Taiwan FDA registration 122e6fb4c4fa8b1c5624cff36d32747f

"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 14, 2020 – Feb 14, 2030Active
Registration details
Analysis ID
122e6fb4c4fa8b1c5624cff36d32747f
Customs Code
DHA05603323908
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 14, 2020
Expiry Date
Feb 14, 2030
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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 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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