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Menopause

EUDAMED

Class IVD devices for self-testing (EU MDR)

Ref 300220

by Hangzhou Alltest Biotech.Co., Ltd.

Identity

Device Name
Menopause EUDAMED
Model / Reference
300220 EUDAMED

Identifiers

Primary DI / UDI-DI
D-300220LE EUDAMED
Basic UDI-DI
B-300220LE EUDAMED
EMDN Code
W0102160301 FSH - 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

Menopause by Hangzhou Alltest Biotech.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-000010710
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED 5abeaf27-68e8-4c4d-974f-60522e82f0a6 61 fields · synced Jun 19, 2026