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Multiple Chlamydia species immunoglobulin G (IgG) antibody IVD, kit, fluorescent immunoassay - UK MHRA Medical Device Registration

Multiple Chlamydia species immunoglobulin G (IgG) antibody IVD, kit, fluorescent immunoassay is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 114504. 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.

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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In Vitro Diagnostic Device
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Multiple Chlamydia species immunoglobulin G (IgG) antibody IVD, kit, fluorescent immunoassay
MHRA Device ID: 114504โ€ขRef: 114504

Device Type

In Vitro Diagnostic Device

Devices

Multiple Chlamydia species immunoglobulin G (IgG) antibody IVD, kit, fluorescent immunoassay

Type

IVD Annex II List B

Date Registered

Nov 26, 2024

Last Updated

Jun 7, 2024

Manufacturer Information

Address

11331 Valley View St.

Cypress, California, United States

Created Date

Nov 23, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

Central Road

Dartford, England, United Kingdom

Postcode: DA1 5LR

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