HIV1/HIV2 antigen/antibody IVD, kit, chemiluminescent immunoassay - UK MHRA Medical Device Registration

HIV1/HIV2 antigen/antibody IVD, kit, chemiluminescent immunoassay is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 133373. The device is manufactured by Bio-Rad Laboratories, Inc., Clinical Immunology Division (CID) from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is BIO-RAD LABORATORIES 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.

Free Database

MHRA Registered

In Vitro Diagnostic Device

🇬🇧

HIV1/HIV2 antigen/antibody IVD, kit, chemiluminescent immunoassay

MHRA Device ID: 133373•Ref: 133373

Device Type

In Vitro Diagnostic Device

Devices

HIV1/HIV2 antigen/antibody IVD, kit, chemiluminescent immunoassay

Type

IVD Annex II List A

Date Registered

Nov 26, 2024

Last Updated

Apr 16, 2024

Manufacturer Information

Name

Bio-Rad Laboratories, Inc., Clinical Immunology Division (CID)

Address

5500 East 2nd St.

Benicia, California, United States

Created Date

Dec 29, 2021

Authorized Representative

Name

BIO-RAD LABORATORIES LIMITED

Relationship Type

UK Responsible Person

Address

The Junction 3rd And 4th Floor, Station Road, Watford, United Kingdom, WD17 1ET

WATFORD, Hertfordshire, England, United Kingdom

Postcode: wd17 1et

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Other Products from Bio-Rad Laboratories, Inc., Clinical Immunology Division (CID) (10)

Other Products from Same Authorized Representative (10)

HIV1/HIV2 antigen/antibody IVD, kit, chemiluminescent immunoassay - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

Epstein-Barr virus (EBV) heterophile antibody IVD, kit, rapid ICT, clinical

Influenza A/B virus antigen IVD, kit, rapid ICT, clinical

Streptococcus pneumoniae antigen IVD, kit, rapid ICT, clinical

Dengue virus antigen/antibody IVD, kit, rapid ICT, clinical

Helicobacter pylori antigen IVD, kit, rapid ICT, clinical

Legionella pneumophila antigen IVD, kit, rapid ICT, clinical

Respiratory syncytial virus (RSV) antigen IVD, kit, rapid ICT, clinical

SARS-CoV-2 antigen IVD, kit, rapid ICT, self-testing

Trichomonas vaginalis antigen IVD, kit, rapid ICT, clinical

Multiple gastrointestinal virus antigen IVD, kit, rapid ICT, clinical

Multiplex analyser IVD, laboratory

Multiple antinuclear antibody (ANA) screening IVD, control

Cyclic citrullinated peptide antibody (anti-CCP) IVD, control

Multiple Coeliac disease-associated antibody IVD, calibrator

Multiple vasculitis-associated antibody IVD, kit, multiplex

Cyclic citrullinated peptide antibody (anti-CCP) IVD, calibrator

Multiple antinuclear antibody (ANA) screening IVD, reagent

Cyclic citrullinated peptide antibody (anti-CCP) IVD, kit, multiplex

Microscope slide coverslip IVD

HIV1/HIV2 antigen/antibody IVD, calibrator

Antibody identification panel reagent red blood cell IVD, kit, agglutination

ABO/Rh multiple blood grouping IVD, kit, agglutination

Anti-E [RH005] red blood cell grouping IVD, antibody

Anti-Jk^a red blood cell grouping IVD, antibody

Anti-Le^a red blood cell grouping IVD, antibody

Anti-Le^b red blood cell grouping IVD, antibody

Anti-N red blood cell grouping IVD, antibody

Anti-Rh(D) red blood cell grouping IVD, antibody

Anti-S [MNS004] red blood cell grouping IVD, antibody

Antisera matrix (non-reactive) IVD, control