Taiwan FDA registration fef9c8de41417c00c8d35483d2e6c150
"Kentley" compression system
TW: “肯特利”壓縮系統
Taiwan·Risk Class 2·KENDALL, A DIVISION OF TYCO HEALTHCARE GROUP LP·Registered May 20, 2009 – May 20, 2014CancelledRegistration details
- Analysis ID
- fef9c8de41417c00c8d35483d2e6c150
- Customs Code
- DHA00601986802
Company information
- Manufacturer
- KENDALL, A DIVISION OF TYCO HEALTHCARE GROUP LP
- Manufacturer Country
- United States
- Authorized Representative
- Taiwan Covidien Corporation Limited
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.5800 Compression sleeves for limbs
- Import Information
- import
Dates and status
- Registration Date
- May 20, 2009
- Expiry Date
- May 20, 2014
- Cancellation Date
- Mar 16, 2017
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "Kentley" compression system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fef9c8de41417c00c8d35483d2e6c150 and manufactured by KENDALL, A DIVISION OF TYCO HEALTHCARE GROUP LP. The authorized representative in Taiwan is Taiwan Covidien Corporation Limited.
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