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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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Organization name
UDI-DI code
Reference / catalog number

NeuroNation MED — Class I MDR by Synaptikon GmbH

MD Atlas
Synaptikon GmbH

EUDAMED last updated this device on Sep 1, 2025

NeuroNation MED

426242924NeuroNationMEDL3

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Synaptikon GmbH
UDI-DI code: 04262429240023
Reference / catalog number: NeuroNation MED

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Manufacturer information

Organization name: Synaptikon GmbH
SRN: DE-MF-000017748
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: NeuroNation MED
UDI-DI code: 04262429240023
Basic UDI-DI: 426242924NeuroNationMEDL3
Reference / catalog number: NeuroNation MED
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: https://neuronation-med.de/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V92MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

NeuroNation MED426242924NeuroNationMEDL3On the market NeuroNation MED426242924NeuroNationMEDL3On the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.