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VenusHPV Test

EUDAMED

Class IVD General (EU MDR)

Ref TD-0523-02-48Ref TD-0523-02-24

by Shanghai Zj Bio-Tech Co., Ltd

Identity

Trade Name
VenusHPV Test EUDAMED
Device Name
VenusHPV Test EUDAMED
Model / Reference
TD-0523-02-48 EUDAMED
TD-0523-02-24 EUDAMED

Identifiers

Primary DI / UDI-DI
06971042225291 EUDAMED
06971042225284 EUDAMED
Basic UDI-DI
B-06971042225291 EUDAMED
B-06971042225284 EUDAMED
EMDN Code
W0105041003 PARTIAL GENOTYPING HIGH-RISK HPV - NA REAGENTS EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
France 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

VenusHPV Test by Shanghai Zj Bio-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-000017861
Authorised Representative
RIOMAVIX SOCIEDAD LIMITADA ES-AR-000001202

Sources (2)

  • EUDAMED f9092bf9-4b10-4064-9688-dbda2ea863f1 61 fields · synced Sep 17, 2026
  • EUDAMED e0645b29-3f1b-4059-ba65-47d91c5f1ade 61 fields · synced May 19, 2026