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 152325. The device is manufactured by Accelerate Diagnostics, Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qarad UK Ltd..

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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In Vitro Diagnostic Device

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Buffered sample diluent IVD

MHRA Device ID: 152325•Ref: 152325

Device Type

In Vitro Diagnostic Device

Devices

Buffered sample diluent IVD

Type

Class A

Date Registered

Nov 26, 2024

Last Updated

May 9, 2024

Manufacturer Information

Name

Accelerate Diagnostics, Inc.

Address

3950 S. Country Club Road #470

Tucson, United States

Created Date

Jun 23, 2022

Authorized Representative

Name

Qarad UK Ltd.

Relationship Type

UK Responsible Person

Address

8 Northumberland Ave

Westminster, London , England, United Kingdom

Postcode: WC2N 5BY

DJ Fang

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Buffered sample diluent IVD

Type: In Vitro Diagnostic Device

Registered: Nov 26, 2024

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Buffered sample diluent IVD - UK MHRA Medical Device Registration

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