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 - Mercator MedSystems Inc.

Address:

1900 Powell Street Suite 800

Emeryville

California 94608

United States

Authorised Representative/ UK Responsible Person
Name: Emergo Consulting (UK) Limited
Address:

Compass House Vision Park Histon c/o Cr360 – UL International

Cambridge

CB24 9BZ

England United Kingdom

Code/Term Type

Bronchial balloon catheter Bronchial balloon catheter Class IIa

Coronary artery infusion catheter Coronary artery infusion catheter 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
Bronchial balloon catheter	Bronchial balloon catheter	Class IIa
Coronary artery infusion catheter	Coronary artery infusion catheter	Class IIa