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“FUJIFILM Sonosite” Edge II Ultrasound System - Taiwan Registration 89d2105f8096fbc07b72de7a0388babe

Access comprehensive regulatory information for “FUJIFILM Sonosite” Edge II 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 89d2105f8096fbc07b72de7a0388babe and manufactured by FUJIFILM SONOSITE, INC.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.

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89d2105f8096fbc07b72de7a0388babe
Registration Details
Taiwan FDA Registration: 89d2105f8096fbc07b72de7a0388babe
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Device Details

“FUJIFILM Sonosite” Edge II Ultrasound System
TW: “富士索諾聲”超音波系統
Risk Class 2
MD

Registration Details

89d2105f8096fbc07b72de7a0388babe

Ministry of Health Medical Device Import No. 029419

DHA05602941908

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 22, 2017

Mar 22, 2027