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"Omron" low-frequency therapy device - Taiwan Registration a56b05caadfe0e608c16f280617a426b

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 a56b05caadfe0e608c16f280617a426b and manufactured by OMRON HEALTHCARE CO., LTD. MATSUSAKA FACTORY. The authorized representative in Taiwan is OMRON HEALTHCARE TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including 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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a56b05caadfe0e608c16f280617a426b
Registration Details
Taiwan FDA Registration: a56b05caadfe0e608c16f280617a426b
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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

a56b05caadfe0e608c16f280617a426b

DHA09200098300

Company Information

Product Details

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

K Neuroscience

K.5890 Transcutaneous electrical nerve stimulator for pain relief

Contract manufacturing;; Input;; Chinese goods

Dates and Status

Feb 23, 2019

Feb 23, 2029

May 10, 2024

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