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“B&E” Light-cured Composite Resin - Taiwan Registration eef68c220e1612580d4d9ecd12d2b842

Access comprehensive regulatory information for “B&E” Light-cured Composite Resin in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number eef68c220e1612580d4d9ecd12d2b842 and manufactured by B&E KOREA CO., LTD. The authorized representative in Taiwan is YOUNG SUN DEVELOP CO..

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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eef68c220e1612580d4d9ecd12d2b842
Registration Details
Taiwan FDA Registration: eef68c220e1612580d4d9ecd12d2b842
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Device Details

“B&E” Light-cured Composite Resin
TW: “賓益”樹脂牙材
Risk Class 2
MD

Registration Details

eef68c220e1612580d4d9ecd12d2b842

Ministry of Health Medical Device Import No. 034798

DHA05603479800

Company Information

Korea, Republic of

Product Details

Details are as detailed as approved Chinese instructions

F Dental devices

F3690 Resin tusk wood

Imported from abroad

Dates and Status

Jul 31, 2021

Jul 31, 2026