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“Brainsway” Deep TMS System and Accessories - Taiwan Registration 0a7e9c1e3d25e62c80049d7c503cf249

Access comprehensive regulatory information for “Brainsway” Deep TMS System and Accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0a7e9c1e3d25e62c80049d7c503cf249 and manufactured by Brainsway Ltd.. The authorized representative in Taiwan is UNISON COMPANY 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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0a7e9c1e3d25e62c80049d7c503cf249
Registration Details
Taiwan FDA Registration: 0a7e9c1e3d25e62c80049d7c503cf249
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Device Details

“Brainsway” Deep TMS System and Accessories
TW: “智道”重複式經顱磁刺激治療系統及配件
Risk Class 2
MD

Registration Details

0a7e9c1e3d25e62c80049d7c503cf249

Ministry of Health Medical Device Import No. 034433

DHA05603443309

Company Information

Israel

Product Details

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

K Devices for neuroscience

K5805 Repetitive Transcranial Magnetic Stimulation (rTMS) Treatment System

Imported from abroad

Dates and Status

Apr 16, 2021

Apr 16, 2026