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“SDI” Aura Bulk Fill Universal Restorative Material - Taiwan Registration 4c50013cb3936b805857a99f8465cccb

Access comprehensive regulatory information for “SDI” Aura Bulk Fill Universal Restorative Material in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4c50013cb3936b805857a99f8465cccb and manufactured by SDI Ltd. The authorized representative in Taiwan is FOMED BIOTECH INC..

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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4c50013cb3936b805857a99f8465cccb
Registration Details
Taiwan FDA Registration: 4c50013cb3936b805857a99f8465cccb
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Device Details

“SDI” Aura Bulk Fill Universal Restorative Material
TW: “斯蒂爾”歐拉巴克通用型樹脂補牙材
Risk Class 2
MD

Registration Details

4c50013cb3936b805857a99f8465cccb

Ministry of Health Medical Device Import No. 035095

DHA05603509507

Company Information

Australia

Product Details

Details are as detailed as approved Chinese instructions

F Dentistry

F3690 Resin tusk wood

Imported from abroad

Dates and Status

Dec 16, 2021

Dec 16, 2026