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Cardiette / Cardioline 660 100 26

EUDAMED

Class I (EU MDR)

Ref SK-CA-13025-20BS3Model SKYMED

by Isd Meditech Sdn. Bhd.

Identity

Trade Name
CARDIETTE / CARDIOLINE 660 100 26 EUDAMED
Device Name
Medical Chart Recording Paper EUDAMED
Model / Reference
SKYMED EUDAMED
SK-CA-13025-20BS3 EUDAMED

Identifiers

Primary DI / UDI-DI
09551019812029 EUDAMED
Basic UDI-DI
955101981MCRP-SMPY EUDAMED
Direct Marketing DI
09551019812029 EUDAMED
EMDN Code
Z12050385 ELECTROCARDIOGRAPHS - CONSUMABLES EUDAMED

Classification

Device Class
Class I 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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Electrocardiographic lead set, reusable

Cardiette / Cardioline 660 100 26 by Isd Meditech Sdn. Bhd. — 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

EUDAMED SRN
MY-MF-000043531
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (1)

  • EUDAMED ee6f429e-d3fd-4fd7-8301-811f711ae6ab 61 fields · synced Jun 18, 2026