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“KONICA MINOLTA” ULTRASOUND SYSTYEM - Taiwan Registration 4b861bbbef41a9aac7a9c0e6d00e6066

Access comprehensive regulatory information for “KONICA MINOLTA” ULTRASOUND SYSTYEM in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4b861bbbef41a9aac7a9c0e6d00e6066 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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4b861bbbef41a9aac7a9c0e6d00e6066
Registration Details
Taiwan FDA Registration: 4b861bbbef41a9aac7a9c0e6d00e6066
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Device Details

“KONICA MINOLTA” ULTRASOUND SYSTYEM
TW: “柯尼卡美能達”超音波系統
Risk Class 2
MD

Registration Details

4b861bbbef41a9aac7a9c0e6d00e6066

Ministry of Health Medical Device Import No. 030256

DHA05603025606

Company Information

Product Details

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

P Devices for radiology

P1550 ultrasonic pulsating Doppler imaging system

Imported from abroad

Dates and Status

Sep 21, 2017

Sep 21, 2027