Taiwan FDA registration 05df76ade6597623935f0824f660a6b9
“Acare” Suction Unit
TW: “眾里”交直流兩用抽痰機
Taiwan·Risk Class 2·MD·The second factory of Zhongli Technology Co., Ltd·Registered Mar 21, 2017 – Mar 21, 2027ActiveRegistration details
- Analysis ID
- 05df76ade6597623935f0824f660a6b9
- License Form
- Ministry of Health Medical Device Manufacturing No. 005710
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- ACARE TECHNOLOGY CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4780 powered suction pump
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Mar 21, 2017
- Expiry Date
- Mar 21, 2027
About this record
Access comprehensive regulatory information for “Acare” Suction Unit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 05df76ade6597623935f0824f660a6b9 and manufactured by The second factory of Zhongli Technology Co., Ltd. The authorized representative in Taiwan is ACARE TECHNOLOGY CO., LTD..
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