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"SPIDENT" Gutta Percha (Non-Sterile) - Taiwan Registration 323406df01d7827ae0bc08eb3f90133e

Access comprehensive regulatory information for "SPIDENT" Gutta Percha (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 323406df01d7827ae0bc08eb3f90133e and manufactured by SPIDENT CO., LTD.. The authorized representative in Taiwan is THONG TING TRADING COMPANY 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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323406df01d7827ae0bc08eb3f90133e
Registration Details
Taiwan FDA Registration: 323406df01d7827ae0bc08eb3f90133e
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Device Details

"SPIDENT" Gutta Percha (Non-Sterile)
TW: "ๅฒ็™พ็™ป" ้ฆฌไพ†่†  (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

323406df01d7827ae0bc08eb3f90133e

Ministry of Health Medical Device Import No. 015365

DHA09401536505

Company Information

Korea, Republic of

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Malay Rubber (F.3850)".

F Dental devices

F3850 Male-Glue

Imported from abroad

Dates and Status

Jun 18, 2015

Jun 18, 2025