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"Omron" low-frequency therapy device - Taiwan Registration d32ae2e0ba952841ee635635bdaf1d38

Access comprehensive regulatory information for "Omron" low-frequency therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d32ae2e0ba952841ee635635bdaf1d38 and manufactured by OMRON HEALTHCARE MANUFACTURING VIETNAM CO., LTD.;; OMRON HEALTHCARE CO., LTD.. The authorized representative in Taiwan is OMRON HEALTHCARE TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including OMRON HEALTHCARE CO., LTD. MATSUSAKA FACTORY, OMRON HEALTHCARE MANUFACTURING VIETNAM CO., LTD.;; OMRON HEALTHCARE CO., LTD., and 2 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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d32ae2e0ba952841ee635635bdaf1d38
Registration Details
Taiwan FDA Registration: d32ae2e0ba952841ee635635bdaf1d38
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Device Details

"Omron" low-frequency therapy device
TW: โ€œๆญๅง†้พโ€ไฝŽ้€ฑๆณขๆฒป็™‚ๅ™จ
Risk Class 2

Registration Details

d32ae2e0ba952841ee635635bdaf1d38

DHA05603719508

Product Details

Details are as detailed as approved Chinese instructions

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Dates and Status

Jun 06, 2024

Jun 06, 2029