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“Deymed” Magnetic Stimulator - Taiwan Registration 93401918d0e5afb8a427a7979688f845

Access comprehensive regulatory information for “Deymed” Magnetic Stimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 93401918d0e5afb8a427a7979688f845 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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93401918d0e5afb8a427a7979688f845
Registration Details
Taiwan FDA Registration: 93401918d0e5afb8a427a7979688f845
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Device Details

“Deymed” Magnetic Stimulator
TW: “萬美德”磁波刺激器
Risk Class 2
MD

Registration Details

93401918d0e5afb8a427a7979688f845

Ministry of Health Medical Device Import No. 036547

DHA05603654708

Company Information

Czechia

Product Details

Details are as detailed as approved Chinese instructions

K Neuroscience

K1870 Evoked reactive electrical stimulator

Imported from abroad

Dates and Status

Jun 20, 2023

Jun 20, 2028