Taiwan FDA registration bea069ed8949529a7f89c638b71a1969
"Biosen Webster" Webster automatically identifies fixed curved electrophysiological catheters
TW: “百歐森偉伯斯特”偉伯司特自動辨識固定彎式電生理導管
Taiwan·Risk Class 2·BIOSENSE WEBSTER, INC.·Registered Aug 06, 2012 – Aug 06, 2017CancelledRegistration details
- Analysis ID
- bea069ed8949529a7f89c638b71a1969
- Customs Code
- DHA00602391701
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 06, 2012
- Expiry Date
- Aug 06, 2017
- Cancellation Date
- Nov 04, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Biosen Webster" Webster automatically identifies fixed curved 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 bea069ed8949529a7f89c638b71a1969 and manufactured by BIOSENSE WEBSTER, INC.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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