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)
"DEPUY SPINE"SABER LUMBAR I/F CAGE SYSTEM "DEPUY SPINE"SABER LUMBAR I/F CAGE SYSTEM Planmeca CBCT Romexis Viewer 杏 昌生 技 血壓計 春菖貿易有限公司ptt Ambu 公司 kowa genesis-d kowa tonometer 手術後拆
"帝富脊椎"腰椎護架系統"DEPUY SPINE"SABER LUMBAR IF ... | 合法醫療器材資訊網
"帝富脊椎"腰椎護架系統 | 合法醫療器材資訊網
DePuySynthes | 合法醫療器材資訊網
Medical Device SABER LUMBAR I F CAGE CAGE SYSTEM | 合法醫療器材資訊網
Medos International SARL Sheree Geller ... | 合法醫療器材資訊網
Medos International SARL Sheree Geller Regulatory Affairs ... | 合法醫療器材資訊網
Premarket Approval (PMA) | 合法醫療器材資訊網
Premarket Approval (PMA) | 合法醫療器材資訊網
SABER LUMBAR IF CAGE | 合法醫療器材資訊網
Strength | 合法醫療器材資訊網
相關資訊整理
【"帝富脊椎"腰椎護架系統】許可證字號:衛署醫器輸字第017009號
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