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C30-2-Uk (c30-Uk-Ac)

EUDAMED

Class I (EU MDR)

Ref C30-UK-ACModel C30-2-UK

by OMRON Healthcare Co., Ltd.

Identity

Trade Name
C30-2-UK (C30-UK-AC) EUDAMED
Device Name
C30-UK-AC EUDAMED
Model / Reference
C30-2-UK EUDAMED
C30-UK-AC EUDAMED

Identifiers

Primary DI / UDI-DI
04015672112841 EUDAMED
Basic UDI-DI
4015672112845F EUDAMED
EMDN Code
Z129080 VARIOUS INSTRUMENTS FOR FUNCTIONAL EXPLORATION AND THERAPEUTIC INTERVENTIONS - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Northern Ireland 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

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

C30-2-Uk (c30-Uk-Ac) by OMRON Healthcare Co., Ltd. — Class I — 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 694567bb-10d4-4704-bf3a-54931e3df3b2 61 fields · synced Jun 19, 2026