Taiwan FDA registration c2ce7224d8b7e7b698b1e5c0f11ad1c5
"Biosen Webster" Webster automatically identifies bendable electrophysiological catheters
TW: “百歐森偉伯斯特”偉伯司特自動辨識可彎式電生理導管
Taiwan·Risk Class 2·Biosense Webster, Inc.·Registered Aug 15, 2012 – Aug 15, 2027CancelledRegistration details
- Analysis ID
- c2ce7224d8b7e7b698b1e5c0f11ad1c5
- Customs Code
- DHA00602392602
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.1220 電極記錄導管或電極記錄探頭
- Import Information
- import
Dates and status
- Registration Date
- Aug 15, 2012
- Expiry Date
- Aug 15, 2027
- Cancellation Date
- Aug 17, 2023
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Biosen Webster" Webster automatically identifies bendable electrophysiological catheters in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c2ce7224d8b7e7b698b1e5c0f11ad1c5 and manufactured by Biosense Webster, Inc.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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