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 - SIS Medical AG

Address:

Hungerbüelstrasse 12A

Frauenfeld

8500

Switzerland

Authorised Representative/ UK Responsible Person
Name: VASCULAR PERSPECTIVES LIMITED
Address:

35 WESTGATE

HUDDERSFIELD

WEST YORKSHIRE HD1 1PA

England United Kingdom

Code/Term Type

Catheter/overtube balloon inflator single-use Catheter/overtube balloon inflator single-use Class I

Coronary angioplasty balloon catheter basic Coronary angioplasty balloon catheter basic Class III

Thrombectomy suction catheter Thrombectomy suction catheter 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/overtube balloon inflator single-use	Catheter/overtube balloon inflator single-use	Class I
Coronary angioplasty balloon catheter basic	Coronary angioplasty balloon catheter basic	Class III
Thrombectomy suction catheter	Thrombectomy suction catheter	Class III