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“ESAOTE” Diagnostic Ultrasound System - Taiwan Registration 18bdf8cb3d3d6c331b930d1b1fe7bf7f

Access comprehensive regulatory information for “ESAOTE” Diagnostic 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 18bdf8cb3d3d6c331b930d1b1fe7bf7f and manufactured by Esaote S.p.A.. The authorized representative in Taiwan is EASTECH CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Esaote S.p.A., ESAOTE S.P.A., and 5 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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18bdf8cb3d3d6c331b930d1b1fe7bf7f
Registration Details
Taiwan FDA Registration: 18bdf8cb3d3d6c331b930d1b1fe7bf7f
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Device Details

“ESAOTE” Diagnostic Ultrasound System
TW: “百勝”超音波診斷系統
Risk Class 2
MD

Registration Details

18bdf8cb3d3d6c331b930d1b1fe7bf7f

Ministry of Health Medical Device Import No. 033310

DHA05603331001

Company Information

Italy

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 05, 2020

Mar 05, 2025

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