"Shengyoda" through the middle diaphragm duct system - Taiwan Registration 51a29d87ae0aab7a7b1a6a7f7c18eff6
Access comprehensive regulatory information for "Shengyoda" through the middle diaphragm duct system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 51a29d87ae0aab7a7b1a6a7f7c18eff6 and manufactured by ST. JUDE MEDICAL. The authorized representative in Taiwan is Taiwan Shengyuda Medical Supplies 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.1340 ๅฐ็ฎกๅฐๅผๅจ;; E.1390 ๅฅ็ฎก้
import
Dates and Status
Jul 09, 2008
Jul 09, 2018
Jul 15, 2022
Cancellation Information
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