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How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
How to conform with the legal requirements for placing medical devices on the market.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
UKHSA are providing an update to previous advice regarding contaminated non-sterile alcohol-free wipes in response to continuing detection of cases and a recent death attributable to Burkholderia stabilis infection.
Information about medical devices that the public can buy for personal use and how we make sure they are safe and effective.
This document outlines guidance for cleaning and decontamination of non-healthcare settings.
If your organisation supports people in Copeland, Allerdale or Warrington you may be eligible to apply for a grant/reusable equipment.
What you need to do before your product can be placed on the Great Britain market with a UKCA mark.
Information about how the MHRA regulates medical devices in Northern Ireland and what legislation applies to manufacturers and suppliers.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
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