Using IEC 60601-1-9 as a Competitive Advantage


Download this white paper to learn how IEC 60601-1-9 can be used to promote sustainability claims for your medical devices including:

Regulatory requirements

Impact on CB Scheme

Benefits of applying this collateral standard

How to demonstrate compliance

Please click here for the details.


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Europe - May 2020

Denmark: New rules mean non-serious adverse events may also need to be reported EU: Application of Regulation (EU) 2017/745 postponed by one year EU: Continued use of lead as a thermal stabiliser in P

EU: MDR delayed to 26 May 2021

Application of the Medical Devices Regulation (MDR) has been deferred by one year, until 26 May 2021, for fear of shortage or delay in getting essential medical devices needed to combat Covid-19. The

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