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Samphire Neuroscience Ltd

United Kingdom UK-MF-000036806 Last updated 22 Oct 2026

Devices
1
Registries
EUDAMED
FDA recalls
0

Catalogue1

  • Nettle Ref BAND-100

    Class IIa EUDAMED Active

EUDAMED certificates1

Held under this manufacturer's EUDAMED registration, grouped by notified body; in force first, then by expiry.

EUDAMED certificates (1)

ENTE CERTIFICAZIONE MACCHINE SRL 1282 1 certificate

  • ECM24MDR005 Issued

    Quality management system EU MDR

    Issued
    21 Jun 2024
    Expires
    20 Jun 2029

Authorised representatives

About

Samphire builds advanced brain-based technologies to tackle pain and mood symptoms caused by hormonal change.

From the manufacturer's own website. Source

What Samphire Neuroscience Ltd makes

Samphire Neuroscience Ltd develops neurostimulation devices, including the Nettle system, designed to target pain and mood symptoms associated with hormonal fluctuations. The technology appears to focus on non-invasive or minimally invasive brain modulation for symptom management.

The company’s devices fall under EU Class IIa classification and are registered in the EUDAMED database. Samphire Neuroscience Ltd is based in the United Kingdom.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Samphire Neuroscience Ltd manufacture?

Samphire Neuroscience Ltd specialises in neurostimulation devices, such as the Nettle system. These devices are designed to address pain and mood symptoms linked to hormonal changes, focusing on non-invasive or minimally invasive brain modulation for symptom management.

Where is Samphire Neuroscience Ltd based?

Samphire Neuroscience Ltd is headquartered in the United Kingdom. The company’s location is relevant for regulatory compliance and device registration purposes, particularly within the EU.

Which regulatory registries list Samphire Neuroscience Ltd’s devices?

Samphire Neuroscience Ltd’s devices are registered in the EUDAMED database, which is the European Union’s centralised system for tracking medical devices and their manufacturers. This registry is used for transparency and compliance with EU regulations.

How are Samphire Neuroscience Ltd’s devices classified under EU regulations?

Samphire Neuroscience Ltd’s devices fall under EU Class IIa classification. This classification is determined based on the risk associated with the device’s intended use, with Class IIa indicating moderate risk requiring specific conformity assessment procedures before market placement.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
United Kingdom(from SRN)
Address
167-169, Great Portland Street, London, United Kingdom (ex Northern Ireland)
PRRC contact
Hyun-Woo Cho
EUDAMED SRN
UK-MF-000036806