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"Nippon Medical" low-frequency/vector interference wave combination therapy device - Taiwan Registration 058e6dd4296c65dd10ae9049d85a26df

Access comprehensive regulatory information for "Nippon Medical" low-frequency/vector interference wave combination 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 058e6dd4296c65dd10ae9049d85a26df and manufactured by Nihon Medix Co., Ltd. Kashiwa Factory;; DIGI I's Ltd.. The authorized representative in Taiwan is CROWNMED ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Nihon Medix Co., Ltd. Kashiwa Factory;; DIGI I's Ltd., and 1 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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058e6dd4296c65dd10ae9049d85a26df
Registration Details
Taiwan FDA Registration: 058e6dd4296c65dd10ae9049d85a26df
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Device Details

"Nippon Medical" low-frequency/vector interference wave combination therapy device
TW: โ€œๆ—ฅๆœฌ้†ซ็™‚โ€ไฝŽ้€ฑๆณข/ๅ‘้‡ๅนฒๆ“พๆณข็ต„ๅˆๆฒป็™‚ๅ„€
Risk Class 2

Registration Details

058e6dd4296c65dd10ae9049d85a26df

DHA05602912606

Company Information

Product Details

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

o Physical Medical Sciences

O.5850 5850.

import

Dates and Status

Dec 05, 2016

Dec 05, 2026

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