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“Brainlab” iPlan Treatment Planning system - Taiwan Registration bb4d6af3e5643fa11ea8294a11093826

Access comprehensive regulatory information for “Brainlab” iPlan Treatment 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 bb4d6af3e5643fa11ea8294a11093826 and manufactured by BRAINLAB AG. The authorized representative in Taiwan is WISDOM UNION ENTERPRISE CO., LTD..

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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Registration Details
Taiwan FDA Registration: bb4d6af3e5643fa11ea8294a11093826
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Device Details

“Brainlab” iPlan Treatment Planning system
TW: “博醫來”電腦治療計畫系統
Risk Class 2
MD

Registration Details

bb4d6af3e5643fa11ea8294a11093826

Ministry of Health Medical Device Import No. 032556

DHA05603255602

Company Information

Germany

Product Details

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

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Imported from abroad

Dates and Status

Apr 08, 2019

Apr 08, 2024