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AMH Assay kit CLIA

EUDAMED

Class IVD General (EU MDR)

Ref SUPM080072Ref SUPM080036

by Shenzhen Superbio Technology Co., Ltd.

Identity

Trade Name
AMH Assay kit CLIA EUDAMED
Device Name
AMH Assay kit CLIA EUDAMED
Model / Reference
SUPM080072 EUDAMED
SUPM080036 EUDAMED

Identifiers

Primary DI / UDI-DI
06974521001027 EUDAMED
06974521001010 EUDAMED
Basic UDI-DI
B-06974521001027 EUDAMED
B-06974521001010 EUDAMED
EMDN Code
W0102050215 ANTI-MULLERIAN HORMONE EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Ireland 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

AMH Assay kit CLIA by Shenzhen Superbio Technology 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-000024149
Authorised Representative
QbD RepS BV BE-AR-000000040

Sources (2)

  • EUDAMED f30125a4-67fe-412a-a46c-8f74bcf9f505 61 fields · synced Jul 26, 2026
  • EUDAMED b70d9ad6-f7c1-4d07-83e9-7e043cde526d 61 fields · synced May 17, 2026