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 - Solaris Medical Technology Inc.

Address:

Zhongjian Industrial Building One #401 18 Yanshan Road

Shekou Nanshan District

Shenzhen

Guangdong 518067

China

Authorised Representative/ UK Responsible Person
Name: Advena Ltd
Address:

Pure Offices Plato Close

Warwick

CV34 6WE

England United Kingdom

Code/Term Type

Pulse oximeter probe reusable Pulse oximeter probe reusable Class IIb

Pulse oximeter probe single-use Pulse oximeter probe single-use Class IIb

Blood pressure cuff reusable Blood pressure cuff reusable Class I

Blood pressure cuff single-use Blood pressure cuff single-use Class I

Electrical-only medical device connection cable reusable Electrical-only medical device connection cable reusable Class I

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
Pulse oximeter probe reusable	Pulse oximeter probe reusable	Class IIb
Pulse oximeter probe single-use	Pulse oximeter probe single-use	Class IIb
Blood pressure cuff reusable	Blood pressure cuff reusable	Class I
Blood pressure cuff single-use	Blood pressure cuff single-use	Class I
Electrical-only medical device connection cable reusable	Electrical-only medical device connection cable reusable	Class I