"Carnega" Fotis coronary angioplasty catheter
Taiwan·Risk Class 2·KANEKA MEDIX CORPORATION KANAGAWA PLANT·Registered Aug 27, 2007 – Aug 27, 2022Cancelled- Analysis ID
- ad1bb43038b76f428e4da3aca603fc66
- Customs Code
- DHA00601822300
- 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
- Aug 27, 2007
- Expiry Date
- Aug 27, 2022
- Cancellation Date
- Apr 12, 2024
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Carnega" Fotis coronary angioplasty catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ad1bb43038b76f428e4da3aca603fc66 and manufactured by KANEKA MEDIX CORPORATION KANAGAWA PLANT. The authorized representative in Taiwan is HSIN TUNG MEDICAL CO., LTD..
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