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

Histamine 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 92084. The device is manufactured by Immunotech s.r.o from Czechia, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Beckman Coulter UK Ltd.

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Histamine antibody IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 92084•Ref: 92084

Device Type

In Vitro Diagnostic Device

Devices

Histamine antibody IVD, kit, enzyme immunoassay (EIA)

Type

IVD General

Date Registered

Feb 23, 2024

Last Updated

Feb 2, 2024

Manufacturer Information

Name

Immunotech s.r.o

Address

Radiova 1122/1 102 00 Prague 10

Prague, Czechia

Created Date

Aug 3, 2021

Authorized Representative

Name

Beckman Coulter UK Ltd

Relationship Type

UK Responsible Person

Address

Oakley Court Kingsmead Busines sPark London Rd

High Wycombe, Bucks, United Kingdom

Postcode: HP11 1JU

DJ Fang

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

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