"Boston Tech" Stinger defibrillation electrode catheter - Taiwan Registration 5504a51f77f4ac21743102037d75d23d
Access comprehensive regulatory information for "Boston Tech" Stinger defibrillation electrode catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 5504a51f77f4ac21743102037d75d23d and manufactured by Boston Scientific Corporation;; C.R. BARD, INC.. The authorized representative in Taiwan is Dutch Boston Technology Co., Ltd. Taiwan Branch.
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.
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5504a51f77f4ac21743102037d75d23d
Registration Details
Taiwan FDA Registration: 5504a51f77f4ac21743102037d75d23d
Device Details
"Boston Tech" Stinger defibrillation electrode catheter
TW: โๆณขๅฃซ้ ็งๆโ ๅฒๆฑๆ ผ้ค้กซ้ปๆฅตๅฐ็ฎก
Risk Class 3
Cancelled

