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ARNEL Dental hand Instruments (Non-Sterile) - Taiwan Registration f409cd17bb77bb453064f0d81b858ffd

Access comprehensive regulatory information for ARNEL Dental hand Instruments (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 f409cd17bb77bb453064f0d81b858ffd and manufactured by ARNEL, INC.. The authorized representative in Taiwan is SUN-BRIGHT DENTAL PRODUCT 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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f409cd17bb77bb453064f0d81b858ffd
Registration Details
Taiwan FDA Registration: f409cd17bb77bb453064f0d81b858ffd
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Device Details

ARNEL Dental hand Instruments (Non-Sterile)
TW: ๅฎ‰่ถ็‰™็ง‘ๆ‰‹็”จๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

f409cd17bb77bb453064f0d81b858ffd

Ministry of Health Medical Device Import No. 022247

DHA09402224703

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

Jan 14, 2021

Jan 14, 2026