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"Spiesden" root tube paper needle (unsterilized) - Taiwan Registration 349f3ae47b272bf2ee44a2f91cb95530

Access comprehensive regulatory information for "Spiesden" root tube paper needle (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 349f3ae47b272bf2ee44a2f91cb95530 and manufactured by SPIDENT CO. LTD.. The authorized representative in Taiwan is HON INTERNATIONAL 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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349f3ae47b272bf2ee44a2f91cb95530
Registration Details
Taiwan FDA Registration: 349f3ae47b272bf2ee44a2f91cb95530
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Device Details

"Spiesden" root tube paper needle (unsterilized)
TW: "ๅธๅฟ…็™ป" ๆ น็ฎก็ด™้‡ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

349f3ae47b272bf2ee44a2f91cb95530

DHA04401045705

Company Information

Korea, Republic of

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Root Canal Paper Needle (F.3830)".

F Dentistry

F.3830 Root Canal

import

Dates and Status

Jun 08, 2011

Jun 08, 2016

Jul 31, 2018

Cancellation Information

Logged out

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