As of 2024, * of all in vitro diagnostics in Europe were classified in class B, meaning they had medium risk for individual patients. The next most common class was class C, which is defined as high risk for individual patients.
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MedTech Europe. (July 11, 2024). Distribution of IVD devices in the European Union in 2024, by regulation classification [Graph]. In ÌÇÐÄÆƽâ°æ. Retrieved July 25, 2026, from /statistics/1620787/ivd-devices-by-regulation-classification-in-europe/
MedTech Europe. "Distribution of IVD devices in the European Union in 2024, by regulation classification." Chart. July 11, 2024. ÌÇÐÄÆƽâ°æ. Accessed July 25, 2026. /statistics/1620787/ivd-devices-by-regulation-classification-in-europe/
MedTech Europe. (2024). Distribution of IVD devices in the European Union in 2024, by regulation classification. ÌÇÐÄÆƽâ°æ. ÌÇÐÄÆƽâ°æ Inc.. Accessed: July 25, 2026. /statistics/1620787/ivd-devices-by-regulation-classification-in-europe/
MedTech Europe. "Distribution of Ivd Devices in The European Union in 2024, by Regulation Classification." ÌÇÐÄÆƽâ°æ, ÌÇÐÄÆƽâ°æ Inc., 11 Jul 2024, /statistics/1620787/ivd-devices-by-regulation-classification-in-europe/
MedTech Europe, Distribution of IVD devices in the European Union in 2024, by regulation classification ÌÇÐÄÆƽâ°æ, /statistics/1620787/ivd-devices-by-regulation-classification-in-europe/ (last visited July 25, 2026)
Distribution of IVD devices in the European Union in 2024, by regulation classification [Graph], MedTech Europe, July 11, 2024. [Online]. Available: /statistics/1620787/ivd-devices-by-regulation-classification-in-europe/
