Foeto-maternal haemorrhage/Kleihauer test IVD, reagent - UK MHRA Medical Device Registration

Foeto-maternal haemorrhage/Kleihauer test IVD, reagent is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 109834. The device is manufactured by Sigma-Aldrich Inc from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Millipore (UK) Ltd.

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Foeto-maternal haemorrhage/Kleihauer test IVD, reagent

MHRA Device ID: 109834•Ref: 109834

Device Type

In Vitro Diagnostic Device

Devices

Foeto-maternal haemorrhage/Kleihauer test IVD, reagent

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Aug 10, 2024

Manufacturer Information

Name

Sigma-Aldrich Inc

Address

3050 Spruce Street

St Louis, United States

Created Date

Oct 26, 2021

Authorized Representative

Name

Millipore (UK) Ltd

Relationship Type

UK Responsible Person

Address

2 Fleming Road Kirkton Campus

Livingston, West Lothian, Scotland, United Kingdom

Postcode: EH54 7BN

DJ Fang

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Foeto-maternal haemorrhage/Kleihauer test IVD, reagent - UK MHRA Medical Device Registration

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