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iGFBP-1 Rapid Test

EUDAMED

Class IVD General (EU MDR)

Ref VHIG-702Model VHIG

by VivaChek Biotech (Hangzhou) Co., Ltd.

Identity

Trade Name
iGFBP-1 Rapid Test EUDAMED
Device Name
iGFBP-1 Rapid Test EUDAMED
Model / Reference
VHIG-702 EUDAMED
VHIG EUDAMED

Identifiers

Primary DI / UDI-DI
D-VHIG-702MK EUDAMED
06937339209894 EUDAMED
Basic UDI-DI
B-VHIG-702MK EUDAMED
B-06937339209894 EUDAMED
EMDN Code
W0102160399 FERTILITY/PREGNANCY 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

iGFBP-1 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

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Manufacturer

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

Sources (2)

  • EUDAMED 9fa77092-af6d-4d97-98c7-53612e453b26 61 fields · synced Oct 6, 2026
  • EUDAMED 7ab94232-9a02-4035-82bd-6a6e1fbe3229 61 fields · synced Jul 27, 2026