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 - Philips Oy

Address:

Ã„yritie 4

Vantaa

01510

Finland

Serilization:

Authorised Representative
Name: Philips Electronics UK Ltd
Address:

Ascent 1 Farnborough Aerospace Centre

Farnborough

Hampshire GU14 6XW

England United Kingdom

Code/Term Type

Radiation therapy treatment planning positioning kit Class I

Patient transfer system, manual Class I

MRI system application software 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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Code/Term		Type
Radiation therapy treatment planning positioning kit		Class I
Patient transfer system, manual		Class I
MRI system application software		Class IIa