"Parkson" percutaneous coronary angioplasty balloon catheter - Taiwan Registration 2f0cb7f5276ad731736395303c0aeafb
Access comprehensive regulatory information for "Parkson" percutaneous coronary angioplasty balloon catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 2f0cb7f5276ad731736395303c0aeafb and manufactured by BIOSENSORS INTERVENTIONAL TECHNOLOGIES PTE LTD.. The authorized representative in Taiwan is IDS MEDICAL SYSTEMS (HONG KONG) COMPANY LIMITED, TAIWAN BRANCH (HONG KONG).
This page provides complete technical specifications, regulatory compliance details. 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 03, 2009
Nov 03, 2019
Jun 07, 2022
Cancellation Information
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