Taiwan FDA registration bf098ce3dad543464a602fbfa9ea6836
“Acare” CPAP system
TW: “眾里”陽壓呼吸器
Taiwan·Risk Class 2·MD·The second factory of Zhongli Technology Co., Ltd·Registered Apr 30, 2014 – Apr 30, 2024ExpiredRegistration details
- Analysis ID
- bf098ce3dad543464a602fbfa9ea6836
- License Form
- Ministry of Health Medical Device Manufacturing No. 004580
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)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5895 Continuous breathing apparatus
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Apr 30, 2014
- Expiry Date
- Apr 30, 2024
About this record
Access comprehensive regulatory information for “Acare” CPAP system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bf098ce3dad543464a602fbfa9ea6836 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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