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"Singular" ultrasound system - Taiwan Registration 57daaf692f4ee790f6d2963509846da1

Access comprehensive regulatory information for "Singular" 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 57daaf692f4ee790f6d2963509846da1 and manufactured by WIPRO GE HEALTHCARE PVT. LTD.. The authorized representative in Taiwan is GE MEDICAL SYSTEMS TAIWAN, LTD..

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including GE VINGMED ULTRASOUND AS, GE Medical Systems Israel 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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57daaf692f4ee790f6d2963509846da1
Registration Details
Taiwan FDA Registration: 57daaf692f4ee790f6d2963509846da1
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Device Details

"Singular" ultrasound system
TW: โ€œๅฅ‡็•ฐโ€่ถ…้Ÿณๆณข็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

57daaf692f4ee790f6d2963509846da1

DHA00602207401

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

P Radiology Science

P.1550 Ultrasonic pulsating Duppler imaging system

import

Dates and Status

Feb 26, 2011

Feb 26, 2021

Sep 23, 2023

Cancellation Information

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