Beta-haemolytic Group A Streptococcus streptolysin O antibody IVD, kit, nephelometry/turbidimetry - UK MHRA Medical Device Registration

Beta-haemolytic Group A Streptococcus streptolysin O antibody IVD, kit, nephelometry/turbidimetry is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 172705. The device is manufactured by Beckman Coulter Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Beckman Coulter UK Ltd.

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

🇬🇧

Beta-haemolytic Group A Streptococcus streptolysin O antibody IVD, kit, nephelometry/turbidimetry

MHRA Device ID: 172705•Ref: 172705

Device Type

In Vitro Diagnostic Device

Devices

Beta-haemolytic Group A Streptococcus streptolysin O antibody IVD, kit, nephelometry/turbidimetry

Type

Class B

Date Registered

Nov 26, 2024

Last Updated

Aug 29, 2024

Manufacturer Information

Name

Beckman Coulter Inc.

Address

250 South Kraemer Boulevard

Brea, California, United States

Created Date

Apr 29, 2021

Authorized Representative

Name

Beckman Coulter UK Ltd

Relationship Type

UK Responsible Person

Address

Oakley Court Kingsmead Busines sPark London Rd

High Wycombe, Bucks, United Kingdom

Postcode: HP11 1JU

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Other Products from Beckman Coulter Inc. (10)

Other Products from Same Authorized Representative (10)

Beta-haemolytic Group A Streptococcus streptolysin O antibody IVD, kit, nephelometry/turbidimetry - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

Multiple Salmonella species immunoglobulin G (IgG)/IgM antibody IVD, kit, rapid ICT, clinical

Interleukin-6 (IL-6) IVD, kit, rapid ICT, clinical

Streptococcus pneumoniae antigen IVD, kit, rapid ICT, clinical

Carcinoembryonic antigen (CEA) IVD, kit, fluorescent immunoassay

Clostridium difficile antigen IVD, kit, rapid ICT, clinical

Influenza A/B virus 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

Prothrombin time (PT) IVD, reagent

Hepatitis B virus surface total antibody IVD, kit, chemiluminescent immunoassay

Hepatitis B virus surface total antibody IVD, calibrator

Hepatitis B virus surface total antibody IVD, control

Creatinine IVD, kit, spectrophotometry

Complement components C4/C4c IVD, kit, nephelometry/turbidimetry

Complement factor B IVD, reagent

Chromogen indicator IVD, kit, spectrophotometry

Cannabinoid/cannabinoid metabolite IVD, calibrator

Ceruloplasmin IVD, kit, nephelometry/turbidimetry

Lipoprotein A IVD, calibrator

B-type natriuretic protein/N-terminal pro b-type natriuretic peptide IVD, kit, fluorescent immunoassay

CD105 endoglin marker IVD, antibody

CD11c cell marker IVD, antibody

CD127 cell marker IVD, antibody

CD13 cell marker IVD, antibody

CD138 cell marker IVD, antibody

CD2 T-cell marker IVD, antibody

CD20 cell marker IVD, antibody

CD200 cell marker IVD, antibody

Anti-Mullerian hormone (AMH) IVD, kit, enzyme immunoassay (EIA)