Taiwan FDA registration eb89549523cebffe755eac831a4e2e2f
"Staulman" pure titanosin bone explant (bone height)
TW: “史得勞曼”純鈦洛新骨內植體(骨高度)
Taiwan·Risk Class 3·Straumann Villeret SA;; Institut Straumann AG·Registered Jan 06, 2017 – Jan 06, 2027ActiveRegistration details
- Analysis ID
- eb89549523cebffe755eac831a4e2e2f
- Customs Code
- DHA05602925007
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
- Jan 06, 2017
- Expiry Date
- Jan 06, 2027
About this record
Access comprehensive regulatory information for "Staulman" pure titanosin bone explant (bone height) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number eb89549523cebffe755eac831a4e2e2f and manufactured by Straumann Villeret SA;; Institut Straumann AG. The authorized representative in Taiwan is Straumann Group (Taiwan) Co. Ltd..
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