Taiwan FDA registration ec5a831918f35359e9fbd42657775ea4

“Mindray” Diagnostic Ultrasound System

TW: “邁瑞” 可攜式彩色都卜勒超音波系統
Taiwan flagTaiwan·Risk Class 2·MD·Shenzhen Mindray Bio-Medical Electronics Co., Ltd.·Registered Oct 05, 2016 – Oct 05, 2026Active
Registration details
Analysis ID
ec5a831918f35359e9fbd42657775ea4
License Form
Ministry of Health Medical Device Land Transport No. 000784
Customs Code
DHA09200078404
Company information
Manufacturer Country
China
Authorized Representative
TAIWAN MEDICAL SERVICES CORPORATION
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
Oct 05, 2016
Expiry Date
Oct 05, 2026
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About this record

Access comprehensive regulatory information for “Mindray” 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 ec5a831918f35359e9fbd42657775ea4 and manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. The authorized representative in Taiwan is TAIWAN MEDICAL SERVICES CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Shenzhen Mindray Bio-Medical Electronics Co., Ltd., and 1 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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