Taiwan FDA registration 72807359b52d5ca7bdf21ba86a7bce4a
Klux Automated External Defibrillator
TW: 凱樂斯自動體外心臟去顫電擊器
Taiwan·Risk Class 3·MD·KLUX CO., LTD.·Registered Sep 15, 2015 – Sep 15, 2025ExpiredRegistration details
- Analysis ID
- 72807359b52d5ca7bdf21ba86a7bce4a
- License Form
- Ministry of Health Medical Device Manufacturing No. 005119
Company information
- Manufacturer
- KLUX CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- KLUX 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
- Produced in Taiwan, China
Dates and status
- Registration Date
- Sep 15, 2015
- Expiry Date
- Sep 15, 2025
About this record
Access comprehensive regulatory information for Klux Automated External Defibrillator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 72807359b52d5ca7bdf21ba86a7bce4a and manufactured by KLUX CO., LTD.. The authorized representative in Taiwan is KLUX CO., LTD..
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