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"Rhea" ultrasound imager - Taiwan Registration dc2ed7d1ebff59866f7d5b921bc2d3b2

Access comprehensive regulatory information for "Rhea" ultrasound imager in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dc2ed7d1ebff59866f7d5b921bc2d3b2 and manufactured by ACME PORTABLE CORP.. The authorized representative in Taiwan is SWISSRAY ASIA HEALTHCARE COMPANY LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ACME PORTABLE CORP., and 1 recent registrations in the same category. 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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dc2ed7d1ebff59866f7d5b921bc2d3b2
Registration Details
Taiwan FDA Registration: dc2ed7d1ebff59866f7d5b921bc2d3b2
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Device Details

"Rhea" ultrasound imager
TW: โ€œ็‘žไบžโ€่ถ…้Ÿณๆณขๅฝฑๅƒๅ„€
Risk Class 2

Registration Details

dc2ed7d1ebff59866f7d5b921bc2d3b2

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

P Radiology Science

P.1550 Ultrasonic pulsating Duppler imaging system

Domestic;; Contract manufacturing

Dates and Status

Jun 19, 2022

Jun 19, 2027

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