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 - miDiagnostics nv

Address:

Gaston Geenslaan 1

Leuven

Leuven

Vlaams-Brabant 3001

Belgium

Authorised Representative/ UK Responsible Person
Name: IVDeology UKRP Ltd
Address:

22-23 The Joiners Shop Historic Dockyard

Chatham

Rochester

Kent ME4 4TZ

England United Kingdom

Code/Term Type

Oral/respiratory tract specimen container IVD additive/medium Oral/respiratory tract specimen container IVD additive/medium Class A

Thermal cycler nucleic acid amplification analyser IVD laboratory Thermal cycler nucleic acid amplification analyser IVD laboratory Class A

SARS-CoV-2 nucleic acid IVD reagent SARS-CoV-2 nucleic acid IVD reagent 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
Oral/respiratory tract specimen container IVD additive/medium	Oral/respiratory tract specimen container IVD additive/medium	Class A
Thermal cycler nucleic acid amplification analyser IVD laboratory	Thermal cycler nucleic acid amplification analyser IVD laboratory	Class A
SARS-CoV-2 nucleic acid IVD reagent	SARS-CoV-2 nucleic acid IVD reagent	IVD General