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“ASUS” Handheld Ultrasound Imaging System - Taiwan Registration f3e7f08950fd9e7d1412d437fdaf802c

Access comprehensive regulatory information for “ASUS” Handheld Ultrasound Imaging System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f3e7f08950fd9e7d1412d437fdaf802c and manufactured by ACME PORTABLE CORP.. The authorized representative in Taiwan is ASUSTEK COMPUTER INCORPORATION.

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.

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f3e7f08950fd9e7d1412d437fdaf802c
Registration Details
Taiwan FDA Registration: f3e7f08950fd9e7d1412d437fdaf802c
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Device Details

“ASUS” Handheld Ultrasound Imaging System
TW: “華碩” 手持超音波影像系統
Risk Class 2
MD

Registration Details

f3e7f08950fd9e7d1412d437fdaf802c

Ministry of Health Medical Device Manufacturing No. 007849

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

P Radiology Science

P1550 ultrasonic pulsating Doppler imaging system

Produced in Taiwan, China; Contract manufacturing

Dates and Status

May 07, 2023

May 07, 2028