Taiwan FDA registration bc433a95d86681f5cb5f02e234f8e8b0
“Acare” Continuous Positive Airway Pressure Units (CPAP)
TW: “眾里”連續性陽壓呼吸器
Taiwan·Risk Class 2·MD·The second factory of Zhongli Technology Co., Ltd·Registered Dec 04, 2015 – Dec 04, 2020CancelledRegistration details
- Analysis ID
- bc433a95d86681f5cb5f02e234f8e8b0
- License Form
- Ministry of Health Medical Device Manufacturing No. 005217
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- ACARE TECHNOLOGY CO., LTD.
Product details
- 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
- Dec 04, 2015
- Expiry Date
- Dec 04, 2020
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “Acare” Continuous Positive Airway Pressure Units (CPAP) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bc433a95d86681f5cb5f02e234f8e8b0 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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