Taiwan FDA registration 7d901a9d7774e2522d6511397a42438d

“Philips” EPIQ Series Diagnostic Ultrasound Systems

TW: “飛利浦” 超音波系統
Taiwan flagTaiwan·Risk Class 2·MD·For use only by the Parts System Denda;;For spare parts system only;;Philips Ultrasound, LLC·Registered Jul 07, 2021 – Jul 07, 2026Expired
Registration details
Analysis ID
7d901a9d7774e2522d6511397a42438d
License Form
Ministry of Health Medical Device Import No. 034753
Customs Code
DHA05603475301
Company information
Manufacturer Country
China;;United States
Authorized Representative
PHILIPS TAIWAN LIMITED
Product details
Intended Use
Details are as detailed as approved Chinese instructions
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 07, 2021
Expiry Date
Jul 07, 2026
About this record

Access comprehensive regulatory information for “Philips” EPIQ Series Diagnostic Ultrasound Systems in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7d901a9d7774e2522d6511397a42438d and manufactured by For use only by the Parts System Denda;;For spare parts system only;;Philips Ultrasound, LLC. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

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