"Carnega" Fotis coronary angioplasty catheter - Taiwan Registration ad1bb43038b76f428e4da3aca603fc66
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 2 medical device is registered under number ad1bb43038b76f428e4da3aca603fc66 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
Aug 27, 2007
Aug 27, 2022
Apr 12, 2024
Cancellation Information
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