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Fluorocell WNR

EUDAMED

Class A (EU MDR)

Ref CP-066-715

by Sysmex Corporation

Identity

Trade Name
Fluorocell WNR EUDAMED
Device Name
Fluorocell WNR EUDAMED
Model / Reference
CP-066-715 EUDAMED

Identifiers

Primary DI / UDI-DI
14987562509017 EUDAMED
Basic UDI-DI
4987562FLUOROCELLWNRY4 EUDAMED
EMDN Code
W0103010103 COMPLETE CELL COUNT 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

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Fluorocell WNR by Sysmex Corporation — 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
Sysmex Corporation
EUDAMED SRN
JP-MF-000014037
Authorised Representative
Sysmex Europe SE DE-AR-000022333

Sources (1)

  • EUDAMED 65a9a230-1286-4187-98e7-860a04b11c32 61 fields · synced Jul 29, 2026