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“FUJIFILM SonoSite” Edge Diagnostic Doppler Ultrasound System - Taiwan Registration 582e2a1e3ead4666711565d588894c96

Access comprehensive regulatory information for “FUJIFILM SonoSite” Edge Diagnostic Doppler 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 582e2a1e3ead4666711565d588894c96 and manufactured by FUJIFILM SONOSITE, INC.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.

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582e2a1e3ead4666711565d588894c96
Registration Details
Taiwan FDA Registration: 582e2a1e3ead4666711565d588894c96
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Device Details

“FUJIFILM SonoSite” Edge Diagnostic Doppler Ultrasound System
TW: “富士索諾聲”數位彩色超音波掃描器
Risk Class 2
MD

Registration Details

582e2a1e3ead4666711565d588894c96

Ministry of Health Medical Device Import No. 026025

DHA05602602501

Company Information

United States

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 25, 2014

Mar 25, 2024