Taiwan FDA registration 610f9105df80ad6f2b6ecc7ccfac7f18
"Kaneka" Ray quickly withdraws a coronary balloon catheter
TW: “卡內卡”雷快速抽換冠狀動脈氣球導管
Taiwan·Risk Class 3·KANEKA MEDIX CORPORATION KANAGAWA PLANT·Registered Dec 05, 2008 – Dec 05, 2018CancelledRegistration details
- Analysis ID
- 610f9105df80ad6f2b6ecc7ccfac7f18
- Customs Code
- DHA00601949206
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.0005.
- Import Information
- import
Dates and status
- Registration Date
- Dec 05, 2008
- Expiry Date
- Dec 05, 2018
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Kaneka" Ray quickly withdraws a coronary balloon catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 610f9105df80ad6f2b6ecc7ccfac7f18 and manufactured by KANEKA MEDIX CORPORATION KANAGAWA PLANT. The authorized representative in Taiwan is HSIN TUNG MEDICAL CO., LTD..
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