Taiwan FDA registration 7eca7e2aff3ed3f977ef4c295d611942
"Keyun" limb equipment (unsterilized)
TW: “科云” 肢體裝具 (未滅菌)
Taiwan·Risk Class 1·Keyun Biomedical Technology Co., Ltd. Precision Factory·Registered Sep 28, 2012 – Sep 28, 2017CancelledRegistration details
- Analysis ID
- 7eca7e2aff3ed3f977ef4c295d611942
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Keyun Biomedical Technology Co., Ltd
Product details
- Intended Use
- Limited to the first level recognition range of limb equipment (O.3475) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.3475 Limb fittings
- Import Information
- Domestic
Dates and status
- Registration Date
- Sep 28, 2012
- Expiry Date
- Sep 28, 2017
- Cancellation Date
- May 21, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Keyun" limb equipment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7eca7e2aff3ed3f977ef4c295d611942 and manufactured by Keyun Biomedical Technology Co., Ltd. Precision Factory. The authorized representative in Taiwan is Keyun Biomedical Technology Co., Ltd.
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