Taiwan FDA registration 91cc5c6b2d7cfb0c3d473d6ae0eb57f2
“IBI” Swissbone Bone Substitute
TW: “艾必瑞士”骨替代物
Taiwan·Risk Class 2·MD·Industrie Biomediche Insubri SA·Registered Nov 16, 2022 – Jul 07, 2027ActiveRegistration details
- Analysis ID
- 91cc5c6b2d7cfb0c3d473d6ae0eb57f2
- License Form
- Ministry of Health Medical Device Import No. 036045
- Customs Code
- DHA05603604500
Company information
- Manufacturer
- Industrie Biomediche Insubri SA
- Manufacturer Country
- Switzerland
- Authorized Representative
- PORTLAND BIOTECHNICAL CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F3930 Alveolar Restoration Materials
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 16, 2022
- Expiry Date
- Jul 07, 2027
About this record
Access comprehensive regulatory information for “IBI” Swissbone Bone Substitute in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 91cc5c6b2d7cfb0c3d473d6ae0eb57f2 and manufactured by Industrie Biomediche Insubri SA. The authorized representative in Taiwan is PORTLAND BIOTECHNICAL CO., LTD..
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