← Back to catalogue

LH One Step Ovulation Test

EUDAMED

Class IVD devices for self-testing (EU MDR)

Ref LH-101/LH-102/LH-103Model Strip,Cassette,Midstream

by Sejoy Biomedical Co., Ltd.

Identity

Trade Name
LH One Step Ovulation Test EUDAMED
Device Name
LH One Step Ovulation Test EUDAMED
Model / Reference
Strip,Cassette,Midstream EUDAMED
LH-101/LH-102/LH-103 EUDAMED

Identifiers

Primary DI / UDI-DI
06939663984065 EUDAMED
Basic UDI-DI
B-06939663984065 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

Yes

EUDAMED

Professional Testing

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

LH One Step Ovulation Test by Sejoy Biomedical 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
CN-MF-000008447
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 11ab779e-47ca-444c-9774-368e454a3b2d 61 fields · synced Jul 28, 2026