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“Horien” Extracellular Membrane - Taiwan Registration fd727c920c29de7587240c0e36edd11f

Access comprehensive regulatory information for “Horien” Extracellular Membrane in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fd727c920c29de7587240c0e36edd11f 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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fd727c920c29de7587240c0e36edd11f
Registration Details
Taiwan FDA Registration: fd727c920c29de7587240c0e36edd11f
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Device Details

“Horien” Extracellular Membrane
TW: “海昌”膠原再生薄膜
Risk Class 2
MD

Registration Details

fd727c920c29de7587240c0e36edd11f

Ministry of Health Medical Device Manufacturing No. 005701

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

Feb 16, 2017

Feb 16, 2027