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IFVA H3 H1N1 & IFVB Test

EUDAMED

Class IVD General (EU MDR)

Ref RR-0313-02

by Shanghai Zj Bio-Tech Co., Ltd

Identity

Trade Name
IFVA H3 H1N1 & IFVB Test EUDAMED
Device Name
IFVA H3 H1N1 & IFVB Test EUDAMED
Model / Reference
RR-0313-02 EUDAMED

Identifiers

Primary DI / UDI-DI
06971042225420 EUDAMED
Basic UDI-DI
B-06971042225420 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

IFVA H3 H1N1 & IFVB 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 69005685-7ba2-466e-87c5-37a11be54340 61 fields · synced Jun 18, 2026