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 - Hexacath

Address:

4 passage Saint-Antoine

RUEIL-MALMAISON

Nanterre

Hauts-De-Seine 92500

France

Authorised Representative/ UK Responsible Person
Name: Hexacath Limited
Address:

Suite 31 80 Churchill Square

Kings Hill

Kent ME19 4YU

England United Kingdom

Code/Term Type

Bare-metal coronary artery stent Bare-metal coronary artery stent Class III

Coronary artery infusion catheter Coronary artery infusion catheter Class IIb

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
Bare-metal coronary artery stent	Bare-metal coronary artery stent	Class III
Coronary artery infusion catheter	Coronary artery infusion catheter	Class IIb