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 - Uscom Limited

Address:

Level 8 66 Clarence Street

Sydney

NSW 2000

Australia

Authorised Representative/ UK Responsible Person
Name: Advena Ltd
Address:

Pure Offices Plato Close

Warwick

CV34 6WE

England United Kingdom

Code/Term Type

Automatic-inflation electronic sphygmomanometer non-portable Automatic-inflation electronic sphygmomanometer non-portable Class IIa

Noninvasive haemodynamic monitoring system Noninvasive haemodynamic monitoring system 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
Automatic-inflation electronic sphygmomanometer non-portable	Automatic-inflation electronic sphygmomanometer non-portable	Class IIa
Noninvasive haemodynamic monitoring system	Noninvasive haemodynamic monitoring system	Class IIa