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Vision-MR® Dispersive Electrode

EUDAMED

Class I (EU MDR)

Ref VMR300

by Imricor Medical Systems, Inc.

Identity

Trade Name
Vision-MR® Dispersive Electrode EUDAMED
Device Name
Vision-MR® Dispersive Electrode EUDAMED
Model / Reference
VMR300 EUDAMED

Identifiers

Primary DI / UDI-DI
10854277008224 EUDAMED
Basic UDI-DI
0854277008VMR3XXF7 EUDAMED
Unit of Use DI
00854277008227 EUDAMED
EMDN Code
K02010201 ELECTROSURGERY SINGLE PATIENT PADS (NEUTRAL ELECTRODES), SINGLE-USE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

Yes

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

Vision-MR® Dispersive Electrode by Imricor Medical Systems, Inc. — 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
US-MF-000017310
Authorised Representative
MedR-AR Services B.V. NL-AR-000000120

Sources (1)

  • EUDAMED 7776cae3-8696-4b3d-87bf-3dd4f9a089f6 61 fields · synced Jun 20, 2026