Taiwan FDA registration b789c31518e815cc01c70c1218d3c76c

"Boston Tech" Internellue defibrillation catheter

TW: “波士頓科技” 因特拉奈芙除顫導管
Taiwan flagTaiwan·Risk Class 3·Boston Scientific Corporation·Registered Feb 17, 2021 – Feb 17, 2026Expired
Registration details
Analysis ID
b789c31518e815cc01c70c1218d3c76c
Customs Code
DHA05603432901
Company information
Manufacturer Country
Costa Rica;;United States
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
E Cardiovascular Medicine Science
Product Type (Level 2)
E.0008.
Import Information
import
Dates and status
Registration Date
Feb 17, 2021
Expiry Date
Feb 17, 2026
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About this record

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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