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"Dretta" root canal center column nail (unsterilized) - Taiwan Registration 09e6e3cb3a46bcee6ebe87364d52c806

Access comprehensive regulatory information for "Dretta" root canal center column nail (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 09e6e3cb3a46bcee6ebe87364d52c806 and manufactured by DIRECT AB. The authorized representative in Taiwan is SHIN YEAN 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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09e6e3cb3a46bcee6ebe87364d52c806
Registration Details
Taiwan FDA Registration: 09e6e3cb3a46bcee6ebe87364d52c806
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Device Details

"Dretta" root canal center column nail (unsterilized)
TW: "ๅพท็‘žๅก”" ๆ น็ฎกไธญๅฟƒๆŸฑ้‡˜ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

09e6e3cb3a46bcee6ebe87364d52c806

DHA04400971300

Company Information

Sweden

Product Details

It is limited to the first-level identification scope of the "Root Canal Center Pillar (F.3810)" of the Classification and Grading Management Measures for Medical Devices.

F Dentistry

F.3810 Root canal center post

import

Dates and Status

Dec 20, 2010

Dec 20, 2025