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

Guangdong

Shenzhen 518101

China

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

2 The Drift

Thurston

Suffolk IP31 3RT

United Kingdom

Code/Term Type

Patient monitoring system module multifunction Patient monitoring system module multifunction Class IIa

Pulse oximeter line-powered Pulse oximeter line-powered Class IIa

Pulse oximeter Pulse oximeter 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
Patient monitoring system module multifunction	Patient monitoring system module multifunction	Class IIa
Pulse oximeter line-powered	Pulse oximeter line-powered	Class IIa
Pulse oximeter	Pulse oximeter	Class IIa