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"DiaDent" Dental Hand Instrument (Non-Sterile) - Taiwan Registration efffd0250e619715d4caaf69388e35fd

Access comprehensive regulatory information for "DiaDent" 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 efffd0250e619715d4caaf69388e35fd and manufactured by DiaDent Group International. The authorized representative in Taiwan is ASIANTOP ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including DIADENT GROUP INTERNATIONAL, DIADENT GROUP INTERNATIONAL (KOREA & INTERNATIONAL), and 2 recent registrations in the same category. 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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Registration Details
Taiwan FDA Registration: efffd0250e619715d4caaf69388e35fd
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Device Details

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

Registration Details

efffd0250e619715d4caaf69388e35fd

Ministry of Health Medical Device Import No. 015627

DHA09401562709

Company Information

Korea, Republic of

Product Details

F Dental devices

F4565 Hand instruments for dental use

Imported from abroad

Dates and Status

Sep 01, 2015

Sep 01, 2020

Jul 15, 2022

Cancellation Information

Logged out

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