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“SDI” Aura eASY Ultra Universal Restorative Material - Taiwan Registration 49a314cb7e2f8e353b46ab82e5ddae1f

Access comprehensive regulatory information for “SDI” Aura eASY Ultra 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 49a314cb7e2f8e353b46ab82e5ddae1f 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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49a314cb7e2f8e353b46ab82e5ddae1f
Registration Details
Taiwan FDA Registration: 49a314cb7e2f8e353b46ab82e5ddae1f
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Device Details

“SDI” Aura eASY Ultra Universal Restorative Material
TW: “斯蒂爾”歐拉易通用型樹脂補牙材
Risk Class 2
MD

Registration Details

49a314cb7e2f8e353b46ab82e5ddae1f

Ministry of Health Medical Device Import No. 035084

DHA05603508402

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 09, 2021

Dec 09, 2026