Pure Global

“HUMAN TECH” Endosseous dental implant instrument (Non-Sterile) - Taiwan Registration c3a1b0029ac19f5374f898910e311665

Access comprehensive regulatory information for “HUMAN TECH” Endosseous dental implant instrument (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 c3a1b0029ac19f5374f898910e311665 and manufactured by HUMANTECH GERMANY GMBH. The authorized representative in Taiwan is DENTAL EASE 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
c3a1b0029ac19f5374f898910e311665
Registration Details
Taiwan FDA Registration: c3a1b0029ac19f5374f898910e311665
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“HUMAN TECH” Endosseous dental implant instrument (Non-Sterile)
TW: “賽門鐵克”植牙器械 (未滅菌)
Risk Class 1
MD

Registration Details

c3a1b0029ac19f5374f898910e311665

Ministry of Health Medical Device Import No. 019404

DHA09401940409

Company Information

Germany

Product Details

Limited to the first-level identification scope of the Measures for the Administration of Medical Devices "Dental Implant Attachment (F.3980)".

F Dental devices

F3980 Dental Intraosseous Implant Attachment

Imported from abroad

Dates and Status

Jul 23, 2018

Jul 23, 2023