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 India Limited

Address:

Plot no. B-79 MIDC Phase-II Chakan Taluka - Khed Village - Savardari

Pune

Maharashtra 410501

India

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

Mobile general-purpose fluoroscopic x-ray system analogue Mobile general-purpose fluoroscopic x-ray system analogue 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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