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 - Hangzhou Lifereal Biotechnology Co. Ltd.

Address:

1st & 2nd Floor of Building 4 and 1st Floor of Building 3 No 21 Futai Road Zhongtai Street Yuhang District

Hangzhou

310000

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

Thermal cycler nucleic acid amplification analyser IVD laboratory Thermal cycler nucleic acid amplification analyser IVD laboratory IVD General

General specimen container IVD additive/medium General specimen container IVD additive/medium 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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Code/Term		Type
Thermal cycler nucleic acid amplification analyser IVD laboratory	Thermal cycler nucleic acid amplification analyser IVD laboratory	IVD General
General specimen container IVD additive/medium	General specimen container IVD additive/medium	IVD General