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 Atheromed Inc

Address:

1530 O’Brien Drive Suite A

Menlo Park

CA 94025

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

Mechanical atherectomy system catheter peripheral Mechanical atherectomy system catheter peripheral Class IIa

Peripheral vascular guidewire manual Peripheral vascular guidewire manual Class IIa

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
Mechanical atherectomy system catheter peripheral	Mechanical atherectomy system catheter peripheral	Class IIa
Peripheral vascular guidewire manual	Peripheral vascular guidewire manual	Class IIa