Taiwan FDA registration df47d5265a26924256aaa4ddedee7599
"Carneca" vasodilator balloon catheter
TW: “卡內卡”血管擴張氣球導管
Taiwan·Risk Class 2·KANEKA MEDIX CORPORATION KANAGAWA PLANT·Registered Aug 21, 2008 – Aug 21, 2013CancelledRegistration details
- Analysis ID
- df47d5265a26924256aaa4ddedee7599
- Customs Code
- DHA00601917201
Company information
- Manufacturer
- KANEKA MEDIX CORPORATION KANAGAWA PLANT
- Manufacturer Country
- Japan
- Authorized Representative
- HSIN TUNG MEDICAL 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.1250 Percutaneous catheters
- Import Information
- import
Dates and status
- Registration Date
- Aug 21, 2008
- Expiry Date
- Aug 21, 2013
- Cancellation Date
- Jun 02, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Carneca" vasodilator balloon catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number df47d5265a26924256aaa4ddedee7599 and manufactured by KANEKA MEDIX CORPORATION KANAGAWA PLANT. The authorized representative in Taiwan is HSIN TUNG MEDICAL CO., LTD..
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