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

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Manufacturer's Devices - Fast Track Diagnostics Luxembourg SARL

Address:

29 rue Henri Koch Esch-sur-Alzette

Luxembourg

4354

Luxembourg

Authorised Representative/ UK Responsible Person
Name: Siemens Healthcare Diagnostics Limited
Address:

Park View Watchmoor Park

Surrey

Camberley GU15 3YL

England United Kingdom

Code/Term Type

Multiple-type meningitis pathogen nucleic acid IVD kit nucleic acid technique (NAT) Multiple-type meningitis pathogen nucleic acid IVD kit nucleic acid technique (NAT) IVD General

Multiple-type respiratory pathogen nucleic acid IVD kit nucleic acid technique (NAT) Multiple-type respiratory pathogen nucleic acid IVD kit nucleic acid technique (NAT) IVD General

SARS-CoV-2 nucleic acid IVD kit nucleic acid technique (NAT) SARS-CoV-2 nucleic acid IVD kit nucleic acid technique (NAT) IVD General

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 meningitis pathogen nucleic acid IVD kit nucleic acid technique (NAT)	Multiple-type meningitis pathogen nucleic acid IVD kit nucleic acid technique (NAT)	IVD General
Multiple-type respiratory pathogen nucleic acid IVD kit nucleic acid technique (NAT)	Multiple-type respiratory pathogen nucleic acid IVD kit nucleic acid technique (NAT)	IVD General
SARS-CoV-2 nucleic acid IVD kit nucleic acid technique (NAT)	SARS-CoV-2 nucleic acid IVD kit nucleic acid technique (NAT)	IVD General