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 - Qualpro Diagnostics - A Division of Tulip Diagnostics (P) Ltd.

Address:

Plot No.88/89 Phase IIC Verna Industrial Estate

Verna

Goa 403722

India

Authorised Representative/ UK Responsible Person
Name: CMC Medical Devices LTD
Address:

Office 32 19-21 Crawford Street

London

W1H 1PJ

United Kingdom

Code/Term Type

Multiple Plasmodium species antigen IVD kit enzyme immunoassay (EIA) Multiple Plasmodium species antigen IVD kit enzyme immunoassay (EIA) 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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