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“SIEMENS” Diagnostic Ultrasound System - Taiwan Registration 39085fcf824b12945ca636756f9adf7f

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 39085fcf824b12945ca636756f9adf7f 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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39085fcf824b12945ca636756f9adf7f
Registration Details
Taiwan FDA Registration: 39085fcf824b12945ca636756f9adf7f
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Device Details

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

Registration Details

39085fcf824b12945ca636756f9adf7f

Ministry of Health Medical Device Import No. 027585

DHA05602758502

Company Information

Korea, Republic of

Product Details

P Devices for radiology

P1550 ultrasonic pulsating Doppler imaging system

Imported from abroad

Dates and Status

Aug 10, 2015

Aug 10, 2020

May 19, 2022

Cancellation Information

Logged out

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