Taiwan FDA registration 8936b85aaf6129e389c1dc9f4172b874

"Rhea" ultrasound imager

TW: “瑞亞”超音波影像儀
Taiwan flagTaiwan·Risk Class 2·ACME PORTABLE CORP.·Registered Jan 25, 2021 – May 07, 2025Expired
Registration details
Analysis ID
8936b85aaf6129e389c1dc9f4172b874
Company information
Manufacturer Country
Taiwan, Province of China
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
P Radiology Science
Product Type (Level 2)
P.1550 Ultrasonic pulsating Duppler imaging system
Import Information
Contract manufacturing;; Domestic
Dates and status
Registration Date
Jan 25, 2021
Expiry Date
May 07, 2025
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About this record

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 8936b85aaf6129e389c1dc9f4172b874 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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