Taiwan FDA registration 25bca7265b4838278799ef343962ae80
"Straumann" pure titanonew bone explant (bone height tapered)
TW: “史得勞曼”純鈦洛新骨內植體(骨高度錐形)
Taiwan·Risk Class 3·Straumann Villeret SA;; Institut Straumann AG·Registered Sep 22, 2015 – Sep 22, 2025ExpiredRegistration details
- Analysis ID
- 25bca7265b4838278799ef343962ae80
- Customs Code
- DHA05602779401
Company information
- Manufacturer
- Straumann Villeret SA;; Institut Straumann AG
- Manufacturer Country
- Switzerland
- 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 Dentistry
- Product Type (Level 2)
- F.3640 Bone Implants
- Import Information
- import
Dates and status
- Registration Date
- Sep 22, 2015
- Expiry Date
- Sep 22, 2025
About this record
Access comprehensive regulatory information for "Straumann" pure titanonew bone explant (bone height tapered) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 25bca7265b4838278799ef343962ae80 and manufactured by Straumann Villeret SA;; Institut Straumann AG. The authorized representative in Taiwan is Straumann Group (Taiwan) Co. 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