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Fluorescence Immunoassay Analyzer

EUDAMED

Class A (EU MDR)

Ref FluoreMini

by Singuway Biotech Inc.

Identity

Trade Name
Fluorescence Immunoassay Analyzer EUDAMED
Device Name
Fluorescence Immunoassay Analyzer EUDAMED
Model / Reference
FluoreMini EUDAMED

Identifiers

Primary DI / UDI-DI
06974081870736 EUDAMED
Basic UDI-DI
697408187FluoreMiniL4 EUDAMED
Direct Marketing DI
06974081870736 EUDAMED
EMDN Code
W0201020101 AUTOMATED IMMUNOCHEMISTRY ANALYSERS - LOW ROUTINE (Throughput <= 100 test/h) EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Greece 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

Fluorescence Immunoassay Analyzer by Singuway Biotech 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

EUDAMED SRN
CN-MF-000027180
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED dab816d4-acb0-4fc7-8b4b-ab1e79bf02a2 61 fields · synced Jun 18, 2026