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“TELLUS” Anchorage Screws - Taiwan Registration d7296227df4468bccba7c3d02aa13151

Access comprehensive regulatory information for “TELLUS” Anchorage Screws in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number d7296227df4468bccba7c3d02aa13151 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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d7296227df4468bccba7c3d02aa13151
Registration Details
Taiwan FDA Registration: d7296227df4468bccba7c3d02aa13151
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Device Details

“TELLUS” Anchorage Screws
TW: “鈦樂”牙科矯正釘
Risk Class 3
MD

Registration Details

d7296227df4468bccba7c3d02aa13151

Ministry of Health Medical Device Manufacturing No. 006009

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

Dec 05, 2017

Mar 23, 2027