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3M ESPE Filtek Bulk Fill Posterior Restorative - Taiwan Registration 98fbc214e97e70dc79d4dc18fb4ba9e2

Access comprehensive regulatory information for 3M ESPE Filtek Bulk Fill Posterior Restorative in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 98fbc214e97e70dc79d4dc18fb4ba9e2 and manufactured by 3M ESPE DENTAL PRODUCTS. The authorized representative in Taiwan is Taiwan Minnesota Mining Manufacturing 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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98fbc214e97e70dc79d4dc18fb4ba9e2
Registration Details
Taiwan FDA Registration: 98fbc214e97e70dc79d4dc18fb4ba9e2
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Device Details

3M ESPE Filtek Bulk Fill Posterior Restorative
TW: 3M่ฒ็‰นๆณขๅ…‹้ฝ’้ซ”ๅกซๅ……ๅพŒ็‰™ๅพฉๅฝขๆๆ–™
Risk Class 2
MD

Registration Details

98fbc214e97e70dc79d4dc18fb4ba9e2

Ministry of Health Medical Device Import No. 027378

DHA05602737800

Company Information

United States

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

May 04, 2015

May 04, 2025