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MDCG 2021-24 - Guidance on classification of medical devices
- https://health.ec.europa.eu/latest-updates/mdcg-2021-24-guidance-classification-medical-devices-2021-10-04_en
- MDCG 2021-24 - Guidance on classification of medical devices 1 DECEMBER 2021 mdcg_2021-24_en.pdf English (1.52 MB - PDF) Download Details Publication date 4 October 2021 Author Directorate-General for Health and Food Safety …
Medical devices | European Medicines Agency
- https://www.ema.europa.eu/en/human-regulatory/overview/medical-devices
- The Medical Devices Regulation applies since 26 May 2021. Manufacturers must comply with the Regulation when placing new medical devices on the market. It …
Classify Your Medical Device | FDA
- https://www.fda.gov/medical-devices/overview-device-regulation/classify-your-medical-device
- Each classification panel in the CFR begins with a list of devices classified in that panel. Each classified device has a 7-digit number associated with it, e.g., 21 CFR 880.2920 - …
Overview of Medical Device Classification and …
- https://www.fda.gov/about-fda/cdrh-transparency/overview-medical-device-classification-and-reclassification
- The FDA categorizes medical devices into one of three classes – Class I, II, or III – based on their risks and the regulatory controls necessary to provide a reasonable assurance of …
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