← Back to catalogue

Follicle-stimulating Hormone Test Kit (FIA)

EUDAMED

Class IVD General (EU MDR)

Ref VID31-05-011Model VID31

by VivaChek Biotech (Hangzhou) Co., Ltd.

Identity

Trade Name
Follicle-stimulating Hormone Test Kit (FIA) EUDAMED
Device Name
Follicle-stimulating Hormone Test Kit (FIA) EUDAMED
Model / Reference
VID31 EUDAMED
VID31-05-011 EUDAMED

Identifiers

Primary DI / UDI-DI
D-VID312S EUDAMED
Basic UDI-DI
B-VID312S EUDAMED
EMDN Code
W0102050104 FOLLICLE STIMULATING HORMONE EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

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

Follicle-stimulating Hormone Test Kit (FIA) by VivaChek Biotech (Hangzhou) Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED

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 (1)

  • EUDAMED fe1a05fb-7f98-4714-b24c-cc7b98101ebd 61 fields · synced Jun 18, 2026