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“Philips” Radiation Therapy Planning System - Taiwan Registration b034c5c9fb77f176258c0fd0791b6143

Access comprehensive regulatory information for “Philips” Radiation Therapy Planning System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b034c5c9fb77f176258c0fd0791b6143 and manufactured by PHILIPS MEDICAL SYSTEMS(CLEVELAND),INC.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including PHILIPS MEDICAL SYSTEMS(CLEVELAND),INC., 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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b034c5c9fb77f176258c0fd0791b6143
Registration Details
Taiwan FDA Registration: b034c5c9fb77f176258c0fd0791b6143
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Device Details

“Philips” Radiation Therapy Planning System
TW: “飛利浦”放射治療模擬計畫系統
Risk Class 2
MD

Registration Details

b034c5c9fb77f176258c0fd0791b6143

Ministry of Health Medical Device Import No. 026936

DHA05602693600

Company Information

Product Details

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

P Devices for radiology

P5840 Radiation Therapy Simulation System

Imported from abroad

Dates and Status

Jan 13, 2015

Jan 13, 2025

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