K410216D EUDAMED

Identifiers

Primary DI / UDI-DI
06971792053960 EUDAMED
Basic UDI-DI
B-06971792053960 EUDAMED
EMDN Code
W0105041001 HPV ANTIGEN / ANTIBODIES 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

HPV IgM Rapid Test Device by Hangzhou Realy Tech 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-000004716
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED d2d720bd-e133-4048-8f6e-af7ce68ee44a 61 fields · synced Jun 19, 2026