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Be Sure LH Ovulationstest

EUDAMED

Class IVD devices for self-testing (EU MDR)

Ref ACK21003-M07-012Model Midstream

by Core Technology Co., Ltd.

Identity

Trade Name
Be Sure LH Ovulationstest EUDAMED
Device Name
LH Ovulation Tests EUDAMED
Model / Reference
Midstream EUDAMED
ACK21003-M07-012 EUDAMED

Identifiers

Primary DI / UDI-DI
16942468182045 EUDAMED
Basic UDI-DI
B-16942468182045 EUDAMED
EMDN Code
W0102160304 LH - RT & POC EUDAMED

Classification

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

Be Sure LH Ovulationstest 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 8ccc0e2a-0e4e-4f32-9225-69a9955ff42c 61 fields · synced Jun 19, 2026