"Clear stream" Qingpai European-American plus percutaneous puncture angioplasty catheter - Taiwan Registration 5820212732ac611c6cd1555ca99f6d8d
Access comprehensive regulatory information for "Clear stream" Qingpai European-American plus percutaneous puncture 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 5820212732ac611c6cd1555ca99f6d8d and manufactured by CLEARSTREAM TECHNOLOGIES LTD.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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.1250 Percutaneous catheters
import
Dates and Status
Nov 08, 2012
Nov 08, 2017
Dec 20, 2019
Cancellation Information
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