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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

epihunter-3.0 — Class I MDR by farow

MD Atlas
farow

EUDAMED last updated this device on Mar 31, 2026

epihunter-3.0

5430005150epihunter3-LC

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: farow
UDI-DI code: 05430005150007
Reference / catalog number: epihunter-3.0

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Manufacturer information

Organization name: farow
SRN: BE-MF-000043624
Manufacturer status: Active

Market distribution

Primary placement in Belgium; available across 2 countries total.

Country	On market since	Until
BelgiumPrimary placement		Still on market
Netherlands		Still on market

Device identification

Trade name: not provided
UDI-DI code: 05430005150007
Basic UDI-DI: 5430005150epihunter3-LC
Reference / catalog number: epihunter-3.0
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: epihunter 3.0 is an artificial intelligence based software solution that analyses EEG data from a consumer grade EEG headset to automatically detect absence seizures. Upon seizure detection, the event is signaled to the people around (via light/sound) and the event is logged in an automated electronic seizure diary. Optionally, a video is automatically recorded, including a short period before seizure onset and after the seizure has ended. The person with (suspected) absence seizures or their caregivers can add extra information.
Additional information URL: https://www.epihunter.com/ifu
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12109092VARIOUS NEUROLOGY AND NEUROSURGERY INSTRUMENTS - MEDICAL DEVICE SOFTWARE

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

This device is not currently linked to any other device.

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.