Rubella virus immunoglobulin G (IgG) antibody IVD, control - UK MHRA Medical Device Registration

Rubella virus immunoglobulin G (IgG) antibody IVD, control is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 69007. The device is manufactured by Abbott Ireland Diagnostics Division from Ireland, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Abbott Laboratories Limited.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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Rubella virus immunoglobulin G (IgG) antibody IVD, control

MHRA Device ID: 69007•Ref: 69007

Device Type

In Vitro Diagnostic Device

Devices

Rubella virus immunoglobulin G (IgG) antibody IVD, control

Type

IVD Annex II List B

Date Registered

Nov 26, 2024

Last Updated

May 22, 2024

Manufacturer Information

Name

Abbott Ireland Diagnostics Division

Address

Finisklin Business Park

Sligo, Ireland

Created Date

Mar 9, 2021

Authorized Representative

Name

Abbott Laboratories Limited

Relationship Type

UK Responsible Person

Address

Abbott House, Vanwall Business Park, Vanwall Road

Maidenhead, Berkshire, England, United Kingdom

Postcode: SL64XE

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Rubella virus immunoglobulin G (IgG) antibody IVD, control - UK MHRA Medical Device Registration

Device Type

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Address

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