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“Deymed” repetitive Transcranial Magnetic Stimulator Therapy System - Taiwan Registration 6946b0365271473b6f660a1398fed0e2

Access comprehensive regulatory information for “Deymed” repetitive Transcranial Magnetic Stimulator Therapy System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6946b0365271473b6f660a1398fed0e2 and manufactured by Deymed Diagnostic s.r.o.. The authorized representative in Taiwan is Onemed 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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6946b0365271473b6f660a1398fed0e2
Registration Details
Taiwan FDA Registration: 6946b0365271473b6f660a1398fed0e2
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Device Details

“Deymed” repetitive Transcranial Magnetic Stimulator Therapy System
TW: “萬美德”重覆式經顱磁刺激治療系統
Risk Class 2
MD

Registration Details

6946b0365271473b6f660a1398fed0e2

Ministry of Health Medical Device Import No. 035167

DHA05603516706

Company Information

Czechia

Product Details

Details are as detailed as approved Chinese instructions

K Neuroscience

K5805 Repetitive Transcranial Magnetic Stimulation (rTMS) Treatment System

Imported from abroad

Dates and Status

Jan 03, 2022

Jan 03, 2027