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Patient cable 13 wires for HD+

EUDAMED

Class I (EU MDR)

Ref 63050118Ref 63050131Ref 63050161Ref 63050133

by CARDIOLINE SpA

Identity

Device Name
Patient cable 13 wires for HD+ EUDAMED
Model / Reference
63050118 EUDAMED
63050131 EUDAMED
63050161 EUDAMED
63050133 EUDAMED

Identifiers

Primary DI / UDI-DI
08056732652750 EUDAMED
08056732652781 EUDAMED
08056732653375 EUDAMED
08056732652798 EUDAMED
Basic UDI-DI
0805673265024000016M EUDAMED
Direct Marketing DI
08056732652750 EUDAMED
08056732652781 EUDAMED
08056732653375 EUDAMED
08056732652798 EUDAMED
EMDN Code
Z12050380 ELECTROCARDIOGRAPHS - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy 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

Category: Electrocardiographic lead set, reusable

Patient cable 13 wires for HD+ by Cardioline Spa — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Electrocardiographic lead set, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
CARDIOLINE SpA
EUDAMED SRN
IT-MF-000029682

Sources (4)

  • EUDAMED 7bf9ea67-6a30-4ccb-8222-19c1e8f04048 61 fields · synced Aug 1, 2026
  • EUDAMED 9e7cb4ad-4909-4505-ab01-6549895d9cf1 61 fields · synced May 17, 2026
  • EUDAMED 3e4f8d4e-29f9-44ab-8804-df6e07fdb60c 61 fields · synced May 18, 2026
  • EUDAMED 8f14defa-b629-4370-84be-bb32776d24d2 61 fields · synced May 19, 2026