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LH Ovulation Rapid Test

EUDAMED

Class IVD devices for self-testing (EU MDR)

Ref GALH-103b-7T

by Zhejiang Orient Gene Biotech Co., Ltd

Identity

Trade Name
LH Ovulation Rapid Test EUDAMED
Device Name
LH Ovulation Rapid Test EUDAMED
Model / Reference
GALH-103b-7T EUDAMED

Identifiers

Primary DI / UDI-DI
D-GALH-103b-7TG9 EUDAMED
Basic UDI-DI
B-GALH-103b-7TG9 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

Yes

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

Yes

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

LH Ovulation Rapid Test by Zhejiang Orient Gene Biotech Co., Ltd — Class IVD devices for self-testing — CE/MDR — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000017965
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED 115d9346-9b18-4466-8657-e2245b6d14b5 61 fields · synced Oct 6, 2026