Taiwan FDA registration 17c7285530ce5f3a32e94efdc14407b3
“Straumann” XenoGraft
TW: “士卓曼”塞若骨補骨用骨粉
Taiwan·Risk Class 2·MD·NIBEC Co., Ltd·Registered Mar 04, 2021 – Nov 11, 2025ExpiredRegistration details
- Analysis ID
- 17c7285530ce5f3a32e94efdc14407b3
- License Form
- Ministry of Health Medical Device Import No. 034300
- Customs Code
- DHA05603430003
Company information
- Manufacturer
- NIBEC Co., Ltd
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Straumann Group (Taiwan) Co. Ltd.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3930 Alveolar Restoration Materials
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 04, 2021
- Expiry Date
- Nov 11, 2025
About this record
Access comprehensive regulatory information for “Straumann” XenoGraft in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 17c7285530ce5f3a32e94efdc14407b3 and manufactured by NIBEC Co., Ltd. The authorized representative in Taiwan is Straumann Group (Taiwan) Co. Ltd..
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