Taiwan FDA registration 47667a41a90a199159d19cb9bae7166c
"Bischen" plaster removal device (unsterilized)
TW: “必史恩” 石膏拆除器械(未滅菌)
Taiwan·Risk Class 1·BSN MEDICAL INC.·Registered Feb 13, 2012 – Feb 13, 2022CancelledRegistration details
- Analysis ID
- 47667a41a90a199159d19cb9bae7166c
- Customs Code
- DHA04401136709
Company information
- Manufacturer
- BSN MEDICAL INC.
- Manufacturer Country
- United States
- Authorized Representative
- SUNSHINE INSTRUMENT LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Gypsum Removal Devices (N.5960)".
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.5960 石膏拆除器械
- Import Information
- import
Dates and status
- Registration Date
- Feb 13, 2012
- Expiry Date
- Feb 13, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Bischen" plaster removal device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 47667a41a90a199159d19cb9bae7166c and manufactured by BSN MEDICAL INC.. The authorized representative in Taiwan is SUNSHINE INSTRUMENT LTD..
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