United Kingdom MHRA device registration 120842

Multiple Rickettsia species (spotted fever group) immunoglobulin G (IgG) antibody IVD, control

United Kingdom·In Vitro Diagnostic Device·DiaSorin Molecular LLC·Registered Nov 26, 2024

Registration details

Device ID: 120842
MHRA Reference Number: 120842
Date Registered: Nov 26, 2024
Last Updated: Jun 7, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Multiple Rickettsia species (spotted fever group) immunoglobulin G (IgG) antibody IVD, control
Type: IVD General

Manufacturer

Name: DiaSorin Molecular LLC
Address: 11331 Valley View St.
Cypress, California, United States
Created Date: Nov 23, 2021

Authorized Representative

Name: DiaSorin Italia S.p.A. UK Branch
Relationship Type: UK Responsible Person
Address: Central Road
Dartford, England, United Kingdom
Postcode: DA1 5LR

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About this record

Multiple Rickettsia species (spotted fever group) immunoglobulin G (IgG) antibody IVD, control is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 120842. The device is manufactured by DiaSorin Molecular LLC from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is DiaSorin Italia S.p.A. UK Branch.

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