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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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SEP-Stimulationsadapter an ISIS… — 5 UDI-DI variants, MDR

MD Atlas
inomed Medizintechnik GmbH

Data from EUDAMED, last updated May 23, 2026

SEP-Stimulationsadapter an ISIS Neurostimulator

42503076IZB02087

5 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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UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01K8AZABYC8F6M02BS5RMR0J2J

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

Grid/TES Stimulation matrix 16 Ch. for ISIS Neurostimulator04250307604692
Grid/TES Stimulation matrix 8 Ch. for ISIS Neurostimulator04250307604685
MEP Stimulation Adaptor for Grid/TES Stimulation matrix04250307604630
SEP Stimulation Adaptor for ISIS Neurostimulator04250307604623
Stimulation Adaptor for ISIS Neurostimulator04250307604647

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42503076IZB02087
Device name: SEP-Stimulationsadapter an ISIS Neurostimulator
Device model: 540501
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 24, 2025

Manufacturer & authorised representative

Manufacturer

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

Variants by status