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KEYU Fluorescence Immunoassay Analyzer

EUDAMED

Class A (EU MDR)

Ref FI-620

by Zhuhai Keyu Biological Engineering Co., Ltd

Identity

Trade Name
KEYU Fluorescence Immunoassay Analyzer EUDAMED
Device Name
Fluorescent Immunoassay Analyzer EUDAMED
Model / Reference
FI-620 EUDAMED

Identifiers

Primary DI / UDI-DI
06974735361115 EUDAMED
Basic UDI-DI
697473536KUA06PE EUDAMED
EMDN Code
W02010299 IMMUNOCHEMISTRY INSTRUMENTS - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Netherlands 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

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

KEYU Fluorescence Immunoassay Analyzer by Zhuhai Keyu Biological Engineering 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
CN-MF-000023195
Authorised Representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Sources (1)

  • EUDAMED 56408941-33fc-4fe6-86bc-32a76ea11b49 61 fields · synced Jun 18, 2026