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 Medical Systems Nederland B.V.

Address:

MR Veenpluis 6

Best

5684 PC

Netherlands

Authorised Representative/ UK Responsible Person
Name: Philips Electronics UK Ltd
Address:

Ascent 1 Farnborough Aerospace Centre

Farnborough

Hampshire GU14 6XW

England United Kingdom

Code/Term Type

Full-body MRI system superconducting magnet Full-body MRI system superconducting magnet Class I

MRI system coil radio-frequency MRI system coil radio-frequency Class IIa

MRI system application software MRI system application software Class IIb

Full-body MRI system superconducting magnet Full-body MRI system superconducting magnet Class IIb

Patient transfer system manual Patient transfer system manual Class I

Radiation therapy treatment planning positioning kit Radiation therapy treatment planning positioning kit 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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Code/Term		Type
Full-body MRI system superconducting magnet	Full-body MRI system superconducting magnet	Class I
MRI system coil radio-frequency	MRI system coil radio-frequency	Class IIa
MRI system application software	MRI system application software	Class IIb
Full-body MRI system superconducting magnet	Full-body MRI system superconducting magnet	Class IIb
Patient transfer system manual	Patient transfer system manual	Class I
Radiation therapy treatment planning positioning kit	Radiation therapy treatment planning positioning kit	Class I