HIV1/HIV2 antigen/antibody IVD, control - UK MHRA Medical Device Registration

HIV1/HIV2 antigen/antibody IVD, control is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 189912. The device is manufactured by Bio-Rad Laboratories, Inc., Clinical Systems Division (CSD) 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.

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In Vitro Diagnostic Device

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HIV1/HIV2 antigen/antibody IVD, control

MHRA Device ID: 189912•Ref: 189912

Device Type

In Vitro Diagnostic Device

Devices

HIV1/HIV2 antigen/antibody IVD, control

Type

Class D

Date Registered

Nov 26, 2024

Last Updated

Apr 16, 2024

Manufacturer Information

Name

Bio-Rad Laboratories, Inc., Clinical Systems Division (CSD)

Address

4000 Alfred Nobel Drive

Hercules, 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

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Other Products from Bio-Rad Laboratories, Inc., Clinical Systems Division (CSD) (10)

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HIV1/HIV2 antigen/antibody IVD, control - UK MHRA Medical Device Registration

Device Type

Devices

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Date Registered

Last Updated

Name

Address

Created Date

Name

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Address

DJ Fang

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