Taiwan FDA registration c1c07d6f752c36f7ac715f940386b684

“Mindray” Diagnostic Ultrasound System

TW: “邁瑞”可攜式彩色都卜勒超音波診斷系統
Taiwan flagTaiwan·Risk Class 2·MD·Shenzhen Mindray Bio-Medical Electronics Co., Ltd.·Registered Nov 27, 2015 – Nov 27, 2020Cancelled
Registration details
Analysis ID
c1c07d6f752c36f7ac715f940386b684
License Form
Ministry of Health Medical Device Land Transport No. 000718
Customs Code
DHA09200071804
Company information
Manufacturer Country
China
Authorized Representative
TAIWAN MEDICAL SERVICES CORPORATION
Product details
Product Type (Level 1)
P Devices for radiology
Product Type (Level 2)
P1550 ultrasonic pulsating Doppler imaging system
Import Information
Imported from abroad; Made in China
Dates and status
Registration Date
Nov 27, 2015
Expiry Date
Nov 27, 2020
Cancellation Date
Jun 16, 2022
Cancellation information
Status
Logged out
Reason
許可證已逾有效期未申請展延
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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 c1c07d6f752c36f7ac715f940386b684 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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