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Tinnitus therapy auditory/translingual electrical stimulation system - UK MHRA Medical Device Registration

Tinnitus therapy auditory/translingual electrical stimulation system is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 103734. The device is manufactured by Neuromod Devices Limited from Ireland, classified as General Medical Device. The authorized representative in the UK is Compliant Medical Devices Ltd.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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Tinnitus therapy auditory/translingual electrical stimulation system
MHRA Device ID: 103734โ€ขRef: 103734

Device Type

General Medical Device

Devices

Tinnitus therapy auditory/translingual electrical stimulation system

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Aug 27, 2024

Manufacturer Information

Address

Rainsford Street

Dublin, Ireland

Created Date

Sep 12, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

The Chapel

Whitchurch, Hampshire, England, United Kingdom

Postcode: RG28 7LN

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