🎉 #采風智匯 #退化性關節炎AI判讀軟體 獲 #TFDA #FDA 雙認證
AIM is pleased to announce that its DeepXrayTM AI-assisted diagnosis system for prevailing chronic bone diseases has received FDA 510(k) clearance (Class II medical device). Along with 2 TFDA approvals, QMS and ISO 13485 certificates obtained recently, AIM is expecting to enter into a high growth stage in the coming 2024.
采風智匯(AIM)旗下產品 DeepXray™ 骨骼慢性疾病AI診斷輔助系統,九月初經美國食品藥物管理局(FDA)審核通過,取得AI輔助診斷之510k上市許可(Class II醫材)。加上今年稍早取得的兩張TFDA、及QMS與ISO 1348認證,預期將會為采風智慧的成長提供強大驅動力。
🌎 完整報導
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