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1199100300

EUDAMED

Class A (EU MDR)

Ref 1199100300Model UF-150 / UF-150E / F-150

by Genesystem Co., Ltd.

Identity

Model / Reference
UF-150 / UF-150E / F-150 EUDAMED
1199100300 EUDAMED

Identifiers

Primary DI / UDI-DI
08800118510215 EUDAMED
Basic UDI-DI
88001185HS0010203K EUDAMED
Direct Marketing DI
08800118510215 EUDAMED
EMDN Code
W02050116 NUCLEIC ACID TESTING INTEGRATED EXTRACTION /AMPLIFICATION /DETECTION SYSTEMS EUDAMED

Classification

Device Class
Class A EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

1199100300 by Genesystem Co., Ltd. — 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

EUDAMED SRN
KR-MF-000022998
Authorised Representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Sources (1)

  • EUDAMED cf16c687-26b3-4730-bfd0-a9db26ac388e 61 fields · synced Jul 13, 2026