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Hemolynac 510-Mk-510wh

EUDAMED

Class A (EU MDR)

Ref MK-510WH

by Nihon Kohden India Private Limited

Identity

Trade Name
HEMOLYNAC 510-MK-510WH EUDAMED
Device Name
Lysing Reagent EUDAMED
Model / Reference
MK-510WH EUDAMED

Identifiers

Primary DI / UDI-DI
08908022609046 EUDAMED
Basic UDI-DI
8908022609IVD0049W EUDAMED
Direct Marketing DI
08908022609046 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

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Hemolynac 510-Mk-510wh by Nihon Kohden India Private Limited — 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
IN-MF-000045419
Authorised Representative
NIHON KOHDEN EUROPE GmbH DE-AR-000010740

Sources (1)

  • EUDAMED febafe5a-beac-4648-a012-7fd429500e0f 61 fields · synced Sep 30, 2026