Taiwan FDA registration a0966baccb48d3dbd9559e0ca56e568f
"Keyun" hydrophilic wound covering (unsterilized)
TW: “科云”親水性創傷覆蓋材 (未滅菌)
Taiwan·Risk Class 1·Keyun Biomedical Technology Co., Ltd. Taichung Factory·Registered Jul 06, 2011 – Jul 06, 2016CancelledRegistration details
- Analysis ID
- a0966baccb48d3dbd9559e0ca56e568f
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Keyun Biomedical Technology Co., Ltd
Product details
- Intended Use
- Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Hydrophilic Wound Covering Materials (I.4018)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4018 親水性創傷覆蓋材
- Import Information
- Domestic
Dates and status
- Registration Date
- Jul 06, 2011
- Expiry Date
- Jul 06, 2016
- Cancellation Date
- May 08, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷;;許可證已逾有效期
About this record
Access comprehensive regulatory information for "Keyun" hydrophilic wound covering (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a0966baccb48d3dbd9559e0ca56e568f and manufactured by Keyun Biomedical Technology Co., Ltd. Taichung Factory. The authorized representative in Taiwan is Keyun Biomedical Technology Co., Ltd.
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