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"Siemens" ultrasonic diagnostic system - Taiwan Registration 21a9594e55aa9b984e165099c9bb5869

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 21a9594e55aa9b984e165099c9bb5869 and manufactured by PANASONIC HEALTHCARE CO., LTD.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including SIEMENS MEDICAL SOLUTIONS USA, INC., PANASONIC HEALTHCARE CO., LTD., 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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21a9594e55aa9b984e165099c9bb5869
Registration Details
Taiwan FDA Registration: 21a9594e55aa9b984e165099c9bb5869
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Device Details

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

Registration Details

21a9594e55aa9b984e165099c9bb5869

DHA00601795701

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 26, 2007

Mar 26, 2017

Nov 04, 2019

Cancellation Information

Logged out

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