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AMH Assay Kit (Fluorescence Immunoassay)

EUDAMED

Class IVD General (EU MDR)

Ref AMH Assay Kit (Fluorescence Immunoassay)Model 20Tests/Kit

by DiYaLab ZJG Biotech Co., Ltd

Identity

Trade Name
AMH Assay Kit (Fluorescence Immunoassay) EUDAMED
Device Name
AMH Assay Kit (Fluorescence Immunoassay) EUDAMED
Model / Reference
20Tests/Kit EUDAMED
AMH Assay Kit (Fluorescence Immunoassay) EUDAMED

Identifiers

Primary DI / UDI-DI
06975424223400 EUDAMED
Basic UDI-DI
B-06975424223400 EUDAMED
EMDN Code
W0102050215 ANTI-MULLERIAN HORMONE EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Austria 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

AMH Assay Kit (Fluorescence Immunoassay) by DiYaLab ZJG Biotech 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-000048648
Authorised Representative
SUNGO Europe B.V. NL-AR-000000247

Sources (1)

  • EUDAMED 64bacbc1-9439-4e8e-b9ed-016058ec2e7d 61 fields · synced Jun 19, 2026