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SB Cuvette II

EUDAMED

Class A (EU MDR)

Ref CM500820

by Sysmex Corporation

Identity

Device Name
SB Cuvette II EUDAMED
Model / Reference
CM500820 EUDAMED

Identifiers

Primary DI / UDI-DI
04987562499748 EUDAMED
Basic UDI-DI
4987562SBCuvetteIIM4 EUDAMED
EMDN Code
W0503010203 SAMPLES ANALYSES, PLASTIC CUVETTES 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

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

SB Cuvette II 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 d26f2f2f-637d-4a74-97fb-5e4441adbc2c 61 fields · synced Jun 19, 2026