Taiwan FDA registration d21530681a40a6ea55864d35ab1580ca
"Carneka" Coronary artery percutaneous perforated catheter
TW: "卡內卡" 冠狀動脈經皮穿通導管
Taiwan·Risk Class 2·KANEKA MEDIX CORPORATION KANAGAWA PLANT·Registered Sep 30, 2005 – Sep 30, 2015CancelledRegistration details
- Analysis ID
- d21530681a40a6ea55864d35ab1580ca
- Customs Code
- DHA00601252104
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
- Sep 30, 2005
- Expiry Date
- Sep 30, 2015
- Cancellation Date
- Jun 26, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Carneka" Coronary artery percutaneous perforated catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d21530681a40a6ea55864d35ab1580ca and manufactured by KANEKA MEDIX CORPORATION KANAGAWA PLANT. The authorized representative in Taiwan is HSIN TUNG MEDICAL CO., LTD..
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