Multiple Plasmodium species antigen IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

Multiple Plasmodium species antigen IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 146466. The device is manufactured by Qualpro Diagnostics - A Division of Tulip Diagnostics (P) Ltd. from India, classified as In Vitro Diagnostic Device. The authorized representative in the UK is CMC Medical Devices LTD.

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

MHRA Device ID: 146466•Ref: 146466

Device Type

In Vitro Diagnostic Device

Devices

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

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Oct 4, 2023

Manufacturer Information

Name

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

Address

Plot No.88/89, Phase IIC, Verna Industrial Estate

Verna, Goa, India

Created Date

May 4, 2022

Authorized Representative

Name

CMC Medical Devices LTD

Relationship Type

UK Responsible Person

Address

Office 32 19-21 Crawford Street

London, United Kingdom

Postcode: W1H 1PJ

DJ Fang

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Multiple Plasmodium species antigen IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

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