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 - Analyticon Biotechnologies GmbH

Address:

Am Muehlenberg 10

Lichtenfels

35104

Germany

Authorised Representative/ UK Responsible Person
Name: Sterilab Services Ltd.
Address:

Unit 700 Street 5

Thorp Arch Estate

Wetherby

West Yorkshire LS23 7FZ

England United Kingdom

Code/Term Type

Multiple urine analyte IVD control Multiple urine analyte IVD control IVD General

Multiple urine analyte IVD kit rapid colorimetric clinical Multiple urine analyte IVD kit rapid colorimetric clinical IVD General

Urine analyser IVD point-of-care Urine analyser IVD point-of-care 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 urine analyte IVD control	Multiple urine analyte IVD control	IVD General
Multiple urine analyte IVD kit rapid colorimetric clinical	Multiple urine analyte IVD kit rapid colorimetric clinical	IVD General
Urine analyser IVD point-of-care	Urine analyser IVD point-of-care	IVD General