Taiwan FDA registration b0b0bf18afafc818c6b192f20044d912
"Biosen Webster" Cadofiseo double guide sheath tube
TW: “百歐森偉伯司特”卡多費斯歐雙向導引鞘管
Taiwan·Risk Class 2·Biosense Webster, Inc.·Registered Apr 29, 2020 – Apr 29, 2025ExpiredRegistration details
- Analysis ID
- b0b0bf18afafc818c6b192f20044d912
- Customs Code
- DHA05603357501
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)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1340 Catheter Introducers
- Import Information
- import
Dates and status
- Registration Date
- Apr 29, 2020
- Expiry Date
- Apr 29, 2025
About this record
Access comprehensive regulatory information for "Biosen Webster" Cadofiseo double guide sheath tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b0b0bf18afafc818c6b192f20044d912 and manufactured by Biosense Webster, Inc.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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