Pure Global

“FUJIFILM” COMPUTED RADIOGRAPHY XG5000 PLUS - Taiwan Registration ce19879a66416f9b27a93aeb707a1500

Access comprehensive regulatory information for “FUJIFILM” COMPUTED RADIOGRAPHY XG5000 PLUS in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ce19879a66416f9b27a93aeb707a1500 and manufactured by FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE. The authorized representative in Taiwan is NAN KAI CORPORATION.

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
ce19879a66416f9b27a93aeb707a1500
Registration Details
Taiwan FDA Registration: ce19879a66416f9b27a93aeb707a1500
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“FUJIFILM” COMPUTED RADIOGRAPHY XG5000 PLUS
TW: “富士”電腦X光影像讀取儀
Risk Class 2
MD
Cancelled

Registration Details

ce19879a66416f9b27a93aeb707a1500

Ministry of Health Medical Device Import No. 026454

DHA05602645408

Company Information

Product Details

P Devices for radiology

P1650 fluoroscopic X-ray image intensifier

Imported from abroad

Dates and Status

Aug 28, 2014

Aug 28, 2019

Jun 22, 2022

Cancellation Information

Logged out

許可證已逾有效期