Taiwan FDA registration 9dad7430347f3bb995cba3b9b87286c7
“Biosense Webster” nMARQ Multi-Channel RF Generator
TW: “百歐森偉伯斯特”安瑪可多通道心臟射頻電燒儀
Taiwan·Risk Class 3·MD·BIOSENSE WEBSTER, INC.·Registered Nov 11, 2015 – Nov 11, 2020CancelledRegistration details
- Analysis ID
- 9dad7430347f3bb995cba3b9b87286c7
- License Form
- Ministry of Health Medical Device Import No. 027847
- Customs Code
- DHA05602784706
Company information
- Manufacturer
- BIOSENSE WEBSTER, INC.
- Manufacturer Country
- United States
- Authorized Representative
- JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
Product details
- Product Type (Level 1)
- E Cardiovascular devices
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 11, 2015
- Expiry Date
- Nov 11, 2020
- Cancellation Date
- Nov 22, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for “Biosense Webster” nMARQ Multi-Channel RF Generator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 9dad7430347f3bb995cba3b9b87286c7 and manufactured by BIOSENSE WEBSTER, INC.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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