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"Inosel" Ultrasound system for diagnostics - Taiwan Registration dc4e85177a62056e1f71aa2112573c7e

Access comprehensive regulatory information for "Inosel" Ultrasound system for diagnostics in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dc4e85177a62056e1f71aa2112573c7e and manufactured by Jiastar Technology Co., Ltd. Double Star Factory 2. The authorized representative in Taiwan is QISDA CORPORATION.

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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dc4e85177a62056e1f71aa2112573c7e
Registration Details
Taiwan FDA Registration: dc4e85177a62056e1f71aa2112573c7e
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Device Details

"Inosel" Ultrasound system for diagnostics
TW: โ€œไผŠ่ซพ่ณฝโ€ ่จบๆ–ท็”จ่ถ…้Ÿณๆณข็ณป็ตฑ
Risk Class 2

Registration Details

dc4e85177a62056e1f71aa2112573c7e

DHY05500586903

Company Information

Taiwan, Province of China

Product Details

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

P Radiology Science

P.1550 Ultrasonic pulsating Duppler imaging system

Medical equipment produced in bonded factories; Domestic

Dates and Status

Sep 15, 2017

Sep 15, 2027