IEC/EN 60601-1-2 EMC for Medical Devices

Medical Device Testing

To find out more about the new 4th Edition changes to IEC/EN 60601-1-2, please contact us or request a quote in the sidebar to the right.

D.L.S provides testing services for electromagnetic compatibility to IEC/EN 60601-1-2 including the recently published updates for the 4th edition, used to show compliance to the Medical Device Directive 93/42/EEC.

Individual testing standards for compliances include the following:

Included with updated EMC testing procedures and test levels are formal requirements for manufacturers to not only include risk assessment, but detail testing parameters to be used for the compliance process, which would insure that the areas identified in the risk assessment are clearly defined and addressed. This process is required as part of meeting the essential performance requirements for the EU Medical Device Directive, United States FDA submission, and other global compliance requirements.

Updated collateral Medical Device standards include new EMC requirements:

D.L.S. offers a streamlined program for medical device approval includes the following aspects:

We can ensure your product meets all requirements of the Medical Device Directive, effectively allowing your product to bear the CE Mark in the EU and meet the FDA requirements in the US, and access other global markets.

D.L.S. offers:

Medical Device compliance regulations include includes basic safety and essential performance testing found under IEC 60601-1. D.L.S. can include this testing as well, plus any related collateral or accessory standards in your compliance program. More information on our medical Product Safety capabilities here.

For more information, please contact Jack Black at 847-537-6400 or request a quote online through the sidebar on the right.



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