Premarket Approval (PMA) | 合法醫療器材資訊網
Premarket approval (PMA) is the FDA process of scientific and regulatory review to evaluate the safety and effectiveness of Class III medical devices. Class III devices are those that support or sustain human life, are of substantial importance in preventing impairment of human health, or which present a potential, unreasonable risk of illness or injury.
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References Learn more... (www.fda.gov)
"SCIMED" PTA CATHETER "SCIMED" PTA CATHETER Medtronic catheter “飛利浦”磁振造影系統 blink冰藍高水份隱形眼鏡潤濕液 星辰血壓計715 星辰手臂式電子血壓計chd701 citizen血壓計說明書 “愛力根”娜綺麗音斯蓓拉矽膠乳房植入物
Class 2 Device Recall Boston Scientific Scimed | 合法醫療器材資訊網
Premarket Approval (PMA) | 合法醫療器材資訊網
Scimed Life Systems Inc FDA Filings | 合法醫療器材資訊網
US4838269A | 合法醫療器材資訊網
必利勁怎麽服用達到治療效果 | 合法醫療器材資訊網
經皮穿刺末稍血管整形導管"SCIMED" PTA CATHETER ... | 合法醫療器材資訊網
經皮穿刺末稍血管整形導管"SCIMED" PTA CATHETER} | 合法醫療器材資訊網
經皮穿刺末稍血管整形導管"SCIMED" PTA CATHETER} | 合法醫療器材資訊網
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