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 - Microbix

Address:

Microbix 265 Watline Ave.

Mississauga

Ontario L4Z 1P3

Canada

Authorised Representative/ UK Responsible Person
Name: R-Biopharm Rhone Ltd
Address:

Mazars 30 Old Bailey

London

EC4M 7AU

England United Kingdom

Code/Term Type

Human papillomavirus (HPV) high-risk strain nucleic acid IVD control Human papillomavirus (HPV) high-risk strain nucleic acid IVD control IVD General

SARS-CoV-2 nucleic acid IVD control SARS-CoV-2 nucleic acid IVD control IVD General

Mycoplasma genitalium nucleic acid IVD control Mycoplasma genitalium nucleic acid IVD control IVD General

Multiple-type sexually transmitted pathogen nucleic acid IVD control Multiple-type sexually transmitted pathogen nucleic acid IVD control 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
Human papillomavirus (HPV) high-risk strain nucleic acid IVD control	Human papillomavirus (HPV) high-risk strain nucleic acid IVD control	IVD General
SARS-CoV-2 nucleic acid IVD control	SARS-CoV-2 nucleic acid IVD control	IVD General
Mycoplasma genitalium nucleic acid IVD control	Mycoplasma genitalium nucleic acid IVD control	IVD General
Multiple-type sexually transmitted pathogen nucleic acid IVD control	Multiple-type sexually transmitted pathogen nucleic acid IVD control	IVD General