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 - Draeger Safety AG & Co

Address:

Revalstraße 1

Lübeck

23560

Germany

Authorised Representative/ UK Responsible Person
Name: Draeger Medical UK Ltd
Address:

The Willows Mark Road Hertfordshire HP2 7BW

hemel hempstead

Hertfordshire HP2 7BW

England United Kingdom

Code/Term Type

SARS-CoV-2 antigen IVD kit rapid ICT clinical SARS-CoV-2 antigen IVD kit rapid ICT clinical IVD General

Multiple drugs of abuse IVD kit rapid ICT clinical Multiple drugs of abuse IVD kit rapid ICT clinical IVD Devices for Self-Testing

Multiple drugs of abuse IVD kit rapid ICT clinical Multiple drugs of abuse IVD kit rapid ICT clinical 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
SARS-CoV-2 antigen IVD kit rapid ICT clinical	SARS-CoV-2 antigen IVD kit rapid ICT clinical	IVD General
Multiple drugs of abuse IVD kit rapid ICT clinical	Multiple drugs of abuse IVD kit rapid ICT clinical	IVD Devices for Self-Testing
Multiple drugs of abuse IVD kit rapid ICT clinical	Multiple drugs of abuse IVD kit rapid ICT clinical	IVD General