Taiwan FDA registration 70d240f6d8d49b7ae4d167cdd27db6fd
“Nihon Kohden” Cardiolife Defibrillator Pads
TW: “日本光電”心臟除顫器用電擊貼片
Taiwan·Risk Class 2·MD·Nihon Kohden Kawamoto Production Center·Registered Nov 06, 2017 – Nov 06, 2027ActiveRegistration details
- Analysis ID
- 70d240f6d8d49b7ae4d167cdd27db6fd
- License Form
- Ministry of Health Medical Device Import No. 030413
- Customs Code
- DHA05603041309
Company information
- Manufacturer
- Nihon Kohden Kawamoto Production Center
- 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)
- E5300 DC Defibrillator (with shock plate)
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 06, 2017
- Expiry Date
- Nov 06, 2027
About this record
Access comprehensive regulatory information for “Nihon Kohden” Cardiolife Defibrillator Pads in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 70d240f6d8d49b7ae4d167cdd27db6fd and manufactured by Nihon Kohden Kawamoto Production Center. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..
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