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“KONICA MINOLTA” DIRECT DIGITIZER - Taiwan Registration 02bed52f946d532131e74e46efea3c24

Access comprehensive regulatory information for “KONICA MINOLTA” DIRECT DIGITIZER in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 02bed52f946d532131e74e46efea3c24 and manufactured by Konica Minolta Technoproducts Co., Ltd.. The authorized representative in Taiwan is MEDEPOCH TRADING 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.

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02bed52f946d532131e74e46efea3c24
Registration Details
Taiwan FDA Registration: 02bed52f946d532131e74e46efea3c24
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Device Details

“KONICA MINOLTA” DIRECT DIGITIZER
TW: “柯尼卡美能達”醫學影像數位器
Risk Class 2
MD

Registration Details

02bed52f946d532131e74e46efea3c24

Ministry of Health Medical Device Import No. 030181

DHA05603018101

Company Information

Product Details

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

P Devices for radiology

P1650 fluoroscopic X-ray image intensifier

Imported from abroad

Dates and Status

Sep 06, 2017

Sep 06, 2022