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“Siemens” Diagnostic Ultrasound System - Taiwan Registration f4eb45675db126a260c2a5f74812e356

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 f4eb45675db126a260c2a5f74812e356 and manufactured by Siemens Healthcare 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 Medical Solutions USA, Inc., 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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f4eb45675db126a260c2a5f74812e356
Registration Details
Taiwan FDA Registration: f4eb45675db126a260c2a5f74812e356
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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

f4eb45675db126a260c2a5f74812e356

Ministry of Health Medical Device Import No. 031222

DHA05603122207

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 24, 2018

Jul 24, 2028