Taiwan FDA registration 6af1f1e4d5731c4086c0247d6a0faaf1
"Biosen Webster" has a navigable catheter
TW: “百歐森偉伯司特”得可導航導管
Taiwan·Risk Class 2·Biosense Webster, Inc.;; Biosense Webster Inc.·Registered Dec 17, 2013 – Dec 17, 2028ActiveRegistration details
- Analysis ID
- 6af1f1e4d5731c4086c0247d6a0faaf1
- Customs Code
- DHA05602566605
Company information
- Manufacturer
- Biosense Webster, Inc.;; Biosense Webster Inc.
- Manufacturer Country
- 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 17, 2013
- Expiry Date
- Dec 17, 2028
About this record
Access comprehensive regulatory information for "Biosen Webster" has a navigable catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6af1f1e4d5731c4086c0247d6a0faaf1 and manufactured by Biosense Webster, Inc.;; 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