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)
CosmoDerm Human-Based Collagen Implant CosmoDerm Human-Based Collagen Implant 利民生技有限公司ptt Uriscan “洋克美克”舒膜墊水膠體繃帶 (未滅菌) 明基三豐醫療器材股份有限公司臺中廠 明基三豐醫療口罩 針筒屈臣氏 胰島素專用塑膠注射筒附針 CLIA Lab
SUMMARY OF SAFETY AND EFFECTIVENESS DATA | 合法醫療器材資訊網
Inamed CosmoDermTM Human | 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
Cosmoderm® and CosmoPlast® Human | 合法醫療器材資訊網
Cosmoderm® and CosmoPlast® Human | 合法醫療器材資訊網
CosmoDermCosmoPlast (Human Bioengineered Collagen ... | 合法醫療器材資訊網
可賜美得萌人類膠原蛋白植入劑CosmoDerm Human | 合法醫療器材資訊網
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【可賜美得萌人類膠原蛋白植入劑】許可證字號:衛署醫器輸字第017218號
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