"Carneka" Coronary artery percutaneous perforated catheter - Taiwan Registration d21530681a40a6ea55864d35ab1580ca
Access comprehensive regulatory information for "Carneka" Coronary artery percutaneous perforated catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d21530681a40a6ea55864d35ab1580ca and manufactured by KANEKA MEDIX CORPORATION KANAGAWA PLANT. The authorized representative in Taiwan is HSIN TUNG MEDICAL CO., LTD..
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Device Details
Product Details
For details, it is Chinese approved copy of the imitation order
E Cardiovascular Medicine Science
E.1250 Percutaneous catheters
import
Dates and Status
Sep 30, 2005
Sep 30, 2015
Jun 26, 2018
Cancellation Information
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