Notice of Adverse Event Report

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The user and/or patient should report any serious incidents that have occurred in relation to the device to the manufacturer and the competent authority of the Member State in which the user and/or patient is established.

Report to manufacturer at:

Telephone: +82-02-2193-9600

Website: www.medit.com

email: support@medit.com

Report to local authority at:

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): Medical device alert

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

BfArM : Medical device alert

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

MFDS (Ministry of Food and Drug Safety) : Medical device alert

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

Japan

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


Medit Corp.

9F, 10F, 13F, 14F, 16F, 8, Yangpyeong-ro 25-gil, Yeongdeungpo-gu, Seoul, 07207, Republic of Korea

Tel: +82-02-2193-9600

Contact for Product Support

Email: support@medit.com

Tel: +82-02-2193-960