Taiwan FDA registration a5593ea8742f6bb8425dd39b54e878ee
"Ashstan" cannula guide strip (unsterilized)
TW: “亞仕丹”插管導引探條 (未滅菌)
Taiwan·Risk Class 1·Xubang Medical Equipment Co., Ltd·Registered May 13, 2008 – May 13, 2018CancelledRegistration details
- Analysis ID
- a5593ea8742f6bb8425dd39b54e878ee
Company information
- Manufacturer
- Xubang Medical Equipment Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BIOTRONIC INSTRUMENT ENTERPRISE LTD.
Product details
- Intended Use
- Limited to the first level identification range of the endotracheal tube probe difference (D.5790) of the Medical Device Management Measures.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5790 氣管內管探針
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- May 13, 2008
- Expiry Date
- May 13, 2018
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Ashstan" cannula guide strip (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a5593ea8742f6bb8425dd39b54e878ee and manufactured by Xubang Medical Equipment Co., Ltd. The authorized representative in Taiwan is BIOTRONIC INSTRUMENT ENTERPRISE LTD..
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