Taiwan FDA registration 133637150d72fb39bbdb171e30e306b5

Defibrillation catheter

TW: 去纖維顫動導管
Taiwan flagTaiwan·MEDTRONIC INC.·Registered Jan 03, 1997 – Jan 03, 2007Cancelled
Registration details
Analysis ID
133637150d72fb39bbdb171e30e306b5
Customs Code
DHA00600811504
Company information
Manufacturer
MEDTRONIC INC.
Manufacturer Country
United States
Authorized Representative
Taiwan Medtronic Dingzhong Co., Ltd
Product details
Product Type (Level 1)
0300 Prosthetic function substitute
Import Information
import
Dates and status
Registration Date
Jan 03, 1997
Expiry Date
Jan 03, 2007
Cancellation Date
Nov 06, 2012
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for Defibrillation catheter in Taiwan's medical device market through Pure Global AI's free database. is registered under number 133637150d72fb39bbdb171e30e306b5 and manufactured by MEDTRONIC INC.. The authorized representative in Taiwan is Taiwan Medtronic Dingzhong Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including Boston Scientific Corporation, BOSTON SCIENTIFIC DE COSTA RICA, S.R.L., and 5 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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