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Dr. Max Pregnancy Test 2in1

EUDAMED

Class IVD devices for self-testing (EU MDR)

Ref ACK21001-S02-018Model Strip

by Core Technology Co., Ltd.

Identity

Trade Name
Dr. Max Pregnancy Test 2in1 EUDAMED
Device Name
HCG Pregnancy Tests EUDAMED
Model / Reference
Strip EUDAMED
ACK21001-S02-018 EUDAMED

Identifiers

Primary DI / UDI-DI
D-ACK21001-S02-018AS EUDAMED
Basic UDI-DI
B-ACK21001-S02-018AS EUDAMED
EMDN Code
W0102160302 HCG - RT & POC EUDAMED

Classification

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

Dr. Max Pregnancy Test 2in1 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 be3e1fc9-da82-49d3-a301-1f22d9230a1c 61 fields · synced Jun 18, 2026