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Medical Devices

Medical devices by brand, diagnostic testing, indications, technologies, diagnostics, therapeutic or surgical applications, and end user groups. Device classification (U.S. and Europe – Class I, II, III, and IV) and device regulatory approvals (U.S. FDA – 510(k) premarket notification, premarket approvals (PMA), humanitarian device exemption (HDE) for humanitarian use devices (HUD); and Europe – CE mark).

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