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“KONICA MINOLTA” ULTRASOUND SYSTEM - Taiwan Registration 61bed1b90e1197eb730750cac3c627e6

Access comprehensive regulatory information for “KONICA MINOLTA” ULTRASOUND SYSTEM in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 61bed1b90e1197eb730750cac3c627e6 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, 1 companies making similar products including KONICA MINOLTA TECHNOPRODUCTS CO., LTD., and 1 recent registrations in the same category. 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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61bed1b90e1197eb730750cac3c627e6
Registration Details
Taiwan FDA Registration: 61bed1b90e1197eb730750cac3c627e6
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Device Details

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

Registration Details

61bed1b90e1197eb730750cac3c627e6

Ministry of Health Medical Device Import No. 032289

DHA05603228905

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

Mar 08, 2019

Mar 08, 2024

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