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"Siemens" ultrasonic system - Taiwan Registration ee7be885b64bd63cd959bbd796eff109

Access comprehensive regulatory information for "Siemens" ultrasonic system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ee7be885b64bd63cd959bbd796eff109 and manufactured by SIEMENS MEDICAL SOLUTIONS USA, INC.. The authorized representative in Taiwan is SIEMENS LIMITED.

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including Siemens Medical Solutions USA, Inc.;; Siemens Healthcare s.r.o., SIEMENS MEDICAL SOLUTIONS USA, INC. ULTRASOUND DIVISION, 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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ee7be885b64bd63cd959bbd796eff109
Registration Details
Taiwan FDA Registration: ee7be885b64bd63cd959bbd796eff109
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Device Details

"Siemens" ultrasonic system
TW: โ€œ่ฅฟ้–€ๅญโ€่ถ…้Ÿณๆณข็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

ee7be885b64bd63cd959bbd796eff109

DHA00601910907

Company Information

United States

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

Jul 11, 2008

Jul 11, 2013

Aug 10, 2015

Cancellation Information

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