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 Healthcare (Suzhou) Co. Ltd.

Address:

No. 258 ZhongYuan Road Suzhou Industrial Park

Suzhou

215024

China

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

Stationary basic diagnostic x-ray system digital Stationary basic diagnostic x-ray system digital Class I

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

MRI system coil radio-frequency MRI system coil radio-frequency Class IIb

Full-body CT system Full-body CT system Class IIa

Full-body CT system Full-body CT system 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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Code/Term		Type
Stationary basic diagnostic x-ray system digital	Stationary basic diagnostic x-ray system digital	Class I
Full-body MRI system superconducting magnet	Full-body MRI system superconducting magnet	Class IIb
MRI system coil radio-frequency	MRI system coil radio-frequency	Class IIb
Full-body CT system	Full-body CT system	Class IIa
Full-body CT system	Full-body CT system	Class IIb