Pure Global

“Siemens”Ultrasonic imaging System - Taiwan Registration dcb28993e7cdfbfc7eb90df6199cc114

Access comprehensive regulatory information for “Siemens”Ultrasonic imaging System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dcb28993e7cdfbfc7eb90df6199cc114 and manufactured by Siemens Healthineers Ltd.. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

This page provides complete technical specifications, regulatory compliance details. 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
dcb28993e7cdfbfc7eb90df6199cc114
Registration Details
Taiwan FDA Registration: dcb28993e7cdfbfc7eb90df6199cc114
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Siemens”Ultrasonic imaging System
TW: “西門子”診斷用超音波系統
Risk Class 2
MD

Registration Details

dcb28993e7cdfbfc7eb90df6199cc114

Department of Health Medical Device Import No. 019691

DHA00601969102

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

Mar 06, 2009

Mar 06, 2024