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“SDI” Luna Nano-Hybrid Composite Restorative Material - Taiwan Registration 212bb5e5d2f37670c343a90037bbc4e0

Access comprehensive regulatory information for “SDI” Luna Nano-Hybrid Composite 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 212bb5e5d2f37670c343a90037bbc4e0 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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212bb5e5d2f37670c343a90037bbc4e0
Registration Details
Taiwan FDA Registration: 212bb5e5d2f37670c343a90037bbc4e0
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Device Details

“SDI” Luna Nano-Hybrid Composite Restorative Material
TW: “斯蒂爾”路納複合型補牙材
Risk Class 2
MD

Registration Details

212bb5e5d2f37670c343a90037bbc4e0

Ministry of Health Medical Device Import No. 035062

DHA05603506205

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

Nov 18, 2021

Nov 18, 2026