Taiwan FDA registration 0c24e7010ddeb17018faa07b5d92d4d4
"Biosen Webster" reservoir flow perfusion cannula set
TW: “百歐森偉伯司特”庫流灌注套管組
Taiwan·Risk Class 2·BIOSENSE WEBSTER, INC.·Registered Mar 24, 2008 – Mar 24, 2023ExpiredRegistration details
- Analysis ID
- 0c24e7010ddeb17018faa07b5d92d4d4
- Customs Code
- DHA00601874201
Company information
- Manufacturer
- 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)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5440 血管內輸液套
- Import Information
- import
Dates and status
- Registration Date
- Mar 24, 2008
- Expiry Date
- Mar 24, 2023
About this record
Access comprehensive regulatory information for "Biosen Webster" reservoir flow perfusion cannula set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0c24e7010ddeb17018faa07b5d92d4d4 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