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“SIEMENS” Diagnostic Ultrasound System - Taiwan Registration 7df683f4fe9028c5db56e5165b689825

Access comprehensive regulatory information for “SIEMENS” Diagnostic Ultrasound System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7df683f4fe9028c5db56e5165b689825 and manufactured by Siemens Healthineers Ltd.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including Siemens Healthineers Ltd., Siemens Healthcare Ltd., 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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7df683f4fe9028c5db56e5165b689825
Registration Details
Taiwan FDA Registration: 7df683f4fe9028c5db56e5165b689825
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Device Details

“SIEMENS” Diagnostic Ultrasound System
TW: “西門子”超音波系統
Risk Class 2
MD

Registration Details

7df683f4fe9028c5db56e5165b689825

Ministry of Health Medical Device Import No. 028621

DHA05602862101

Company Information

Korea, Republic of

Product Details

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

P Devices for radiology

P1550 ultrasonic pulsating Doppler imaging system

Imported from abroad

Dates and Status

Jul 11, 2016

Jul 11, 2026