Taiwan FDA registration df80f612c7faaa315dce1173861bf7e3
"Aon" tubing fixture (unsterilized)
TW: "怡安" 氣管管路固定裝置 (未滅菌)
Taiwan·Risk Class 1·HANGZHOU SHANYOU MEDICAL EQUIPMENT CO., LTD·Registered Mar 22, 2011 – Mar 22, 2016CancelledRegistration details
- Analysis ID
- df80f612c7faaa315dce1173861bf7e3
- Customs Code
- DHA04600130701
Company information
- Manufacturer
- HANGZHOU SHANYOU MEDICAL EQUIPMENT CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- LILY MEDICAL CORPORATION
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
- Chinese goods;; input
Dates and status
- Registration Date
- Mar 22, 2011
- Expiry Date
- Mar 22, 2016
- Cancellation Date
- May 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Aon" tubing fixture (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number df80f612c7faaa315dce1173861bf7e3 and manufactured by HANGZHOU SHANYOU MEDICAL EQUIPMENT CO., LTD. The authorized representative in Taiwan is LILY MEDICAL CORPORATION.
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