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

Serilization:

Authorised Representative
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 Class I

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