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 Jumper Medical Equipment Co. Ltd.

Address:

D Building No. 71 Xintian Road Fuyong Street Bao'an Shenzhen

Guangdong Province

518103

China

Authorised Representative/ UK Responsible Person
Name: SUNGO Certification Company Limited
Address:

3rd Floor 70 Gracechurch Street

London

EC3V 0HR

England United Kingdom

Code/Term Type

Foetal acoustic stimulator Foetal acoustic stimulator Class IIa

Foetal cardiac monitor Foetal cardiac monitor Class IIa

Patient monitoring system module multifunction Patient monitoring system module multifunction Class IIb

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

Pulse oximeter Pulse oximeter Class IIa

Infrared patient thermometer ear/skin Infrared patient thermometer ear/skin 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
Foetal acoustic stimulator	Foetal acoustic stimulator	Class IIa
Foetal cardiac monitor	Foetal cardiac monitor	Class IIa
Patient monitoring system module multifunction	Patient monitoring system module multifunction	Class IIb
Automatic-inflation electronic sphygmomanometer portable arm/wrist	Automatic-inflation electronic sphygmomanometer portable arm/wrist	Class IIa
Pulse oximeter	Pulse oximeter	Class IIa
Infrared patient thermometer ear/skin	Infrared patient thermometer ear/skin	Class IIa