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Multiplex Fluorescence Analyzer

EUDAMED

Class A (EU MDR)

Ref 001Model ICX MFA768A

by iCarbonX IntelliCore (Guangdong) Co., Ltd.

Identity

Device Name
Multiplex Fluorescence Analyzer EUDAMED
Model / Reference
ICX MFA768A EUDAMED
001 EUDAMED

Identifiers

Primary DI / UDI-DI
06976043630013 EUDAMED
Basic UDI-DI
697604363ICXD001Q4 EUDAMED
Direct Marketing DI
06976043630013 EUDAMED
EMDN Code
W0201020201 IMMUNOCHEMISTRY READERS 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

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Multiplex Fluorescence Analyzer by iCarbonX IntelliCore (Guangdong) 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-000045482
Authorised Representative
Kingsmead Service B.V. NL-AR-000002066

Sources (1)

  • EUDAMED 70314511-902e-4cd3-a6b5-0122768526db 61 fields · synced Oct 8, 2026