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“KONICA MINOLTA” Imaging Diagnostic Workstation DI-X1 - Taiwan Registration e3dee9bf191ee29ec4a9fc8f0fb8a744

Access comprehensive regulatory information for “KONICA MINOLTA” Imaging Diagnostic Workstation DI-X1 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e3dee9bf191ee29ec4a9fc8f0fb8a744 and manufactured by Konica Minolta Technoproducts Co., Ltd.. The authorized representative in Taiwan is QUALTECH CONSULTING 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.

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e3dee9bf191ee29ec4a9fc8f0fb8a744
Registration Details
Taiwan FDA Registration: e3dee9bf191ee29ec4a9fc8f0fb8a744
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Device Details

“KONICA MINOLTA” Imaging Diagnostic Workstation DI-X1
TW: “柯尼卡美能達” 影像診斷工作站
Risk Class 2
MD

Registration Details

e3dee9bf191ee29ec4a9fc8f0fb8a744

Ministry of Health Medical Device Import No. 036342

DHA05603634203

Company Information

Product Details

Details are as detailed as approved Chinese instructions

P Radiology Science

P2050 Medical Image Management and Processing System

Imported from abroad

Dates and Status

Apr 04, 2023

Apr 04, 2028