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“Keystone” Dental Hand Instrument (Non-Sterile) - Taiwan Registration a4da8281749a585957d51118dab6ee75

Access comprehensive regulatory information for “Keystone” 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 a4da8281749a585957d51118dab6ee75 and manufactured by KEYSTONE DENTAL, INC.. The authorized representative in Taiwan is HUNG KUO MEDICAL INSTRUMENT 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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a4da8281749a585957d51118dab6ee75
Registration Details
Taiwan FDA Registration: a4da8281749a585957d51118dab6ee75
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Device Details

“Keystone” Dental Hand Instrument (Non-Sterile)
TW: “金石”牙科手用器械 (未滅菌) 
Risk Class 1
MD

Registration Details

a4da8281749a585957d51118dab6ee75

Ministry of Health Medical Device Import No. 014177

DHA09401417702

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Dental Hand Instruments (F.4565)".

F Dental devices

F4565 Hand instruments for dental use

Imported from abroad

Dates and Status

May 28, 2014

May 28, 2024