← Back to catalogue

HAV IgG/IgM Rapid Test

EUDAMED

Class IVD General (EU MDR)

Ref VIHA-402Model VIHA

by VivaChek Biotech (Hangzhou) Co., Ltd.

Identity

Trade Name
HAV IgG/IgM Rapid Test EUDAMED
Device Name
HAV IgG/IgM Rapid Test EUDAMED
Model / Reference
VIHA EUDAMED
VIHA-402 EUDAMED

Identifiers

Primary DI / UDI-DI
06937339202260 EUDAMED
06937339209504 EUDAMED
Basic UDI-DI
B-06937339202260 EUDAMED
B-06937339209504 EUDAMED
EMDN Code
W0105090299 HEPATITIS VIRUSES - RT & POC - OTHER EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Netherlands EUDAMED
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMEDEUDAMED

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

HAV IgG/IgM Rapid Test by VivaChek Biotech (Hangzhou) 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000012160
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (2)

  • EUDAMED d764d10c-05b1-43b8-8068-78ea8e17e955 61 fields · synced Oct 7, 2026
  • EUDAMED 01551a1a-6f88-467e-bf17-b12bda3cd7f2 61 fields · synced Oct 6, 2026