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Home » EU Releases Working Document of MDR/IVDR Borderline and Classification Manual
EU Releases Working Document of MDR/IVDR Borderline and Classification Manual
The EU released last week a working draft of a manual to help devicemakers understand where the line between a device and another type of product falls and how devices are classified under the Medical Devices Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR).