Taiwan FDA registration 61bed1b90e1197eb730750cac3c627e6

“KONICA MINOLTA” ULTRASOUND SYSTEM

TW: “柯尼卡美能達”超音波系統
Taiwan flagTaiwan·Risk Class 2·MD·Konica Minolta Technoproducts Co., Ltd.·Registered Mar 08, 2019 – Mar 08, 2024Expired
Registration details
Analysis ID
61bed1b90e1197eb730750cac3c627e6
License Form
Ministry of Health Medical Device Import No. 032289
Customs Code
DHA05603228905
Company information
Manufacturer Country
Japan
Authorized Representative
QUALTECH CONSULTING CORPORATION
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
P Devices for radiology
Product Type (Level 2)
P1550 ultrasonic pulsating Doppler imaging system
Import Information
Imported from abroad
Dates and status
Registration Date
Mar 08, 2019
Expiry Date
Mar 08, 2024
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About this record

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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