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 - Volcano Corporation- San Diego

Address:

3721 Valley Centre Dr Ste 500

San Diego

CA 92130

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

Catheter-tip transducer pressure Catheter-tip transducer pressure Class III

Intravascular ultrasound imaging catheter single-use Intravascular ultrasound imaging catheter single-use Class IIa

Catheter-tip transducer pressure Catheter-tip transducer pressure Class III

Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Class IIa

Intravascular ultrasound imaging catheter single-use Intravascular ultrasound imaging catheter single-use Conformity Assessment Certificate Expired 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
Catheter-tip transducer pressure	Catheter-tip transducer pressure	Class III
Intravascular ultrasound imaging catheter single-use	Intravascular ultrasound imaging catheter single-use	Class IIa
Catheter-tip transducer pressure	Catheter-tip transducer pressure	Class III
Cardiovascular ultrasound imaging system	Cardiovascular ultrasound imaging system	Class IIa
Intravascular ultrasound imaging catheter single-use	Intravascular ultrasound imaging catheter single-use Conformity Assessment Certificate Expired	Class III