Buffered sample diluent IVD, manual - UK MHRA Medical Device Registration

Buffered sample diluent IVD, manual is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 107708. The device is manufactured by Abbott Laboratories Diagnostics Division from United States, 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, manual

MHRA Device ID: 107708•Ref: 107708

Device Type

In Vitro Diagnostic Device

Devices

Buffered sample diluent IVD, manual

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Aug 10, 2024

Manufacturer Information

Name

Abbott Laboratories Diagnostics Division

Address

Lake County Site 100 Abbott Park Road Abbott Park,

Illinois , Illinois , United States

Created Date

Oct 11, 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, manual - UK MHRA Medical Device Registration

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