Taiwan FDA registration afc322d1da03190f278bfbede2218658

“RTD” Corecem Dual Cure Resin Cement and Core Build-up Composite

TW: “雷泰德”克爾森雙向固化樹脂黏著劑暨冠心堆築複合樹脂
Taiwan flagTaiwan·Risk Class 2·MD·RTD·Registered Jun 26, 2015 – Jun 26, 2025Expired
Registration details
Analysis ID
afc322d1da03190f278bfbede2218658
License Form
Ministry of Health Medical Device Import No. 027481
Customs Code
DHA05602748103
Company information
Manufacturer
RTD
Manufacturer Country
France
Authorized Representative
SHI SEI INTERNATIONAL LIMITED
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
F Dental devices
Product Type (Level 2)
F3690 Resin tusk wood
Import Information
Imported from abroad
Dates and status
Registration Date
Jun 26, 2015
Expiry Date
Jun 26, 2025
About this record

Access comprehensive regulatory information for “RTD” Corecem Dual Cure Resin Cement and Core Build-up Composite in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number afc322d1da03190f278bfbede2218658 and manufactured by RTD. The authorized representative in Taiwan is SHI SEI INTERNATIONAL LIMITED.

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 DatabasePowered by Pure Global AI89,000+ Devices