Taiwan FDA registration 0a41c90615c06be99912d0c51e047e1f
"Bayerson" kinetic source line coronary balloon dilation catheter
TW: “拜爾生”動源線冠狀動脈氣球擴張導管
Taiwan·Risk Class 3·BIOSENSORS INTERVENTIONAL TECHNOLOGIES PTE LTD.·Registered Feb 19, 2009 – Feb 19, 2014CancelledRegistration details
- Analysis ID
- 0a41c90615c06be99912d0c51e047e1f
- Customs Code
- DHA00601966501
Company information
- Manufacturer
- BIOSENSORS INTERVENTIONAL TECHNOLOGIES PTE LTD.
- Manufacturer Country
- Singapore
- Authorized Representative
- KINGDOM EAST ENTERPRISE CO., LTD.
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.0005.
- Import Information
- import
Dates and status
- Registration Date
- Feb 19, 2009
- Expiry Date
- Feb 19, 2014
- Cancellation Date
- Nov 15, 2016
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Bayerson" kinetic source line coronary balloon dilation catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 0a41c90615c06be99912d0c51e047e1f and manufactured by BIOSENSORS INTERVENTIONAL TECHNOLOGIES PTE LTD.. The authorized representative in Taiwan is KINGDOM EAST ENTERPRISE CO., LTD..
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