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 Yamind Medical Technology Co. Ltd.

Address:

Room A 601 6th Floor G3 Building TCL International E City Xili Street Nanshan District Shenzhen

Guangdong Province

212300

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

Home CPAP unit Home CPAP unit Class IIa

Home BPAP unit Home BPAP unit 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
Home CPAP unit	Home CPAP unit	Class IIa
Home BPAP unit	Home BPAP unit	Class IIa