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 Viatom Technology Co. Ltd.

Address:

4E Building 3 Tingwei Industrial Park No.6 Liufang Road Block 67 Xin'an Street

Baoan District

Shenzhen Guangdong

518101

China

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

16 Castle St.

Dover

Kent CT16 1PW

England United Kingdom

Code/Term Type

Manual-inflation electronic sphygmomanometer portable Manual-inflation electronic sphygmomanometer portable Class IIa

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
Manual-inflation electronic sphygmomanometer portable	Manual-inflation electronic sphygmomanometer portable	Class IIa
Automatic-inflation electronic sphygmomanometer portable arm/wrist	Automatic-inflation electronic sphygmomanometer portable arm/wrist	Class IIa