Buffered sample diluent IVD - UK MHRA Medical Device Registration

Buffered sample diluent IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 184017. 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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Buffered sample diluent IVD

MHRA Device ID: 184017•Ref: 184017

Device Type

In Vitro Diagnostic Device

Devices

Buffered sample diluent IVD

Type

IVD General

Date Registered

Feb 23, 2024

Last Updated

Jan 13, 2024

Manufacturer Information

Name

Abbott Ireland Diagnostics Division

Address

Lisnamuck, Longford, Co. Longford

Longford, Ireland

Created Date

Sep 15, 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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Buffered sample diluent IVD - UK MHRA Medical Device Registration

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