"Carnega" Fotis coronary angioplasty catheter
Taiwan·Risk Class 3·KANEKA MEDIX CORPORATION KANAGAWA PLANT·Registered Nov 06, 2006 – Nov 06, 2011Cancelled- Analysis ID
- 99b01b5283bb9a369f3969b2fe05aec2
- Customs Code
- DHA00601740501
- 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
- Nov 06, 2006
- Expiry Date
- Nov 06, 2011
- Cancellation Date
- Nov 09, 2012
- 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 3 medical device is registered under number 99b01b5283bb9a369f3969b2fe05aec2 and manufactured by KANEKA MEDIX CORPORATION KANAGAWA PLANT. The authorized representative in Taiwan is HSIN TUNG MEDICAL CO., LTD..
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