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 - Shenzhen Medoo Medical Tech. Co. Ltd.

Address:

Room 1014-1017 B Block Liyuan Business Building Dongbin Road South Nanshan District

Shenzhen

Guangdong 518054

China

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

27 Old Gloucester Street

London

WC1N 3AX

England United Kingdom

Code/Term Type

Coronary angioplasty balloon catheter basic Coronary angioplasty balloon catheter basic 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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