Nucleosomal antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

Nucleosomal antibody IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 125543. The device is manufactured by INOVA Diagnostics from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Werfen Ltd.

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Nucleosomal antibody IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 125543•Ref: 125543

Device Type

In Vitro Diagnostic Device

Devices

Nucleosomal antibody IVD, kit, enzyme immunoassay (EIA)

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Nov 22, 2024

Manufacturer Information

Name

INOVA Diagnostics

Address

9900 Old Grove Road

San Diego, United States

Created Date

Dec 21, 2021

Authorized Representative

Name

Werfen Ltd

Relationship Type

UK Responsible Person

Address

712 The Quadrant, Cavendish Avenue, Birchwood, Warrington WA3 6DE Manchester

Manchester, England, United Kingdom

Postcode: WA3 6DE

DJ Fang

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Other Products from Same Authorized Representative (10)

Nucleosomal antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

Device Type

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Last Updated

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Created Date

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Address

DJ Fang

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