Taiwan FDA registration e2c15f375856c0fd910c27433397c278
"Straumann" pure titanium neoosse in-bone explant (tissue height)
TW: “史得勞曼”純鈦洛新骨內植體(組織高度)
Taiwan·Risk Class 3·Straumann Villeret SA;; Institut Straumann AG·Registered Jan 13, 2017 – Jan 13, 2027ActiveRegistration details
- Analysis ID
- e2c15f375856c0fd910c27433397c278
- Customs Code
- DHA05602934202
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 13, 2017
- Expiry Date
- Jan 13, 2027
About this record
Access comprehensive regulatory information for "Straumann" pure titanium neoosse in-bone explant (tissue height) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number e2c15f375856c0fd910c27433397c278 and manufactured by Straumann Villeret SA;; Institut Straumann AG. The authorized representative in Taiwan is Straumann Group (Taiwan) Co. Ltd..
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