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“Dreve” Stonebite Bite Registration Material - Taiwan Registration 9c4deae1f266e92c0c2cbf48bbb74606

Access comprehensive regulatory information for “Dreve” Stonebite Bite Registration Material in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9c4deae1f266e92c0c2cbf48bbb74606 and manufactured by DREVE DENTAMID GMBH. The authorized representative in Taiwan is MNM BIOTECHNOLOGY 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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9c4deae1f266e92c0c2cbf48bbb74606
Registration Details
Taiwan FDA Registration: 9c4deae1f266e92c0c2cbf48bbb74606
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Device Details

“Dreve” Stonebite Bite Registration Material
TW: “德瑞芙”始動咬合記錄材
Risk Class 2
MD

Registration Details

9c4deae1f266e92c0c2cbf48bbb74606

Ministry of Health Medical Device Import No. 031269

DHA05603126907

Company Information

Germany

Product Details

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

F Dental devices

F3660 impression material

Imported from abroad

Dates and Status

Jun 29, 2018

Jun 29, 2028