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"DENTSPLY Professional" Dental hand instrument (Non-Sterile) - Taiwan Registration f876175f4f9c0222db99e4f06df1ea18

Access comprehensive regulatory information for "DENTSPLY Professional" Dental hand 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 f876175f4f9c0222db99e4f06df1ea18 and manufactured by DENTSPLY PROFESSIONAL. The authorized representative in Taiwan is Taiwan Branch of American Denspie 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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f876175f4f9c0222db99e4f06df1ea18
Registration Details
Taiwan FDA Registration: f876175f4f9c0222db99e4f06df1ea18
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Device Details

"DENTSPLY Professional" Dental hand instrument (Non-Sterile)
TW: "็™ปๅฃซๆดพ" ็‰™็ง‘ๆ‰‹็”จๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

f876175f4f9c0222db99e4f06df1ea18

Ministry of Health Medical Device Import No. 014162

DHA09401416202

Company Information

United States

Product Details

F Dental devices

F4565 Hand instruments for dental use

Imported from abroad

Dates and Status

May 23, 2014

May 23, 2019

Jul 15, 2022

Cancellation Information

Logged out

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