Pure Global

"Kesheng" titanium system - Taiwan Registration d3876655ce0493719ce5a76b5c79a72e

Access comprehensive regulatory information for "Kesheng" titanium system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d3876655ce0493719ce5a76b5c79a72e and manufactured by CURASAN AG;; Curasan AG. The authorized representative in Taiwan is ALSTRONG SCIENTIFIC INTERNATIONAL 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
d3876655ce0493719ce5a76b5c79a72e
Registration Details
Taiwan FDA Registration: d3876655ce0493719ce5a76b5c79a72e
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Kesheng" titanium system
TW: โ€œ็ง‘็”Ÿโ€้ˆฆ็ณป็ตฑ
Risk Class 2

Registration Details

d3876655ce0493719ce5a76b5c79a72e

DHA05602992204

Company Information

Germany

Product Details

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

F Dentistry

F.4880 ้ชจๅ…งๅ›บๅฎš่žบ้‡˜ๆˆ–้‡‘ๅฑฌ็ทš

import

Dates and Status

Jun 28, 2017

Jun 28, 2027