Taiwan FDA registration 7b1b7569aef18cc16d3f51361221095c
"Biosen Webster" Webster 20-pole electrophysiological catheter
TW: “百歐森偉伯司特”偉伯司特二十極電生理導管
Taiwan·Risk Class 2·Biosense Webster, Inc.·Registered Dec 28, 2020 – Dec 28, 2025ExpiredRegistration details
- Analysis ID
- 7b1b7569aef18cc16d3f51361221095c
- Customs Code
- DHA05603423202
Company information
- Manufacturer
- Biosense Webster, Inc.
- 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.1220 電極記錄導管或電極記錄探頭
- Import Information
- import
Dates and status
- Registration Date
- Dec 28, 2020
- Expiry Date
- Dec 28, 2025
About this record
Access comprehensive regulatory information for "Biosen Webster" Webster 20-pole electrophysiological catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7b1b7569aef18cc16d3f51361221095c 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