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“HONHI” Gutta Percha (Non-Sterile) - Taiwan Registration f45e3497bb4eadae6db5298360bff27c

Access comprehensive regulatory information for “HONHI” Gutta Percha (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 f45e3497bb4eadae6db5298360bff27c and manufactured by PEARL DENT CO., LTD. The authorized representative in Taiwan is HONHI MEDICAL 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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f45e3497bb4eadae6db5298360bff27c
Registration Details
Taiwan FDA Registration: f45e3497bb4eadae6db5298360bff27c
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Device Details

“HONHI” Gutta Percha (Non-Sterile)
TW: “鴻海”馬來膠 (未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

f45e3497bb4eadae6db5298360bff27c

Ministry of Health Medical Device Import No. 014835

DHA09401483501

Company Information

Viet Nam

Product Details

F Dental devices

F3850 Male-Glue

Imported from abroad

Dates and Status

Jan 09, 2015

Jan 09, 2020

Jul 15, 2022

Cancellation Information

Logged out

未展延而逾期者