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"Siemens" ultrasonic diagnostic system - Taiwan Registration 121d77a1c6b93b9438ce4819040fe5d3

Access comprehensive regulatory information for "Siemens" ultrasonic diagnostic system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 121d77a1c6b93b9438ce4819040fe5d3 and manufactured by SIEMENS MEDICAL SOLUTIONS USA, INC.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including PANASONIC HEALTHCARE CO., LTD., Siemens Medical Solutions USA, Inc., and 3 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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121d77a1c6b93b9438ce4819040fe5d3
Registration Details
Taiwan FDA Registration: 121d77a1c6b93b9438ce4819040fe5d3
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Device Details

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

Registration Details

121d77a1c6b93b9438ce4819040fe5d3

DHA00602351303

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

May 24, 2012

May 24, 2022

Apr 12, 2024

Cancellation Information

Logged out

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