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“DENTAMERICA” Premier Diamond Instrument (Non-Sterile) - Taiwan Registration aa80ec71f0cf697a188487aee834c161

Access comprehensive regulatory information for “DENTAMERICA” Premier Diamond Instrument (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number aa80ec71f0cf697a188487aee834c161 and manufactured by Qiqi Technology Co., Ltd. Xizhi factory. The authorized representative in Taiwan is Qiqi Technology Co., Ltd. Xizhi factory.

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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aa80ec71f0cf697a188487aee834c161
Registration Details
Taiwan FDA Registration: aa80ec71f0cf697a188487aee834c161
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Device Details

“DENTAMERICA” Premier Diamond Instrument (Non-Sterile)
TW: “登特美”牙科用鑽石器械 (未滅菌)
Risk Class 1
MD

Registration Details

aa80ec71f0cf697a188487aee834c161

Ministry of Health Medical Device Manufacturing No. 007909

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of dental diamond instruments (F.4535) under the Measures for the Administration of Medical Equipment.

F Dental devices

F4535 Dental Diamond Instruments

Produced in Taiwan, China

Dates and Status

Aug 21, 2019

Aug 21, 2024