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“Dreve” Fresh Impression Materials - Taiwan Registration 1261ada2c8c62add3471d6e675f86dc2

Access comprehensive regulatory information for “Dreve” Fresh Impression Materials in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1261ada2c8c62add3471d6e675f86dc2 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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1261ada2c8c62add3471d6e675f86dc2
Registration Details
Taiwan FDA Registration: 1261ada2c8c62add3471d6e675f86dc2
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Device Details

“Dreve” Fresh Impression Materials
TW: “德瑞芙”飛喜加成型印模材料
Risk Class 2
MD

Registration Details

1261ada2c8c62add3471d6e675f86dc2

Ministry of Health Medical Device Import No. 030553

DHA05603055302

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

Nov 15, 2017

Nov 15, 2022