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 - Inpeco SA

Address:

via Torraccia 26

Novazzano

6883

Switzerland

Authorised Representative/ UK Responsible Person
Name: Qarad UK Ltd.
Address:

8 Northumberland Ave

Westminster

London WC2N 5BY

England United Kingdom

Code/Term Type

Specimen processing instrument IVD Specimen processing instrument IVD IVD General

Specimen information management system IVD Specimen information management system IVD 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
Specimen processing instrument IVD	Specimen processing instrument IVD	IVD General
Specimen information management system IVD	Specimen information management system IVD	IVD General