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"Siemens" ultrasonic system - Taiwan Registration 017b2f1b6355b381e97d31e1cc3d382c

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 017b2f1b6355b381e97d31e1cc3d382c and manufactured by Siemens Medical Solutions USA, Inc.;; Made (部分製程) in MALAYSIA;; Siemens Healthcare s.r.o.. The authorized representative in Taiwan is BEST DIGITAL CO., LTD..

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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017b2f1b6355b381e97d31e1cc3d382c
Registration Details
Taiwan FDA Registration: 017b2f1b6355b381e97d31e1cc3d382c
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Device Details

"Siemens" ultrasonic system
TW: “西門子” 超音波系統
Risk Class 2

Registration Details

017b2f1b6355b381e97d31e1cc3d382c

DHA05603690100

Company Information

Product Details

Details are as detailed as approved Chinese instructions

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P.1550 Ultrasonic pulsating Duppler imaging system

import

Dates and Status

Jan 13, 2024

Jan 13, 2029