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"OVERFIBERS" Root canal post (Non-Sterile) - Taiwan Registration e16392daa271309fa7d02ca4a121be3f

Access comprehensive regulatory information for "OVERFIBERS" Root canal post (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 e16392daa271309fa7d02ca4a121be3f and manufactured by OVERFIBERS S.R.L.. The authorized representative in Taiwan is EUROTIDE TECHNOLOGY 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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e16392daa271309fa7d02ca4a121be3f
Registration Details
Taiwan FDA Registration: e16392daa271309fa7d02ca4a121be3f
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Device Details

"OVERFIBERS" Root canal post (Non-Sterile)
TW: "ๆญๅšๅฃซ" ๆ น็ฎกไธญๅฟƒๆŸฑ้‡˜ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

e16392daa271309fa7d02ca4a121be3f

Ministry of Health Medical Device Import No. 015667

DHA09401566708

Company Information

Italy

Product Details

F Dental devices

F3810 tube center column nail

Imported from abroad

Dates and Status

Sep 14, 2015

Sep 14, 2020

Jul 15, 2022

Cancellation Information

Logged out

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