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Hemolynac・3N MEK-680

EUDAMED

Class A (EU MDR)

Ref T497

by Nihon Kohden Corporation

Identity

Trade Name
Hemolynac・3N MEK-680 EUDAMED
Device Name
CBC-REAGENTS (CLEANING-/DILUTING-/LYSING-/SHEAT-FLUIDS) EUDAMED
Model / Reference
T497 EUDAMED

Identifiers

Primary DI / UDI-DI
04931921867471 EUDAMED
Basic UDI-DI
4931921IVD0017P2 EUDAMED
EMDN Code
W0103010105 CBC-REAGENTS (CLEANING-/DILUTING-/LYSING-/SHEATH-FLUIDS) 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

Hemolynac・3N MEK-680 by Nihon Kohden 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

EUDAMED SRN
JP-MF-000019022
Authorised Representative
NIHON KOHDEN EUROPE GmbH DE-AR-000010740

Sources (1)

  • EUDAMED 98955663-d651-4ce9-bc1b-d59e67d3f63e 61 fields · synced Jul 9, 2026