Samphire Neuroscience Ltd
United Kingdom UK-MF-000036806 Last updated 22 Oct 2026
- Devices
- 1
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Nettle Ref BAND-100
EUDAMED certificates
ENTE CERTIFICAZIONE MACCHINE SRL 1282 1 certificate
- ECM24MDR005 Issued
Quality management system EU MDR
- Issued
- 21 Jun 2024
- Expires
- 20 Jun 2029
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Authorised representatives
Notified bodies
About
Samphire builds advanced brain-based technologies to tackle pain and mood symptoms caused by hormonal change.
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.
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.
Information
- Country
- United Kingdom
- Address
- 167-169, Great Portland Street, London, United Kingdom (ex Northern Ireland)
- Website
- www.samphireneuro.com
- facebook.com/samphireneuro
- [email protected]
- PRRC contact
- Hyun-Woo Cho
- EUDAMED SRN
- UK-MF-000036806