"Carneca" percutaneous puncture of the coronary ductus
Taiwan·Risk Class 3·KANEKA MEDIX CORPORATION KANAGAWA PLANT·Registered Jul 28, 2006 – Jul 28, 2016Cancelled- Analysis ID
- d4620e51df8c5909296e7ccc5780135d
- Customs Code
- DHA00601692509
- Manufacturer
- KANEKA MEDIX CORPORATION KANAGAWA PLANT
- Manufacturer Country
- Japan
- Authorized Representative
- HSIN TUNG MEDICAL CO., LTD.
- 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
- Registration Date
- Jul 28, 2006
- Expiry Date
- Jul 28, 2016
- Cancellation Date
- Jun 26, 2018
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Carneca" percutaneous puncture of the coronary ductus in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number d4620e51df8c5909296e7ccc5780135d and manufactured by KANEKA MEDIX CORPORATION KANAGAWA PLANT. The authorized representative in Taiwan is HSIN TUNG MEDICAL CO., LTD..
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