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Hemolynac 5-Mek-910h

EUDAMED

Class A (EU MDR)

Ref MEK-910H

by Nihon Kohden India Private Limited

Identity

Trade Name
HEMOLYNAC 5-MEK-910H EUDAMED
Device Name
Lysing Reagent EUDAMED
Model / Reference
MEK-910H EUDAMED

Identifiers

Primary DI / UDI-DI
08908022609022 EUDAMED
Basic UDI-DI
8908022609IVD0049W EUDAMED
Direct Marketing DI
08908022609022 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 5-Mek-910h 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 34514041-8ca0-4f31-8953-c939ec43d5bf 61 fields · synced Aug 4, 2026