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“Nihon Kohden” Automated External Defibrillator AED-3100 cardiolife AED - Taiwan Registration fca619b4856988b4756bdc7547864baa

Access comprehensive regulatory information for “Nihon Kohden” Automated External Defibrillator AED-3100 cardiolife AED in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number fca619b4856988b4756bdc7547864baa and manufactured by Nihon Kohden Tomioka Corporation Tomioka Production Center. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..

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fca619b4856988b4756bdc7547864baa
Registration Details
Taiwan FDA Registration: fca619b4856988b4756bdc7547864baa
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Device Details

“Nihon Kohden” Automated External Defibrillator AED-3100 cardiolife AED
TW: “日本光電”自動體外除顫器
Risk Class 3
MD

Registration Details

fca619b4856988b4756bdc7547864baa

Ministry of Health Medical Device Import No. 028877

DHA05602887707

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular devices

E5310 Automated External Defibrillator

Imported from abroad

Dates and Status

Oct 26, 2016

Oct 26, 2026