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Clairivo Menopauze zelftest

EUDAMED

Class IVD devices for self-testing (EU MDR)

Ref ACK21005-M01-002Model Midstream

by Core Technology Co., Ltd.

Identity

Trade Name
Clairivo Menopauze zelftest EUDAMED
Device Name
FSH Tests for Self-testing EUDAMED
Model / Reference
Midstream EUDAMED
ACK21005-M01-002 EUDAMED

Identifiers

Primary DI / UDI-DI
06942468170748 EUDAMED
Basic UDI-DI
B-06942468170748 EUDAMED
EMDN Code
W0102160301 FSH - RT & POC EUDAMED

Classification

Device Class
Class IVD devices for self-testing EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

Yes

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

Clairivo Menopauze zelftest by Core Technology Co., Ltd. — Class IVD devices for self-testing — 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-000023522
Authorised Representative
Wellkang Ltd XI-AR-000001836

Sources (1)

  • EUDAMED cd9b7e8f-395b-4955-b5ec-f8cfd16b5d8c 61 fields · synced Jun 20, 2026