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Elektrody do defibrylacji

EUDAMED

Class I (EU MDR)

Ref A-I-NK-120-01

by SORIMEX sp. z o.o.

Identity

Trade Name
Elektrody do defibrylacji EUDAMED
Device Name
Elektrody do defibrylacji EUDAMED
Model / Reference
A-I-NK-120-01 EUDAMED

Identifiers

Primary DI / UDI-DI
05903002216620 EUDAMED
Basic UDI-DI
59030022252466 EUDAMED
EMDN Code
C020401 EXTERNAL CARDIOVERSION DEFIBRILLATOR ELECTRODE PADS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Poland 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

Elektrody do defibrylacji by SORIMEX sp. z o.o. — 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

Manufacturer
SORIMEX sp. z o.o.
EUDAMED SRN
PL-MF-000020958

Sources (1)

  • EUDAMED 52f58aa0-35e1-467f-8c6a-4bbd4509de50 61 fields · synced Oct 6, 2026