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Standard 10-lead Patient Cable IEC

EUDAMED

Class I (EU MDR)

Ref 989803184921Model Lead Set/Patient Cable/Lead Upgrade Kit

by Philips Medizin Systeme Böblingen GmbH

Identity

Trade Name
Standard 10-lead Patient Cable IEC EUDAMED
Device Name
Lead Set/Patient Cable/Lead Upgrade Kit EUDAMED
Model / Reference
Lead Set/Patient Cable/Lead Upgrade Kit EUDAMED
989803184921 EUDAMED

Identifiers

Primary DI / UDI-DI
00884838117358 EUDAMED
Basic UDI-DI
0884838BM1861N5 EUDAMED
EMDN Code
Z12050380 ELECTROCARDIOGRAPHS - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria 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

Standard 10-lead Patient Cable IEC by Philips Medizin Systeme Böblingen GmbH — 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
DE-MF-000006026

Sources (1)

  • EUDAMED 037242ac-a4a2-4e58-9e2f-fa67d2c131e0 61 fields · synced Jun 18, 2026