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"Huangliang Biodoctor" mesh fixing system - Taiwan Registration ad09ad46218ecf953eba431bfb9f5263

Access comprehensive regulatory information for "Huangliang Biodoctor" mesh fixing system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ad09ad46218ecf953eba431bfb9f5263 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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ad09ad46218ecf953eba431bfb9f5263
Registration Details
Taiwan FDA Registration: ad09ad46218ecf953eba431bfb9f5263
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Device Details

"Huangliang Biodoctor" mesh fixing system
TW: โ€œ็š‡ไบฎ็”Ÿ้†ซโ€็ถฒ็‰‡ๅ›บๅฎš็ณป็ตฑ
Risk Class 2

Registration Details

ad09ad46218ecf953eba431bfb9f5263

Company Information

Taiwan, Province of China

Product Details

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

F Dentistry

F.4760 ้ชจๆฟ;; F.4880 ้ชจๅ…งๅ›บๅฎš่žบ้‡˜ๆˆ–้‡‘ๅฑฌ็ทš

Domestic

Dates and Status

Nov 08, 2017

Nov 08, 2027