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Ne-C810

EUDAMED

Class IIa (EU MDR)

Ref NE-C810-E

by OMRON Healthcare Co., Ltd.

Identity

Trade Name
NE-C810 EUDAMED
Device Name
NE-C810 EUDAMED
Model / Reference
NE-C810-E EUDAMED

Identifiers

Primary DI / UDI-DI
04015672114036 EUDAMED
Basic UDI-DI
4015672114034X EUDAMED
EMDN Code
R060101 COLD NEBULISATION SYSTEMS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Ne-C810 by OMRON Healthcare Co., Ltd. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
JP-MF-000007213
Authorised Representative
OMRON Healthcare Europe B.V. NL-AR-000002683

Sources (1)

  • EUDAMED 6cd5cdae-2948-49cb-acca-5671fb0c1b1f 61 fields · synced Jul 25, 2026