Taiwan FDA registration f4eb45675db126a260c2a5f74812e356

“Siemens” Diagnostic Ultrasound System

TW: “西門子”超音波系統
Taiwan flagTaiwan·Risk Class 2·MD·Siemens Healthcare Ltd.·Registered Jul 24, 2018 – Jul 24, 2028Active
Registration details
Analysis ID
f4eb45675db126a260c2a5f74812e356
License Form
Ministry of Health Medical Device Import No. 031222
Customs Code
DHA05603122207
Company information
Manufacturer Country
Korea, Republic of
Authorized Representative
SIEMENS HEALTHCARE LIMITED
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
P Devices for radiology
Product Type (Level 2)
P1550 ultrasonic pulsating Doppler imaging system
Import Information
Imported from abroad
Dates and status
Registration Date
Jul 24, 2018
Expiry Date
Jul 24, 2028
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About this record

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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