Pure Global

“Microtek” Medical X-Ray Digitizer - Taiwan Registration e1ba30fcf920d420fc5e40b9fc8ff708

Access comprehensive regulatory information for “Microtek” Medical X-Ray Digitizer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e1ba30fcf920d420fc5e40b9fc8ff708 and manufactured by MICROTEK INTERNATIONAL INC.. The authorized representative in Taiwan is MICROTEK INTERNATIONAL INC..

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
e1ba30fcf920d420fc5e40b9fc8ff708
Registration Details
Taiwan FDA Registration: e1ba30fcf920d420fc5e40b9fc8ff708
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Microtek” Medical X-Ray Digitizer
TW: “全友”醫用X光片數位儀
Risk Class 2
MD

Registration Details

e1ba30fcf920d420fc5e40b9fc8ff708

Ministry of Health Medical Device Manufacturing No. 005654

Company Information

Taiwan, Province of China

Product Details

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

P Devices for radiology

P2050 Medical Image Management and Processing System

Produced in Taiwan, China

Dates and Status

Jan 25, 2017

Jan 25, 2027