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 - Magstim Inc

Address:

78 Centennial Loop Suite C

Eugene

Eugene

Orogen OR 97401

United States

Authorised Representative/ UK Responsible Person
Name: The Magstim Company Limited
Address:

The Magstim Company Limited Spring Gardens

Whitland

Carmarthenshire SA34 0HR

United Kingdom

Code/Term Type

Electroencephalograph Electroencephalograph 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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