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Hemonitor H1 microcuvette

EUDAMED

Class A (EU MDR)

Ref HMAC050

by GenBody Inc.

Identity

Trade Name
Hemonitor H1 microcuvette EUDAMED
Device Name
Hemonitor H1 microcuvette EUDAMED
Model / Reference
HMAC050 EUDAMED

Identifiers

Primary DI / UDI-DI
08800076701199 EUDAMED
Basic UDI-DI
88000767HMAC050EN EUDAMED
EMDN Code
W0503010203 SAMPLES ANALYSES, PLASTIC CUVETTES EUDAMED

Classification

Device Class
Class A 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

No

EUDAMED

Near-Patient Testing

Yes

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Hemonitor H1 microcuvette by Genbody Inc. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

Manufacturer
GenBody Inc.
EUDAMED SRN
KR-MF-000043626
Authorised Representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Sources (1)

  • EUDAMED 897a0758-8717-4ce5-a7f3-e590a306dac7 61 fields · synced Jun 18, 2026