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Baby Fast Test ciazowy

EUDAMED

Class IVD devices for self-testing (EU MDR)

Ref ACK21001-M01-014Model Midstream

by Core Technology Co., Ltd.

Identity

Trade Name
Baby Fast Test ciazowy EUDAMED
Device Name
HCG Pregnancy Tests EUDAMED
Model / Reference
Midstream EUDAMED
ACK21001-M01-014 EUDAMED

Identifiers

Primary DI / UDI-DI
06942468134894 EUDAMED
Basic UDI-DI
B-06942468134894 EUDAMED
EMDN Code
W0102160302 HCG - RT & POC EUDAMED

Classification

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

Baby Fast Test ciazowy 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 42eb77e8-63af-45bc-9efd-5715ee8edf57 61 fields · synced Aug 2, 2026