Taiwan FDA registration e17e9fb254f24c5e79a11a6c6f1aa0f8

"Boston Technologies" Breser defibrillation electrode catheter

TW: “波士頓科技”布雷瑟除顫電極導管
Taiwan flagTaiwan·Risk Class 3·BOSTON SCIENTIFIC DE COSTA RICA, S.R.L.·Registered Mar 10, 2011 – Mar 10, 2026Expired
Registration details
Analysis ID
e17e9fb254f24c5e79a11a6c6f1aa0f8
Customs Code
DHA00602208605
Company information
Manufacturer Country
Costa Rica
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
Mar 10, 2011
Expiry Date
Mar 10, 2026
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About this record

Access comprehensive regulatory information for "Boston Technologies" Breser 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 e17e9fb254f24c5e79a11a6c6f1aa0f8 and manufactured by BOSTON SCIENTIFIC DE COSTA RICA, S.R.L.. The authorized representative in Taiwan is Dutch Boston Technology Co., Ltd. Taiwan Branch.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including BOSTON SCIENTIFIC DE COSTA RICA, S.R.L., BOSTON SCIENTIFIC CORPORTAION-SAN JOSE, and 2 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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