Taiwan FDA registration 434305213e8b8ab15ff01da57e17a2ea
"Bone Lux" absorbs regenerative membranes
TW: “骨力士”可吸收再生膜
Taiwan·Risk Class 2·BOTISS BIOMATERIALS GMBH·Registered Feb 23, 2020 – Feb 23, 2030ActiveRegistration details
- Analysis ID
- 434305213e8b8ab15ff01da57e17a2ea
- Customs Code
- DHA05603335602
Company information
- Manufacturer
- BOTISS BIOMATERIALS GMBH
- Manufacturer Country
- Germany
- 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.3930 Alveolar repair materials
- Import Information
- import
Dates and status
- Registration Date
- Feb 23, 2020
- Expiry Date
- Feb 23, 2030
About this record
Access comprehensive regulatory information for "Bone Lux" absorbs regenerative membranes in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 434305213e8b8ab15ff01da57e17a2ea and manufactured by BOTISS BIOMATERIALS GMBH. The authorized representative in Taiwan is Straumann Group (Taiwan) Co. Ltd..
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