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“FUJIFILM Sonosite” SII Ultrasound System - Taiwan Registration 6fcf2bd05bbcbad33c091aead5471af4

Access comprehensive regulatory information for “FUJIFILM Sonosite” SII 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 6fcf2bd05bbcbad33c091aead5471af4 and manufactured by FUJIFILM SONOSITE, INC.. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.

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6fcf2bd05bbcbad33c091aead5471af4
Registration Details
Taiwan FDA Registration: 6fcf2bd05bbcbad33c091aead5471af4
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Device Details

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

Registration Details

6fcf2bd05bbcbad33c091aead5471af4

Ministry of Health Medical Device Import No. 029429

DHA05602942901

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 30, 2017

Mar 30, 2027