Taiwan FDA registration 4879d3d014241149e03c8e62dec53388
"Taiwan Biomedical Doctor" tracheal tubing fixation device (unsterilized)
TW: "台灣生醫" 氣管管路固定裝置 (未滅菌)
Taiwan·Risk Class 1·TUNGSHI MEDICAL EQUIPMENT CO., LTD.·Registered Mar 19, 2012 – Mar 19, 2017CancelledRegistration details
- Analysis ID
- 4879d3d014241149e03c8e62dec53388
Company information
- Manufacturer
- TUNGSHI MEDICAL EQUIPMENT CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Taiwan Biomedical Engineering Co., Ltd
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Tracheal Pipeline Fixation Device (D.5770)".
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5770 氣管管路固定裝置
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Mar 19, 2012
- Expiry Date
- Mar 19, 2017
- Cancellation Date
- Jan 06, 2020
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Taiwan Biomedical Doctor" tracheal tubing fixation device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4879d3d014241149e03c8e62dec53388 and manufactured by TUNGSHI MEDICAL EQUIPMENT CO., LTD.. The authorized representative in Taiwan is Taiwan Biomedical Engineering Co., Ltd.
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