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“HITACHI” Digital Diagnostic Ultrasound Scanner - Taiwan Registration e4bbfa096cf6f0cbd6786a7ba15d8117

Access comprehensive regulatory information for “HITACHI” Digital Diagnostic Ultrasound Scanner in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e4bbfa096cf6f0cbd6786a7ba15d8117 and manufactured by Hitachi Healthcare Manufacturing, Ltd. Analytical Systems Kashiwa Factory. The authorized representative in Taiwan is Taiwan Health Fujifilm Medical Equipment Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Hitachi, Ltd. Medical System Operations Group, Kashiwa, 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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e4bbfa096cf6f0cbd6786a7ba15d8117
Registration Details
Taiwan FDA Registration: e4bbfa096cf6f0cbd6786a7ba15d8117
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Device Details

“HITACHI” Digital Diagnostic Ultrasound Scanner
TW: “日立”超音波掃描儀
Risk Class 2
MD

Registration Details

e4bbfa096cf6f0cbd6786a7ba15d8117

Ministry of Health Medical Device Import No. 026440

DHA05602644000

Product Details

P Devices for radiology

P1550 ultrasonic pulsating Doppler imaging system

Imported from abroad

Dates and Status

Aug 19, 2014

Aug 19, 2024

Mar 08, 2023

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