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“Philips” Data Management System - Taiwan Registration 6f9dc450024f829e2fd73fb9c8087b92

Access comprehensive regulatory information for “Philips” Data Management System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6f9dc450024f829e2fd73fb9c8087b92 and manufactured by Philips Ultrasound, LLC. The authorized representative in Taiwan is PHILIPS TAIWAN 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.

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6f9dc450024f829e2fd73fb9c8087b92
Registration Details
Taiwan FDA Registration: 6f9dc450024f829e2fd73fb9c8087b92
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Device Details

“Philips” Data Management System
TW: “飛利浦”資料處理系統
Risk Class 2
MD

Registration Details

6f9dc450024f829e2fd73fb9c8087b92

Ministry of Health Medical Device Import No. 026577

DHA05602657701

Company Information

United States

Product Details

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

P Devices for radiology

P2050 Medical Image Management and Processing System

Imported from abroad

Dates and Status

Sep 25, 2014

Sep 25, 2024