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“Horien” Collagen Bone Graft Matrix - Taiwan Registration 256ec21a672989c37e8b2957dccb5c70

Access comprehensive regulatory information for “Horien” Collagen Bone Graft Matrix in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 256ec21a672989c37e8b2957dccb5c70 and manufactured by HORIEN BIOCHEMICAL TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is HORIEN BIOCHEMICAL TECHNOLOGY 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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256ec21a672989c37e8b2957dccb5c70
Registration Details
Taiwan FDA Registration: 256ec21a672989c37e8b2957dccb5c70
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Device Details

“Horien” Collagen Bone Graft Matrix
TW: “海昌”膠原蛋白骨填料
Risk Class 2
MD

Registration Details

256ec21a672989c37e8b2957dccb5c70

Ministry of Health Medical Device Manufacturing No. 005064

Company Information

Taiwan, Province of China

Product Details

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

F Dental devices

F3930 Tricalcium phosphate for alveolar bone restoration

Produced in Taiwan, China

Dates and Status

Sep 01, 2015

Sep 01, 2025