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"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
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Device Details

"Boston Tech" Stinger defibrillation electrode catheter
TW: โ€œๆณขๅฃซ้ “็ง‘ๆŠ€โ€ ๅฒๆฑ€ๆ ผ้™ค้กซ้›ปๆฅตๅฐŽ็ฎก
Risk Class 3
Cancelled

Registration Details

5504a51f77f4ac21743102037d75d23d

DHA00601009503

Company Information

Product Details

E Cardiovascular Medicine Science

import

Dates and Status

Oct 02, 2002

Oct 02, 2022

Apr 12, 2024

Cancellation Information

Logged out

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