"Carneca" percutaneous puncture of the coronary ductus - Taiwan Registration d4620e51df8c5909296e7ccc5780135d
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..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including KANEKA CORPORATION;; KANEKA CORPORATION OSAKA 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.
Device Details
Product Details
For details, it is Chinese approved copy of the imitation order
E Cardiovascular Medicine Science
E.0005.
import
Dates and Status
Jul 28, 2006
Jul 28, 2016
Jun 26, 2018
Cancellation Information
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