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“TELLUS” Implant-Abutment System - Taiwan Registration a0b8f14cd83215b9948bbd631034ffa9

Access comprehensive regulatory information for “TELLUS” Implant-Abutment System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a0b8f14cd83215b9948bbd631034ffa9 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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a0b8f14cd83215b9948bbd631034ffa9
Registration Details
Taiwan FDA Registration: a0b8f14cd83215b9948bbd631034ffa9
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Device Details

“TELLUS” Implant-Abutment System
TW: "鈦樂" 支台體系統
Risk Class 2
MD

Registration Details

a0b8f14cd83215b9948bbd631034ffa9

Ministry of Health Medical Device Manufacturing No. 005251

Company Information

Taiwan, Province of China

Product Details

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

F Dental devices

F3630 Dental bridges for bone explants

Produced in Taiwan, China

Dates and Status

Dec 24, 2015

May 01, 2025