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

Tissue transglutaminase 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 81577. The device is manufactured by Eurospital S.p.A. from Italy, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qarad UK Ltd..

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Tissue transglutaminase antibody IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 81577•Ref: 81577

Device Type

In Vitro Diagnostic Device

Devices

Tissue transglutaminase antibody IVD, kit, enzyme immunoassay (EIA)

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Oct 23, 2024

Manufacturer Information

Name

Eurospital S.p.A.

Address

Via Flavia 122

TRIESTE, Friuli-Venezia Giulia, Italy

Created Date

May 20, 2021

Authorized Representative

Name

Qarad UK Ltd.

Relationship Type

UK Responsible Person

Address

8 Northumberland Ave

Westminster, London , England, United Kingdom

Postcode: WC2N 5BY

DJ Fang

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

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