Taiwan FDA registration 578c2f31ddcefc2a9561bb831c86c0f5

“IBI” SmartBone bone substitute

TW: “艾必亞”骨替代物
Taiwan flagTaiwan·Risk Class 2·MD·Industrie Biomediche Insubri SA·Registered Jul 07, 2022 – Jul 07, 2027Active
Registration details
Analysis ID
578c2f31ddcefc2a9561bb831c86c0f5
License Form
Ministry of Health Medical Device Import No. 035703
Customs Code
DHA05603570304
Company information
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
Jul 07, 2022
Expiry Date
Jul 07, 2027
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About this record

Access comprehensive regulatory information for “IBI” SmartBone 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 578c2f31ddcefc2a9561bb831c86c0f5 and manufactured by Industrie Biomediche Insubri SA. The authorized representative in Taiwan is PORTLAND BIOTECHNICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Industrie Biomediche Insubri SA, and 1 recent registrations in the same category. 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.

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