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 - Changsha Renji Medical Equipment Co. Ltd.

Address:

Workshop 201 Stage 4 Changsha E Center No.18 Xiangtai Road Liuyang Jingkai District

Changsha

Hunan 410300

China

Authorised Representative/ UK Responsible Person
Name: KINGSMEAD SERVICE LIMITED
Address:

19 MEZZANINE FLOOR 19-21 CRAWFORD STREET

London

W1H 1PJ

England United Kingdom

Code/Term Type

Oral/upper respiratory tract specimen collection kit IVD clinical Oral/upper respiratory tract specimen collection kit IVD clinical IVD General

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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