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The nmpa requires clinical data for all class ii and class iii devices, unless the device appears in one of the regulator’s published clinical evaluation exemption lists. 中国国家薬品監督管理局＜national medical products administration (nmpa)> であり、中国で販売するすべての医療機器、医薬品、医薬品包材、化粧品、保健食品の審査認.
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