Multiple antinuclear antibody (ANA) screening IVD, kit, fluorescent immunoassay - UK MHRA Medical Device Registration

Multiple antinuclear antibody (ANA) screening IVD, kit, fluorescent immunoassay is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 210835. The device is manufactured by Bio-Rad Laboratories, Inc., Clinical Systems Division (CSD) from United States, classified as In Vitro Diagnostic Device.

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In Vitro Diagnostic Device

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Multiple antinuclear antibody (ANA) screening IVD, kit, fluorescent immunoassay

MHRA Device ID: 210835

Device Type

In Vitro Diagnostic Device

Type

Class B

Status

DREGIY

Date Registered

Feb 14, 2025

Manufacturer Information

Name

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

Address

4000 Alfred Nobel Drive

Hercules, United States

DJ Fang

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Multiple antinuclear antibody (ANA) screening IVD, kit, fluorescent immunoassay - UK MHRA Medical Device Registration

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Date Registered

Name

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