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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Kabel für TC-Elektroden an S&N… — 8 UDI-DI variants, MDR

MD Atlas
inomed Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

Kabel für TC-Elektroden an S&N Electrothermal, SuperLight

42503076PZR020EJ

8 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: inomed Medizintechnik GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42503076PZR020EJ
Device name: Kabel für TC-Elektroden an S&N Electrothermal, SuperLight
Device model: 260060
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 28, 2025

Manufacturer & authorised representative

Manufacturer

Name: inomed Medizintechnik GmbH
SRN: DE-MF-000005589
Country: Germany
Email: info@inomed.com
Phone: +49764194140

Variants by status

UDI-DI variants

8 UDI-DI variants

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Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

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Intermediate Cable for use with Lisiject at LG204250307609864
sEEG-Box for LG2-sEEG 1 channel sEEG power controlled04250307610617