Taiwan FDA registration 778bad1a84e7fff45b06e96e3fb1d5fb
OsteoSelect PLUS DBM Putty
TW: 歐特選加去礦化補骨物
Taiwan·Risk Class 2·MD·Xtant Medical Holdings, Inc.·Registered Jul 23, 2018 – Jul 23, 2028ActiveRegistration details
- Analysis ID
- 778bad1a84e7fff45b06e96e3fb1d5fb
- License Form
- Ministry of Health Medical Device Import No. 031355
- Customs Code
- DHA05603135500
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
- Jul 23, 2018
- Expiry Date
- Jul 23, 2028
About this record
Access comprehensive regulatory information for OsteoSelect PLUS 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 778bad1a84e7fff45b06e96e3fb1d5fb and manufactured by Xtant Medical Holdings, Inc.. The authorized representative in Taiwan is ALSTRONG SCIENTIFIC INTERNATIONAL LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices