Taiwan FDA registration 640593ae279c02a5eb84fe3bad347d63

"Biosen Webster" perfusion cooled Sifu temperature controlled bidirectional diagnostic/electrofired bendable catheter

TW: “百歐森偉伯司特”灌注冷卻式斯芙溫控雙向診斷/電燒可彎式導管
Taiwan flagTaiwan·Risk Class 3·Biosense Webster, Inc.·Registered Oct 23, 2012 – Oct 23, 2027Active
Registration details
Analysis ID
640593ae279c02a5eb84fe3bad347d63
Customs Code
DHA00602414301
Company information
Manufacturer Country
Mexico;;United States
Authorized Representative
JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
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.1200 診斷用血管內導管
Import Information
import
Dates and status
Registration Date
Oct 23, 2012
Expiry Date
Oct 23, 2027
Cancellation Date
Oct 24, 2024
About this record

Access comprehensive regulatory information for "Biosen Webster" perfusion cooled Sifu temperature controlled bidirectional diagnostic/electrofired bendable catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 640593ae279c02a5eb84fe3bad347d63 and manufactured by Biosense Webster, Inc.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..

This page provides complete technical specifications, regulatory compliance details. 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.

Free DatabasePowered by Pure Global AI89,000+ Devices