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“DenFil N” Light-cured restorative nano hybrid composite resin - Taiwan Registration e333a2a58c862a12117cef147fd2f1ed

Access comprehensive regulatory information for “DenFil N” Light-cured restorative nano hybrid 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 e333a2a58c862a12117cef147fd2f1ed and manufactured by VERICOM CO., LTD.. The authorized representative in Taiwan is SUNDENT CORPORATION.

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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e333a2a58c862a12117cef147fd2f1ed
Registration Details
Taiwan FDA Registration: e333a2a58c862a12117cef147fd2f1ed
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Device Details

“DenFil N” Light-cured restorative nano hybrid composite resin
TW: “登飛奈米”光聚合複合樹脂
Risk Class 2
MD

Registration Details

e333a2a58c862a12117cef147fd2f1ed

Ministry of Health Medical Device Import No. 030968

DHA05603096802

Company Information

Korea, Republic of

Product Details

For details, it is Chinese approved copy of the imitation order

F Dental devices

F3690 Resin tusk wood

Imported from abroad

Dates and Status

Mar 15, 2018

Mar 15, 2028