有害事象レポート通知

FDA MAUDE

http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfMAUDE/search.CFM

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm

MHRA（Medicines & Healthcare products Regulatory Agency：英国医薬品医療製品規制庁）：医療デバイスアラート

https://www.gov.uk/drug-device-alerts

BfArM（連邦医薬品医療機器研究所）：医療デバイスアラート

https://www.bfarm.de/SiteGlobals/Forms/Suche/EN/kundeninfo_Filtersuche_Formular_en.html

MFDS（食品医薬品安全処）：医療デバイスアラート

http://www.mfds.go.kr/brd/m_548/list.do

https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm

European_EUDAMED

https://ec.europa.eu/tools/eudamed/#/screen/search-device

Australia

https://apps.tga.gov.au/prod/mdir/mdirsummary.aspx?sid=new

Canada

https://www.canada.ca/en/health-canada/services/drugs-health-products/medeffect-canada/adverse-reaction-reporting.html

Brazil

https://notivisa.anvisa.gov.br/frmLogin.asp

日本

https://www.estrigw.pmda.go.jp/Iryo/Login/Index?ReturnUrl=%2fIryo

Taiwan

https://qms.fda.gov.tw/tcbw/main/ap/index.jsp

Switzerland

https://www.swissmedic.ch/swissmedic/en/home/medical-devices/reporting-incidents---fscas/users---operators.html