Pure Global

“NEXOBIO ” Transcen Temporary Light Cured Resin - Taiwan Registration 62218ade9a730df294131c21078f3700

Access comprehensive regulatory information for “NEXOBIO ” Transcen Temporary Light Cured Resin in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 62218ade9a730df294131c21078f3700 and manufactured by NEXOBIO Co., Ltd.. The authorized representative in Taiwan is HSIN HUI MEDICAL 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
62218ade9a730df294131c21078f3700
Registration Details
Taiwan FDA Registration: 62218ade9a730df294131c21078f3700
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“NEXOBIO ” Transcen Temporary Light Cured Resin
TW: “奈梭拜耳”傳勝臨時牙冠和牙橋樹脂
Risk Class 2
MD

Registration Details

62218ade9a730df294131c21078f3700

Ministry of Health Medical Device Import No. 028665

DHA05602866505

Company Information

Korea, Republic of

Product Details

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

F Dental devices

F3770 Temporary crown and bridge resin

Imported from abroad

Dates and Status

Jun 15, 2016

Jun 15, 2026