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"Singular" ultrasound system - Taiwan Registration 8e9168727bf2efb1855e2fced73b43b6

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 8e9168727bf2efb1855e2fced73b43b6 and manufactured by WIPRO GE HEALTHCARE PVT. LTD.. 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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8e9168727bf2efb1855e2fced73b43b6
Registration Details
Taiwan FDA Registration: 8e9168727bf2efb1855e2fced73b43b6
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Device Details

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

Registration Details

8e9168727bf2efb1855e2fced73b43b6

DHA00601862507

Company Information

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

Mar 06, 2008

Mar 06, 2023