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"Boston Tech" Internellue defibrillation catheter - Taiwan Registration b789c31518e815cc01c70c1218d3c76c

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 b789c31518e815cc01c70c1218d3c76c and manufactured by Boston Scientific Corporation. The authorized representative in Taiwan is BOSTON SCIENTIFIC INTERNATIONAL B.V., TAIWAN BRANCH (NETHERLANDS).

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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b789c31518e815cc01c70c1218d3c76c
Registration Details
Taiwan FDA Registration: b789c31518e815cc01c70c1218d3c76c
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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

b789c31518e815cc01c70c1218d3c76c

DHA05603432901

Company Information

Product Details

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

E Cardiovascular Medicine Science

E.0008.

import

Dates and Status

Feb 17, 2021

Feb 17, 2026

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