Taiwan FDA registration 775affb449221ae084bab965e1bba7ba
Biosonic bone cutter
TW: 必適通超音波骨切割器
Taiwan·Risk Class 2·SATELEC, A COMPANY OF ACTEON GROUP·Registered May 16, 2013 – May 16, 2018CancelledRegistration details
- Analysis ID
- 775affb449221ae084bab965e1bba7ba
- Customs Code
- DHA00602503006
Company information
- Manufacturer
- SATELEC, A COMPANY OF ACTEON GROUP
- Manufacturer Country
- France
- Authorized Representative
- FABRO INTERNATIONAL CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.4120 Bone cutters and accessories thereof
- Import Information
- import
Dates and status
- Registration Date
- May 16, 2013
- Expiry Date
- May 16, 2018
- 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 Biosonic bone cutter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 775affb449221ae084bab965e1bba7ba and manufactured by SATELEC, A COMPANY OF ACTEON GROUP. The authorized representative in Taiwan is FABRO INTERNATIONAL CO., LTD..
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