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“IBI” Swissbone Bone Substitute - Taiwan Registration 91cc5c6b2d7cfb0c3d473d6ae0eb57f2

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..

This page provides complete technical specifications, regulatory compliance details. 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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91cc5c6b2d7cfb0c3d473d6ae0eb57f2
Registration Details
Taiwan FDA Registration: 91cc5c6b2d7cfb0c3d473d6ae0eb57f2
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Device Details

“IBI” Swissbone Bone Substitute
TW: “艾必瑞士”骨替代物
Risk Class 2
MD

Registration Details

91cc5c6b2d7cfb0c3d473d6ae0eb57f2

Ministry of Health Medical Device Import No. 036045

DHA05603604500

Company Information

Switzerland

Product Details

Details are as detailed as approved Chinese instructions

F Dentistry

F3930 Alveolar Restoration Materials

Imported from abroad

Dates and Status

Nov 16, 2022

Jul 07, 2027