Public Access Database for Medical Device Registration

Registration does not represent any form of accreditation, certification or approval by the UK Competent Authority(MHRA)
Where a conformity assessment certificate is listed as expired, existing products already placed on the market prior to the expiry may not be affected by this expiry and can continue to be used. This expiry stops new products being placed on the market until there is a new certificate of conformity

Manufacturer's By Name

By Device

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Manufacturer's Devices - Accelerate Diagnostics Inc.

Address:

3950 S. Country Club Road #470

Tucson

85714

United States

Authorised Representative/ UK Responsible Person
Name: Qarad UK Ltd.
Address:

8 Northumberland Ave

Westminster

London WC2N 5BY

England United Kingdom

Code/Term Type

Multiple-type bloodstream pathogen nucleic acid IVD kit nucleic acid amplification/mass spectrometry Multiple-type bloodstream pathogen nucleic acid IVD kit nucleic acid amplification/mass spectrometry IVD General

Buffered sample diluent IVD automated/semi-automated system Buffered sample diluent IVD automated/semi-automated system Class A

Buffered sample diluent IVD automated/semi-automated system Buffered sample diluent IVD automated/semi-automated system Class A

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

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Code/Term		Type
Multiple-type bloodstream pathogen nucleic acid IVD kit nucleic acid amplification/mass spectrometry	Multiple-type bloodstream pathogen nucleic acid IVD kit nucleic acid amplification/mass spectrometry	IVD General
Buffered sample diluent IVD automated/semi-automated system	Buffered sample diluent IVD automated/semi-automated system	Class A
Buffered sample diluent IVD automated/semi-automated system	Buffered sample diluent IVD automated/semi-automated system	Class A