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 Image Guided Therapy Corporation

Address:

9965 Federal Drive

Colorado Springs

CO 80921

United States

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

Vascular guide-catheter single-use Vascular guide-catheter single-use Class IIa

Coronary angioplasty balloon catheter cutting/scoring Coronary angioplasty balloon catheter cutting/scoring Class III

Peripheral angioplasty balloon catheter drug-coated Peripheral angioplasty balloon catheter drug-coated Class III

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
Vascular guide-catheter single-use	Vascular guide-catheter single-use	Class IIa
Coronary angioplasty balloon catheter cutting/scoring	Coronary angioplasty balloon catheter cutting/scoring	Class III
Peripheral angioplasty balloon catheter drug-coated	Peripheral angioplasty balloon catheter drug-coated	Class III