United Kingdom MHRA device registration 148663

SARS-CoV-2 immunoglobulin G (IgG) antibody IVD, control

United Kingdom·In Vitro Diagnostic Device·Cliniqa Corporation·Registered Nov 26, 2024

Registration details

Device ID: 148663
MHRA Reference Number: 148663
Date Registered: Nov 26, 2024
Last Updated: Nov 19, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: SARS-CoV-2 immunoglobulin G (IgG) antibody IVD, control
Type: IVD General

Manufacturer

Name: Cliniqa Corporation
Address: 495 Enterprise Street
San Marcos, California, United States
Created Date: May 27, 2022

Authorized Representative

Name: UKCApartner4U Limited
Relationship Type: UK Responsible Person
Address: 7 CAMPION WAY
BINGHAM, NOTTINGHAM, England, United Kingdom
Postcode: NG13 8 TR

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About this record

SARS-CoV-2 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 148663. The device is manufactured by Cliniqa Corporation from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is UKCApartner4U Limited.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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