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Kenz Suzuken P210x60z-Dm3

EUDAMED

Class I (EU MDR)

Ref SK-K210300-200RS3Model SKYMED

by Isd Meditech Sdn. Bhd.

Identity

Trade Name
KENZ SUZUKEN P210X60Z-DM3 EUDAMED
Device Name
Medical Chart Recording Paper EUDAMED
Model / Reference
SKYMED EUDAMED
SK-K210300-200RS3 EUDAMED

Identifiers

Primary DI / UDI-DI
09551019815617 EUDAMED
Basic UDI-DI
955101981MCRP-SMPY EUDAMED
Direct Marketing DI
09551019815617 EUDAMED
EMDN Code
Z12059009 ECG DATA MANAGEMENT SYSTEMS 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

Kenz Suzuken P210x60z-Dm3 by Isd Meditech Sdn. Bhd. — 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
MY-MF-000043531
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (1)

  • EUDAMED f9f15c8b-c410-45c6-8531-687587ea13bc 61 fields · synced Jul 12, 2026