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2023/04
"TaiHao" Ti-LUNG Decision Support System approved TFDA No.007754
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2022/08
BR-Viewer (Breast Screening Solution for Automated Breast Ultrasound), BR-FHUS Smart System (Breast Screening Solution for Hand-Held Breast Ultrasound) appoved CE Mark DE/CA20/00188434
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2022/07
BU-CAD (Breast Ultrasound Lesion Computer-aided Diagnosis Decision Support System) approved TFDA No. 007651 registration license.
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2021/12
BU-CAD (Breast Ultrasound Lesion Computer-aided Diagnosis Decision Support System) approved USFDA 510K
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2021/09
BR-FHUS Smart System (Breast Screening Solution for Hand-Held Breast Ultrasound) approved China NMPA registration license.
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2021/12
BR-FHUS Smart System (Breast Screening Solution for Hand-Held Breast Ultrasound) approved Japan PMDA registration license.
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2020/12
BU-CAD (Breast Ultrasound Lesion Computer-aided Diagnosis Decision Support System) approved USFDA 510K
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2020/03
BU-CAD (Breast Ultrasound Lesion Computer-aided Diagnosis Decision Support System) clinical trials launched at Columbia University Medical Center and Virginia Polytechnic Institute and State University in the United States
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2019/11
TaiHao medical won the Bronze Award for Pharmaceutical Science & Technology Research and Development Award from MOH and Welfare-Ministry of Economic Affairs
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2018/08
Approved ISO13485:2016 Medical device quality control system standards.
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2018/05
TaiHao medical won the Medical Artificial Intelligence Pioneer Award from International Smart Medical Innovation Forum
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2018/01
BR-FHUS Smart System approved TFDA No. 005966
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2017/12
Won 2017 year Information Month Top 100 Innovative Products - Gold Award
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2017/10
BR-FHUS Smart System approved USFDA 510k license
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2017/10
BR-FHUS Smart System won 2017 year Taipei Biotechnology Awards-New Innovation Technology Award
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2017/05
BR-Viewer approved TFDA No.005760
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2017/03
Approved GMP No.1345
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2016/12
Won 13th National Innovation Award - Start-up Enterprise, Clinical Innovation and Best Industrial Benefit Award, etc.
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2016/07
Obtained Taipei City Health Bureau Manufacturing Pharmacy License
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2016/01
BR-ABUS Viewer approved USFDA 510K
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2013/10
Company founded