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“INTRA-LOCK” ReOss Synthetic Biomaterial - Taiwan Registration b461d1463ef4d569672e43cc563b06ec

Access comprehensive regulatory information for “INTRA-LOCK” ReOss Synthetic Biomaterial in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b461d1463ef4d569672e43cc563b06ec and manufactured by INTRA-LOCK INTERNATIONAL, INC.. The authorized representative in Taiwan is HONG YANG BIOTECHNOLOGY 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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b461d1463ef4d569672e43cc563b06ec
Registration Details
Taiwan FDA Registration: b461d1463ef4d569672e43cc563b06ec
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Device Details

“INTRA-LOCK” ReOss Synthetic Biomaterial
TW: “英德樂可”里奧斯合成骨粉
Risk Class 2
MD

Registration Details

b461d1463ef4d569672e43cc563b06ec

Ministry of Health Medical Device Import No. 026322

DHA05602632204

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

F Dental devices

F3930 Tricalcium phosphate for alveolar bone restoration

Imported from abroad

Dates and Status

Jul 02, 2014

Jul 02, 2024