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 - EURORAD SA

Address:

2 RUE ETTORE BUGATTI

ECKBOLSHEIM

67201

France

Authorised Representative/ UK Responsible Person
Name: Bright Technologies Ltd
Address:

Unit 1 Holbrook Commerce Park Holbrook Close Holbrook Industrial Estate Holbrook

Sheffield

South Yorkshire S20 3FJ

United Kingdom

Code/Term Type

Hand-held-detector nuclear medicine system Hand-held-detector nuclear medicine 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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