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“SDI” Wave Flowable Releasing Composite - Taiwan Registration 96fa5a76365732332701dc84aa652e9a

Access comprehensive regulatory information for “SDI” Wave Flowable Releasing Composite in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 96fa5a76365732332701dc84aa652e9a 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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96fa5a76365732332701dc84aa652e9a
Registration Details
Taiwan FDA Registration: 96fa5a76365732332701dc84aa652e9a
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Device Details

“SDI” Wave Flowable Releasing Composite
TW: “斯蒂爾”維夫流動性樹脂補牙材
Risk Class 2
MD

Registration Details

96fa5a76365732332701dc84aa652e9a

Ministry of Health Medical Device Import No. 034979

DHA05603497901

Company Information

Australia

Product Details

Details are as detailed as approved Chinese instructions

F Dental devices

F3690 Resin tusk wood

Imported from abroad

Dates and Status

Oct 22, 2021

Oct 22, 2026