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ZIKA and Yellow Fever Test

EUDAMED

Class IVD General (EU MDR)

Ref ER-0453-02

by Shanghai Zj Bio-Tech Co., Ltd

Identity

Trade Name
ZIKA and Yellow Fever Test EUDAMED
Device Name
ZIKA and Yellow Fever Test EUDAMED
Model / Reference
ER-0453-02 EUDAMED

Identifiers

Primary DI / UDI-DI
06971042225475 EUDAMED
Basic UDI-DI
B-06971042225475 EUDAMED
EMDN Code
W0105040599 VIROLOGY - NA REAGENTS - OTHER 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

ZIKA and Yellow Fever 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 (1)

  • EUDAMED 16cb65b2-4eb7-402a-8d67-f719f78cf7d4 61 fields · synced Jul 22, 2026