October 31, 2017 by CUI Inc
The IEC 60601-1 standard, which provides general requirements that address the basic safety and essential performance of medical electrical equipment, has evolved through a number revisions since its first publication in 1977. Keeping on top of these revisions and new editions of the standard has proven to be a challenge for medical device designers because of their many regional variations and differing adoption timelines around the globe.
With the introduction of collateral standard IEC 60601-1-2 (“Electromagnetic disturbances – Requirements and tests”) in 2014, now commonly referred to as the “4th edition,” the global landscape has become even more unclear. To help illustrate the adoption timeline of IEC 60601-1 as it relates to various territories worldwide, we have developed this country compliance infographic that highlights the evolution of the different editions now and into the future.
For more information on the IEC 60601-1 medical design standards and regional compliance timelines, check out our in-depth application note
View our full line of medical 60601-1 4th edition compliant power supplies
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