Product Testing and Certification
IEC 61326-2-6: In vitro diagnostic (IVD) medical equipment – EMC requirements
We would like to inform you of the new edition of the standard that covers EMC testing of in-vitro (IVD) medical equipment – IEC 61326-2-6:2020. Newer versions of standards usually introduce minor changes to the already established and accepted te...
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The safety of medical devices
At SIQ, we started testing the safety of medical devices 25 years ago, mainly led by the desire to help Slovenian manufacturers place their innovative medical products on the Slovenian and international market. In 2005, a new c...
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IEC/EN 61010-1 + A1 – Measurement, Control, and Laboratory use
Mid of next year, amendment A1 to EN 61010-1 will become mandatory. Though issued some time ago and already widely used at SIQ, we would like to notify our partners that this amendment will be mandatory in the EU as of 30th May 20...
Find out moreFrom component testing to final products
At SIQ, we are very proud of our wide scope of testing services, with more than 500 standards in our accreditation scope, and of being a member of many international schemes. That enables us to work with manufacturers from many...
Find out moreIEC 61326-2-6: In vitro diagnostic (IVD) medical equipment – EMC requirements
The new edition of the standard that covers EMC testing of in-vitro (IVD) medical equipment – IEC 61326-2-6:2020 has been published recently. The latest version of IEC 61326-2-6 completely rewrites the EMC approach to IVD devices ...
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