Taiwan FDA registration c3a1b0029ac19f5374f898910e311665

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

TW: “賽門鐵克”植牙器械 (未滅菌)

Taiwan·Risk Class 1·MD·HUMANTECH GERMANY GMBH·Registered Jul 23, 2018 – Jul 23, 2023Expired

Registration details

Analysis ID: c3a1b0029ac19f5374f898910e311665
License Form: Ministry of Health Medical Device Import No. 019404
Customs Code: DHA09401940409

Company information

Manufacturer: HUMANTECH GERMANY GMBH
Manufacturer Country: Germany
Authorized Representative: DENTAL EASE TECHNOLOGY CO., LTD.

Product details

Intended Use: Limited to the first-level identification scope of the Measures for the Administration of Medical Devices "Dental Implant Attachment (F.3980)".
Product Type (Level 1): F Dental devices
Product Type (Level 2): F3980 Dental Intraosseous Implant Attachment
Import Information: Imported from abroad

Dates and status

Registration Date: Jul 23, 2018
Expiry Date: Jul 23, 2023

About this record

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.