“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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Device Details
Registration Details
fca619b4856988b4756bdc7547864baa
Ministry of Health Medical Device Import No. 028877
DHA05602887707
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

