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 - Guangdong Kindly Medical Device Group Co. Ltd.

Address:

Room 101 Building A No.288 East Airport Road Jinwan District

Zhuhai

Guangdong 519040

China

Authorised Representative/ UK Responsible Person
Name: Prosum Medical Limited
Address:

Unit 14 Cowley Mill Road Trade City Business Park

Uxbridge

UB8 2DB

England United Kingdom

Code/Term Type

General-purpose syringe single-use General-purpose syringe single-use Class IIa

General-purpose syringe/needle General-purpose syringe/needle Class IIa

Electronic gravity infusion controller administration set Electronic gravity infusion controller administration set 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
General-purpose syringe single-use	General-purpose syringe single-use	Class IIa
General-purpose syringe/needle	General-purpose syringe/needle	Class IIa
Electronic gravity infusion controller administration set	Electronic gravity infusion controller administration set	Class IIa