Taiwan FDA registration ad56c1dfb44e406f7cee8127a62fca6c
"Yuefa" AC and DC dual-purpose sputum extraction machine
TW: “悅發”交直流兩用抽痰機
Taiwan·Risk Class 2·The second factory of Zhongli Technology Co., Ltd·Registered Sep 28, 2018 – Mar 21, 2027ActiveRegistration details
- Analysis ID
- ad56c1dfb44e406f7cee8127a62fca6c
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PE & LE ENTERPRISE LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4780 動力式抽吸幫浦
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Sep 28, 2018
- Expiry Date
- Mar 21, 2027
About this record
Access comprehensive regulatory information for "Yuefa" AC and DC dual-purpose sputum extraction machine in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ad56c1dfb44e406f7cee8127a62fca6c and manufactured by The second factory of Zhongli Technology Co., Ltd. The authorized representative in Taiwan is PE & LE ENTERPRISE LTD..
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