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Defibrillation electrode

EUDAMED

Class I (EU MDR)

Ref AMD-DD-AF0003-XModel AMD-DD

by Shenzhen Amydi-med Electrics Tech Co., Ltd

Identity

Trade Name
Defibrillation electrode EUDAMED
Device Name
Defibrillation electrode EUDAMED
Model / Reference
AMD-DD EUDAMED
AMD-DD-AF0003-X EUDAMED

Identifiers

Primary DI / UDI-DI
06931377244350 EUDAMED
Basic UDI-DI
69313772819V5 EUDAMED
EMDN Code
C020401 EXTERNAL CARDIOVERSION DEFIBRILLATOR ELECTRODE PADS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Denmark 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

Defibrillation electrode by Shenzhen Amydi-med Electrics Tech 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
CN-MF-000013201
Authorised Representative
Umedwings Netherlands B.V. NL-AR-000000444

Sources (1)

  • EUDAMED b57323ee-face-4a5c-b09e-60d08d568074 61 fields · synced Jun 18, 2026