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“Lancer”Dental hand instrument (Non-Sterile) - Taiwan Registration f27dcc6e4b555903b388eb31c053c2cd

Access comprehensive regulatory information for “Lancer”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 f27dcc6e4b555903b388eb31c053c2cd and manufactured by LANCER ORTHODONTICS, INC.. The authorized representative in Taiwan is A & J BROS. TRADING 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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f27dcc6e4b555903b388eb31c053c2cd
Registration Details
Taiwan FDA Registration: f27dcc6e4b555903b388eb31c053c2cd
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Device Details

“Lancer”Dental hand instrument (Non-Sterile)
TW: “藍偲”牙科手用器械 (未滅菌)
Risk Class 1
MD

Registration Details

f27dcc6e4b555903b388eb31c053c2cd

Ministry of Health Medical Device Import No. 022297

DHA09402229705

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

Feb 04, 2021

Feb 04, 2026