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

Back to MHRA

Manufacturer's Devices - ScandiDos AB

Address:

Uppsala Science Park

Uppsala

SE-751 83

Sweden

Authorised Representative/ UK Responsible Person
Name: Oncology Imaging Systems Ltd
Address:

Carriers Way East Hoathly

Lewes

East Sussex BN8 6AG

England United Kingdom

Code/Term Type

Accelerator system quality assurance device Accelerator system quality assurance device Class IIb

Multi-modality therapeutic radiation phantom anthropomorphic Multi-modality therapeutic radiation phantom anthropomorphic Class I

Contact details

Freedom of information

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

© 2011 Crown Copyright. To contact us about this website, use our feedback form.

Code/Term		Type
Accelerator system quality assurance device	Accelerator system quality assurance device	Class IIb
Multi-modality therapeutic radiation phantom anthropomorphic	Multi-modality therapeutic radiation phantom anthropomorphic	Class I