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 - Huawei Device Co. Ltd.

Address:

No.2 of Xincheng Road Songshan Lake Zone

Dongguan

Guangdong 523808

China

Authorised Representative/ UK Responsible Person
Name: HUAWEI TECHNOLOGIES (UK) CO. LTD.
Address:

300 South Oak Way

Reading

RG2 6AD

England United Kingdom

Code/Term Type

Cardiac electrophysiology application software Cardiac electrophysiology application software Class IIb

Automatic-inflation electronic sphygmomanometer portable arm/wrist Automatic-inflation electronic sphygmomanometer portable arm/wrist 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
Cardiac electrophysiology application software	Cardiac electrophysiology application software	Class IIb
Automatic-inflation electronic sphygmomanometer portable arm/wrist	Automatic-inflation electronic sphygmomanometer portable arm/wrist	Class IIa