Taiwan FDA registration abf37adc70dec7c85f3b972092cdd4e8
“Xtant”OsteoSelect DBM Putty
TW: “艾斯坦”歐特選去礦化補骨物
Taiwan·Risk Class 2·MD·Xtant Medical Holdings, Inc.·Registered Feb 01, 2016 – Feb 01, 2026ExpiredRegistration details
- Analysis ID
- abf37adc70dec7c85f3b972092cdd4e8
- License Form
- Ministry of Health Medical Device Import No. 028178
- Customs Code
- DHA05602817807
Company information
- Manufacturer
- Xtant Medical Holdings, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- ALSTRONG SCIENTIFIC INTERNATIONAL LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3045 Resorbed calcium salt bone cavity filling device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 01, 2016
- Expiry Date
- Feb 01, 2026
About this record
Access comprehensive regulatory information for “Xtant”OsteoSelect DBM Putty in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number abf37adc70dec7c85f3b972092cdd4e8 and manufactured by Xtant Medical Holdings, Inc.. The authorized representative in Taiwan is ALSTRONG SCIENTIFIC INTERNATIONAL LTD..
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