Taiwan FDA registration aaa8782324ec6ed287a5ae173317aa16
“XiVE” S Plus Implant System
TW: “賽芙”牙科植體。
Taiwan·Risk Class 3·MD·DENTSPLY IMPLANTS MANUFACTURING GMBH·Registered Jun 29, 2010 – Jun 29, 2025ExpiredRegistration details
- Analysis ID
- aaa8782324ec6ed287a5ae173317aa16
- License Form
- Department of Health Medical Device Import No. 021171
- Customs Code
- DHA00602117104
Company information
- Manufacturer
- DENTSPLY IMPLANTS MANUFACTURING GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- DENTSPLY SIRONA INC., TAIWAN BRANCH (U.S.A.)
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)
- F3640 Bone explants
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 29, 2010
- Expiry Date
- Jun 29, 2025
About this record
Access comprehensive regulatory information for “XiVE” S Plus Implant System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number aaa8782324ec6ed287a5ae173317aa16 and manufactured by DENTSPLY IMPLANTS MANUFACTURING GMBH. The authorized representative in Taiwan is DENTSPLY SIRONA INC., TAIWAN BRANCH (U.S.A.).
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