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 - Elekta Inc.

Address:

100 Mathilda Place Fifth Floor

Sunnyvale

California 94086

United States

Authorised Representative/ UK Responsible Person
Name: Elekta Ltd
Address:

Cornerstone London Road

Crawley

West Sussex RH10 9BL

United Kingdom

Code/Term Type

Patient health record information system application software Patient health record information system application software Class IIb

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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