United Kingdom MHRA device registration 194929

C-reactive protein (CRP) IVD, kit, rapid ICT, clinical

United Kingdom·In Vitro Diagnostic Device·PRIMA Lab SA·Registered Nov 26, 2024

Registration details

Device ID: 194929
MHRA Reference Number: 194929
Date Registered: Nov 26, 2024
Last Updated: May 22, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: C-reactive protein (CRP) IVD, kit, rapid ICT, clinical
Type: IVD General

Manufacturer

Name: PRIMA Lab SA
Address: Via Antonio Monti Balerna
Balerna, Mendrisio, Switzerland
Created Date: Jul 9, 2021

Authorized Representative

Name: Qarad UK Ltd.
Relationship Type: UK Responsible Person
Address: 8 Northumberland Ave
Westminster, London , England, United Kingdom
Postcode: WC2N 5BY

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About this record

C-reactive protein (CRP) IVD, kit, rapid ICT, clinical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 194929. The device is manufactured by PRIMA Lab SA from Switzerland, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qarad UK Ltd..

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