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“TISS” GBR-Tent Screw - Taiwan Registration db03d8f50bc1caff8672873647e32516

Access comprehensive regulatory information for “TISS” GBR-Tent Screw in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number db03d8f50bc1caff8672873647e32516 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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db03d8f50bc1caff8672873647e32516
Registration Details
Taiwan FDA Registration: db03d8f50bc1caff8672873647e32516
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Device Details

“TISS” GBR-Tent Screw
TW: “皇亮生醫”牙科補骨支撐螺釘
Risk Class 2
MD

Registration Details

db03d8f50bc1caff8672873647e32516

Ministry of Health Medical Device Manufacturing No. 005882

Company Information

Taiwan, Province of China

Product Details

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

F Dental devices

F4880 Intraosseous fixing screws or metal wires

Produced in Taiwan, China

Dates and Status

Jul 04, 2017

Jul 04, 2027