Taiwan FDA registration a31572b6e3c403c41d5ef256ff9267e5
"Kennett" powered therapy unit (unsterilized)
TW: “肯尼特”動力式治療檯 (未滅菌)
Taiwan·Risk Class 1·KINETEC S.A.·Registered Feb 26, 2009 – Feb 26, 2014CancelledRegistration details
- Analysis ID
- a31572b6e3c403c41d5ef256ff9267e5
- Customs Code
- DHA04400751904
Company information
- Manufacturer
- KINETEC S.A.
- Manufacturer Country
- France
- Authorized Representative
- Yajin International Limited
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Powered Treatment Units (O.3760)".
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.3760 Powered therapy cage
- Import Information
- import
Dates and status
- Registration Date
- Feb 26, 2009
- Expiry Date
- Feb 26, 2014
- Cancellation Date
- Jan 09, 2017
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Kennett" powered therapy unit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a31572b6e3c403c41d5ef256ff9267e5 and manufactured by KINETEC S.A.. The authorized representative in Taiwan is Yajin International Limited.
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