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"Perfection" Dental Hand Instrument (Non-Sterile) - Taiwan Registration 235d95381bfc9bed77e0c0a8ace46efa

Access comprehensive regulatory information for "Perfection" 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 235d95381bfc9bed77e0c0a8ace46efa and manufactured by PERFECTION PLUS LTD.. The authorized representative in Taiwan is SMART LIFE INTERNATIONAL 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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235d95381bfc9bed77e0c0a8ace46efa
Registration Details
Taiwan FDA Registration: 235d95381bfc9bed77e0c0a8ace46efa
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Device Details

"Perfection" Dental Hand Instrument (Non-Sterile)
TW: "ๅš้ฃ›ๆ–ฐ" ็‰™็ง‘ๆ‰‹็”จๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

235d95381bfc9bed77e0c0a8ace46efa

Ministry of Health Medical Device Import No. 018244

DHA09401824408

Company Information

United Kingdom

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

Aug 29, 2017

Aug 29, 2022