Pure Global

“Thommen” INICELL Implant System - Taiwan Registration f826e36c9fac4f68bdca58292867d87b

Access comprehensive regulatory information for “Thommen” INICELL Implant System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number f826e36c9fac4f68bdca58292867d87b and manufactured by THOMMEN MEDICAL AG. The authorized representative in Taiwan is EN-JYE INTERNATIONAL 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
f826e36c9fac4f68bdca58292867d87b
Registration Details
Taiwan FDA Registration: f826e36c9fac4f68bdca58292867d87b
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Thommen” INICELL Implant System
TW: “拓美”植體系統
Risk Class 3
MD

Registration Details

f826e36c9fac4f68bdca58292867d87b

Ministry of Health Medical Device Import No. 025953

DHA05602595308

Company Information

Switzerland

Product Details

For details, it is Chinese approved copy of the imitation order

F Dental devices

F3640 Bone explants

Imported from abroad

Dates and Status

Mar 10, 2014

Mar 10, 2024