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Lynorhag

EUDAMED

Class A (EU MDR)

Ref CL-485-270

by Sysmex Corporation

Identity

Device Name
LYNORHAG EUDAMED
Model / Reference
CL-485-270 EUDAMED

Identifiers

Primary DI / UDI-DI
04987562412730 EUDAMED
Basic UDI-DI
4987562LYNORHAGZ2 EUDAMED
EMDN Code
W02050185 NUCLEIC ACID TESTING INSTRUMENTS EXCEPT MICRO-ARRAYS - CONSUMABLES 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

Lynorhag 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 40db89fb-b4d1-4eca-bc2b-2d20865969af 61 fields · synced Jul 13, 2026