Glomerular basement membrane antibody (Goodpasture antibody) IVD, kit, fluorescent immunoassay - UK MHRA Medical Device Registration

Glomerular basement membrane antibody (Goodpasture antibody) IVD, kit, fluorescent immunoassay is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 142807. The device is manufactured by Phadia AB from Sweden, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Thermo Fisher Diagnostics Ltd..

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Glomerular basement membrane antibody (Goodpasture antibody) IVD, kit, fluorescent immunoassay

MHRA Device ID: 142807•Ref: 142807

Device Type

In Vitro Diagnostic Device

Devices

Glomerular basement membrane antibody (Goodpasture antibody) IVD, kit, fluorescent immunoassay

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Oct 3, 2024

Manufacturer Information

Name

Phadia AB

Address

Rapsagatan 7P PO. Box 6460 751 37 Uppsala

Uppsala, Uppsala Län, Sweden

Created Date

Apr 1, 2022

Authorized Representative

Name

Thermo Fisher Diagnostics Ltd.

Relationship Type

UK Responsible Person

Address

Stafford House Boundary Way

Hemel Hempstead, England, United Kingdom

Postcode: HP27GE

DJ Fang

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Glomerular basement membrane antibody (Goodpasture antibody) IVD, kit, fluorescent immunoassay - UK MHRA Medical Device Registration

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