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"DXM" Guttapercha Obturation Device (Non-sterile) - Taiwan Registration 6fc91789f9c8229f5c6d9f3107ed624a

Access comprehensive regulatory information for "DXM" Guttapercha Obturation Device (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 6fc91789f9c8229f5c6d9f3107ed624a and manufactured by DXM CO., LTD.. The authorized representative in Taiwan is HONG HOW ENTERPRISE CO..

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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6fc91789f9c8229f5c6d9f3107ed624a
Registration Details
Taiwan FDA Registration: 6fc91789f9c8229f5c6d9f3107ed624a
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Device Details

"DXM" Guttapercha Obturation Device (Non-sterile)
TW: "ๅธๆ–ฏๆฉ"ๆ น็ฎก็†ฑๅ……ๅกซ่ฃ็ฝฎ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

6fc91789f9c8229f5c6d9f3107ed624a

Ministry of Health Medical Device Import No. 014440

DHA09401444001

Company Information

Korea, Republic of

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 19, 2014

Aug 19, 2024