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 Fitfaith Technology Co. Ltd.

Address:

501 Building B5 Dongfang Jianfu Yijing Industrial City Tianliao Community Yutang Street Guangming District

Shenzhen

518132

China

Authorised Representative/ UK Responsible Person
Name: MedPath Limited
Address:

27 Old Gloucester Street

London

WC1N 3AX

England United Kingdom

Code/Term Type

Pulse oximeter Pulse oximeter 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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