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“Siemens” Diagnostic Ultrasound System - Taiwan Registration f278c1106b18f4f4b3dbbe08b8aaaf15

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 f278c1106b18f4f4b3dbbe08b8aaaf15 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, 3 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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f278c1106b18f4f4b3dbbe08b8aaaf15
Registration Details
Taiwan FDA Registration: f278c1106b18f4f4b3dbbe08b8aaaf15
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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

f278c1106b18f4f4b3dbbe08b8aaaf15

Ministry of Health Medical Device Import No. 030778

DHA05603077800

Company Information

United States

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

Mar 21, 2018

Mar 21, 2023