Eurofins Electric & Electronics Finland Oy designated as IVDR Notified Body
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We are delighted to announce that Eurofins Electric & Electronics Finland Oy has been officially designated as a Notified Body to the In Vitro Diagnostics Medical Device Regulation (EU 2017/746) by Finnish Competent Authority Fimea.
This prestigious designation marks a significant milestone in our commitment to upholding the highest standards of quality and safety in the fields of in vitro diagnostic medical devices and medical devices. With this recognition, Eurofins Electric & Electronics Finland Oy becomes one of the select conformity assessment bodies designated for both IVDR and MDR in Europe.
We invite you to visit the NANDO website for comprehensive details on our scope.
At Eurofins Electric & Electronics Finland Oy, we take great pride in our dedication to regulatory compliance and our role in ensuring that in vitro diagnostic medical devices and medical devices meet the stringent requirements of IVDR and MDR. We are committed to providing exceptional service and expertise to our clients.
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