Taiwan FDA registration da08d6161c58183af7c4765fc2843d87
“BioCARE” Breathing circuit bacterial filter
TW: “喬聯”呼吸管路細菌過濾器
Taiwan·Risk Class 2·MD·Qiaolian Technology Co., Ltd. Nankan Factory·Registered Jun 26, 2014 – Jun 26, 2019CancelledRegistration details
- Analysis ID
- da08d6161c58183af7c4765fc2843d87
- License Form
- Ministry of Health Medical Device Manufacturing No. 004630
Company information
- Manufacturer
- Qiaolian Technology Co., Ltd. Nankan Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BIOCARE CORPORATION
Product details
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5260 Breathing line bacterial filter
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jun 26, 2014
- Expiry Date
- Jun 26, 2019
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “BioCARE” Breathing circuit bacterial filter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number da08d6161c58183af7c4765fc2843d87 and manufactured by Qiaolian Technology Co., Ltd. Nankan Factory. The authorized representative in Taiwan is BIOCARE CORPORATION.
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