"Carnega" Fotis coronary angioplasty catheter - Taiwan Registration 99b01b5283bb9a369f3969b2fe05aec2
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..
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.
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
Nov 06, 2006
Nov 06, 2011
Nov 09, 2012
Cancellation Information
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