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 - Association of Medicine and Analytics Company Limited (AMA Co Ltd)

Address:

17 line of Vasilievsky Island 4-6

Saint-Petersburg

199034

Russia

Authorised Representative/ UK Responsible Person
Name: Creo Medical UK Limited
Address:

Bridgend Road Industrial Estate

Dingwall

Ross-Shire. Scotland IV15 9QF

Scotland United Kingdom

Code/Term Type

Helicobacter pylori urease IVD kit chromogenic Helicobacter pylori urease IVD kit chromogenic 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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