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"DyanFlex" Dental Hand Instrument (Non-Sterile) - Taiwan Registration f82bbf42313271c2ffdadc58de65fe68

Access comprehensive regulatory information for "DyanFlex" 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 f82bbf42313271c2ffdadc58de65fe68 and manufactured by DyanFlex. The authorized representative in Taiwan is PULLIER 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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f82bbf42313271c2ffdadc58de65fe68
Registration Details
Taiwan FDA Registration: f82bbf42313271c2ffdadc58de65fe68
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Device Details

"DyanFlex" Dental Hand Instrument (Non-Sterile)
TW: "้ป›ๅจœๅฆƒ"็‰™็ง‘ๆ‰‹็”จๅ™จๆขฐ(ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

f82bbf42313271c2ffdadc58de65fe68

Ministry of Health Medical Device Import No. 015320

DHA09401532009

Company Information

United States

Product Details

F Dental devices

F4565 Hand instruments for dental use

Imported from abroad

Dates and Status

Jun 09, 2015

Jun 09, 2020

Aug 05, 2022

Cancellation Information

Logged out

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