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 Prunus Medical Co. Ltd.

Address:

6th Floor and Zone A of 9th Floor Block C No. 71-3 Xintian Road Fuyong Street Bao'an District 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

Anaesthesia workstation general-purpose Anaesthesia workstation general-purpose Class IIb

General-purpose intensive-care ventilator General-purpose intensive-care ventilator Class IIb

Neonatal/adult intensive-care ventilator Neonatal/adult intensive-care ventilator Class IIb

Transport electric ventilator Transport electric ventilator Class IIb

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
Anaesthesia workstation general-purpose	Anaesthesia workstation general-purpose	Class IIb
General-purpose intensive-care ventilator	General-purpose intensive-care ventilator	Class IIb
Neonatal/adult intensive-care ventilator	Neonatal/adult intensive-care ventilator	Class IIb
Transport electric ventilator	Transport electric ventilator	Class IIb