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DiaSorin Molecular LLC - Medical Device Manufacturer in United Kingdom

DiaSorin Molecular LLC from United States is a medical device manufacturer with 20 registered products in the UK MHRA database through Pure Global AI's free platform. The company produces 19 unique generic names across 1 device type.

This page provides comprehensive manufacturer intelligence including complete product portfolio and device type distribution. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify manufacturers, analyze portfolios, and discover partnership opportunities efficiently.

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20 Products
1 Types
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DiaSorin Molecular LLC
United States

11331 Valley View St.

Cypress, United States

20
Total Products
19
Generic Names
1
Device Types
19
Generic Names
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Recent Registrations (20 most recent)
Most recently registered products with MHRA

Candida auris nucleic acid IVD, kit, nucleic acid technique (NAT)

Type:

In Vitro Diagnostic Device

Device ID:

213648

Registration Date:

Mar 19, 2025

Candida auris nucleic acid IVD, kit, nucleic acid technique (NAT)

Type:

In Vitro Diagnostic Device

Device ID:

213647

Registration Date:

Mar 19, 2025

Anaplasma phagocytophilum immunoglobulin G (IgG) antibody IVD, kit, fluorescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

120858

Registration Date:

Nov 26, 2024

Bartonella bacilliformis immunoglobulin G (IgG) antibody IVD, reagent

Type:

In Vitro Diagnostic Device

Device ID:

120852

Registration Date:

Nov 26, 2024

Bartonella bacilliformis immunoglobulin M (IgM) antibody IVD, kit, fluorescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

120851

Registration Date:

Nov 26, 2024

Beta-haemolytic Group B Streptococcus nucleic acid IVD, control

Type:

In Vitro Diagnostic Device

Device ID:

120756

Registration Date:

Nov 26, 2024

Clostridium difficile nucleic acid IVD, kit, nucleic acid technique (NAT)

Type:

In Vitro Diagnostic Device

Device ID:

120745

Registration Date:

Nov 26, 2024

Multiple Chlamydia species immunoglobulin M (IgM) antibody IVD, kit, fluorescent immunoassay

Type:

In Vitro Diagnostic Device

Device ID:

114505

Registration Date:

Nov 26, 2024

Coxiella burnetii immunoglobulin G (IgG) antibody IVD, reagent

Type:

In Vitro Diagnostic Device

Device ID:

120846

Registration Date:

Nov 26, 2024

Cytomegalovirus (CMV) nucleic acid IVD, kit, nucleic acid technique (NAT)

Type:

In Vitro Diagnostic Device

Device ID:

114502

Registration Date:

Nov 26, 2024

Dengue virus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)

Type:

In Vitro Diagnostic Device

Device ID:

120768

Registration Date:

Nov 26, 2024

Dengue virus immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)

Type:

In Vitro Diagnostic Device

Device ID:

120769

Registration Date:

Nov 26, 2024

Dengue virus nucleic acid IVD, kit, nucleic acid technique (NAT)

Type:

In Vitro Diagnostic Device

Device ID:

196524

Registration Date:

Nov 26, 2024

Herpes simplex virus 1 & 2 (HSV1 & 2) immunoglobulin G (IgG) antibody IVD, kit, immunoblot

Type:

In Vitro Diagnostic Device

Device ID:

120773

Registration Date:

Nov 26, 2024

JC virus (JCV) antigen IVD, kit, enzyme immunoassay (EIA)

Type:

In Vitro Diagnostic Device

Device ID:

120757

Registration Date:

Nov 26, 2024

Chlamydia trachomatis immunoglobulin A (IgA) antibody IVD, reagent

Type:

In Vitro Diagnostic Device

Device ID:

120849

Registration Date:

Nov 26, 2024

Multiple Human herpesvirus nucleic acid IVD, kit, nucleic acid technique (NAT)

Type:

In Vitro Diagnostic Device

Device ID:

120758

Registration Date:

Nov 26, 2024

Multiple respiratory virus nucleic acid IVD, kit, nucleic acid technique (NAT)

Type:

In Vitro Diagnostic Device

Device ID:

120759

Registration Date:

Nov 26, 2024

Multiple-genus respiratory virus nucleic acid IVD, control

Type:

In Vitro Diagnostic Device

Device ID:

125307

Registration Date:

Nov 26, 2024

Assay adhesive sealing/fixation film IVD

Type:

In Vitro Diagnostic Device

Device ID:

196522

Registration Date:

Nov 26, 2024