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Gel Pad S

EUDAMED

Class I (EU MDR)

Ref L-05E

by Nemoto Kyorindo Co., Ltd.

Identity

Trade Name
Gel Pad S EUDAMED
Device Name
Gel Pad S EUDAMED
Model / Reference
L-05E EUDAMED

Identifiers

Primary DI / UDI-DI
14560138482701 EUDAMED
Basic UDI-DI
456013848270AS EUDAMED
EMDN Code
Z11039085 VARIOUS RADIODIAGNOSTIC AND INTERVENTIONAL INSTRUMENTS - CONSUMABLES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Belgium 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

Gel Pad S by Nemoto Kyorindo 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-000004827
Authorised Representative
Medicor International NV/SA BE-AR-000003308

Sources (1)

  • EUDAMED c5792fcf-baaa-4a25-bb58-0574a56297b7 61 fields · synced Jul 26, 2026