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"Boston Tech" Internellue defibrillation catheter - Taiwan Registration 122e6fb4c4fa8b1c5624cff36d32747f

Access comprehensive regulatory information for "Boston Tech" Internellue defibrillation catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 122e6fb4c4fa8b1c5624cff36d32747f and manufactured by Boston Scientific Corporation. The authorized representative in Taiwan is Dutch Boston Technology Co., Ltd. Taiwan Branch.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Boston Scientific Corporation, and 1 recent registrations in the same category. 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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122e6fb4c4fa8b1c5624cff36d32747f
Registration Details
Taiwan FDA Registration: 122e6fb4c4fa8b1c5624cff36d32747f
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Device Details

"Boston Tech" Internellue defibrillation catheter
TW: โ€œๆณขๅฃซ้ “็ง‘ๆŠ€โ€ๅ› ็‰นๆ‹‰ๅฅˆ่Š™้™ค้กซๅฐŽ็ฎก
Risk Class 3

Registration Details

122e6fb4c4fa8b1c5624cff36d32747f

DHA05603323908

Company Information

Costa Rica;;United States

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

E.0008.

import

Dates and Status

Feb 14, 2020

Feb 14, 2030

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