“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.
This page provides complete technical specifications, regulatory compliance details. 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.
Device Details
Registration Details
582e2a1e3ead4666711565d588894c96
Ministry of Health Medical Device Import No. 026025
DHA05602602501
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

