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 - The Blueprint Design Company Ltd

Address:

Martins Barn Birdham Road

Chichester

West Sussex PO20 7BX

United Kingdom

Authorised Representative/ UK Responsible Person
Name:
Address:

Code/Term Type

Clinical information system web-based application software Class I

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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