Taiwan FDA registration fca619b4856988b4756bdc7547864baa
“Nihon Kohden” Automated External Defibrillator AED-3100 cardiolife AED
TW: “日本光電”自動體外除顫器
Taiwan·Risk Class 3·MD·Nihon Kohden Tomioka Corporation Tomioka Production Center·Registered Oct 26, 2016 – Oct 26, 2026ActiveRegistration details
- Analysis ID
- fca619b4856988b4756bdc7547864baa
- License Form
- Ministry of Health Medical Device Import No. 028877
- Customs Code
- DHA05602887707
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- K&C MEDICAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E5310 Automated External Defibrillator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 26, 2016
- Expiry Date
- Oct 26, 2026
About this record
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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