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“BesTISS” Dental Implant - Taiwan Registration dfe706cee0df2e157f27aa49d7e8b737

Access comprehensive regulatory information for “BesTISS” Dental Implant in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number dfe706cee0df2e157f27aa49d7e8b737 and manufactured by HUANG LIANG BIOMEDICAL TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is HUANG LIANG BIOMEDICAL 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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dfe706cee0df2e157f27aa49d7e8b737
Registration Details
Taiwan FDA Registration: dfe706cee0df2e157f27aa49d7e8b737
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Device Details

“BesTISS” Dental Implant
TW: “皇亮生醫”人工牙根
Risk Class 3
MD

Registration Details

dfe706cee0df2e157f27aa49d7e8b737

Ministry of Health Medical Device Manufacturing No. 005472

Company Information

Taiwan, Province of China

Product Details

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

F Dental devices

F3640 Bone explants

Produced in Taiwan, China

Dates and Status

Nov 11, 2016

Nov 11, 2026