"Carneca" percutaneous puncture of the coronary ductus
- Analysis ID
- fb56eee5b427b1c81da55b9c161f2dbe
- Customs Code
- DHA05602969802
- Manufacturer Country
- Japan
- Authorized Representative
- QUALTECH CONSULTING CORPORATION
- 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
- May 11, 2017
- Expiry Date
- May 11, 2027
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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 2 medical device is registered under number fb56eee5b427b1c81da55b9c161f2dbe and manufactured by KANEKA CORPORATION;; KANEKA CORPORATION OSAKA PLANT. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including KANEKA MEDIX CORPORATION KANAGAWA PLANT, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.