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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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NeuroNation MED — 3 UDI-DI variants, MDR (Synaptikon GmbH)

MD Atlas
Synaptikon GmbH

Data from EUDAMED, last updated May 23, 2026

NeuroNation MED

426242924NeuroNationMEDL3

3 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: Synaptikon GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426242924NeuroNationMEDL3
Device name: NeuroNation MED
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Special device type: refdata.special-mdr-device-type.software
Version date: May 22, 2023

Manufacturer & authorised representative

Manufacturer

Name: Synaptikon GmbH
SRN: DE-MF-000017748
Country: Germany
Email: regulatory@neuronation.de
Phone: +491792242642

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01H0841YNHD94XK3EXRMCCXRX7

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

NeuroNation MED04262429240023
NeuroNation MED42624292400094
NeuroNation MED04262429240016