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“PULPDENT” ACTIVA Bio ACTIVE-RESTORATIVE - Taiwan Registration 4ac6ec4a16a795d368aa8de3144079f4

Access comprehensive regulatory information for “PULPDENT” ACTIVA Bio ACTIVE-RESTORATIVE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4ac6ec4a16a795d368aa8de3144079f4 and manufactured by PULPDENT CORPORATION. The authorized representative in Taiwan is FRANKFURT TECHNOLOGY CO., LTD..

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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4ac6ec4a16a795d368aa8de3144079f4
Registration Details
Taiwan FDA Registration: 4ac6ec4a16a795d368aa8de3144079f4
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Device Details

“PULPDENT” ACTIVA Bio ACTIVE-RESTORATIVE
TW: “波普登”玻璃離子補牙材
Risk Class 2
MD

Registration Details

4ac6ec4a16a795d368aa8de3144079f4

Ministry of Health Medical Device Import No. 032532

DHA05603253201

Company Information

United States

Product Details

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

F Dental devices

F3275 Dental cement (Sminting)

Imported from abroad

Dates and Status

May 01, 2019

May 01, 2024