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“KONICA MINOLTA”Direct Digitizer SKR 3000 - Taiwan Registration 3fe643601b23d946874e486d83dae3c9

Access comprehensive regulatory information for “KONICA MINOLTA”Direct Digitizer SKR 3000 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3fe643601b23d946874e486d83dae3c9 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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3fe643601b23d946874e486d83dae3c9
Registration Details
Taiwan FDA Registration: 3fe643601b23d946874e486d83dae3c9
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Device Details

“KONICA MINOLTA”Direct Digitizer SKR 3000
TW: “柯尼卡美能達”數位X光成像系統
Risk Class 2
MD

Registration Details

3fe643601b23d946874e486d83dae3c9

Ministry of Health Medical Device Import No. 035514

DHA05603551401

Company Information

Product Details

Details are as detailed as approved Chinese instructions

P Radiology Science

P1650 fluoroscopic X-ray image intensifier

Imported from abroad

Dates and Status

Jun 28, 2022

Jun 28, 2027