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 - Guangzhou Red Pine Medical Instrument Co. Ltd.

Address:

Room 303 308 No. 12 Luoxuan 3 Road Guangzhou International Bioisland Guangzhou

Guangdong Province

510200

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

Endoscopic video image display unit Endoscopic video image display unit Class I

Rigid cystoscope Rigid cystoscope Class IIa

Flexible video ureterorenoscope single-use Flexible video ureterorenoscope single-use 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
Endoscopic video image display unit	Endoscopic video image display unit	Class I
Rigid cystoscope	Rigid cystoscope	Class IIa
Flexible video ureterorenoscope single-use	Flexible video ureterorenoscope single-use	Class IIa