Taiwan FDA registration 01955a610e3ae1923f20c4bac7d1896f
"Nippon Opto" automatic external cardiac defibrillator
TW: “日本光電”自動體外心臟除顫器
Taiwan·Risk Class 2·Nihon Kohden Tomioka Corporation Tomioka Production Center·Registered Jun 17, 2011 – Jun 17, 2026ExpiredRegistration details
- Analysis ID
- 01955a610e3ae1923f20c4bac7d1896f
- Customs Code
- DHA00602244902
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 Medicine Science
- Product Type (Level 2)
- E.5310 自動體外去顫器系統
- Import Information
- import
Dates and status
- Registration Date
- Jun 17, 2011
- Expiry Date
- Jun 17, 2026
About this record
Access comprehensive regulatory information for "Nippon Opto" automatic external cardiac defibrillator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 01955a610e3ae1923f20c4bac7d1896f 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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