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"Singular" ultrasound system - Taiwan Registration c31e37127a9f1ce7a257d5465ce4d813

Access comprehensive regulatory information for "Singular" 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 c31e37127a9f1ce7a257d5465ce4d813 and manufactured by GE Medical Systems Imformation Technologies โ€“ Critikon De Mexico S. De R.L. De C.V.;; GE Medical Systems Ultrasound & Primary Care Diagnostics LLC. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including WIPRO GE HEALTHCARE PVT. LTD., GE VINGMED ULTRASOUND AS, and 5 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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c31e37127a9f1ce7a257d5465ce4d813
Registration Details
Taiwan FDA Registration: c31e37127a9f1ce7a257d5465ce4d813
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Device Details

"Singular" ultrasound system
TW: โ€œๅฅ‡็•ฐโ€่ถ…้Ÿณๆณข็ณป็ตฑ
Risk Class 2

Registration Details

c31e37127a9f1ce7a257d5465ce4d813

DHA05603187500

Product Details

For details, it is Chinese approved copy of the imitation order

P Radiology Science

P.1550 Ultrasonic pulsating Duppler imaging system

import

Dates and Status

Dec 21, 2018

Dec 21, 2028