Public Access Database for Medical Device Registration

Registration does not represent any form of accreditation, certification or approval by the UK Competent Authority(MHRA)
Where a conformity assessment certificate is listed as expired, existing products already placed on the market prior to the expiry may not be affected by this expiry and can continue to be used. This expiry stops new products being placed on the market until there is a new certificate of conformity

Manufacturer's By Name

By Device

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Manufacturer's Devices - Neuromod Devices Limited

Address:

Rainsford Street

Dublin

D08 R2YP

Ireland

Authorised Representative/ UK Responsible Person
Name: Compliant Medical Devices Ltd
Address:

The Chapel

Whitchurch

Hampshire RG28 7LN

England United Kingdom

Code/Term Type

Tinnitus therapy auditory/translingual electrical stimulation system Tinnitus therapy auditory/translingual electrical stimulation system Class IIa

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

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