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"Nippon Medical" low-frequency/vector interference wave combination therapy device - Taiwan Registration fb1992e4599cfb381e348d456a911584

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 fb1992e4599cfb381e348d456a911584 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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fb1992e4599cfb381e348d456a911584
Registration Details
Taiwan FDA Registration: fb1992e4599cfb381e348d456a911584
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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

fb1992e4599cfb381e348d456a911584

DHA05603139601

Company Information

Product Details

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

K Neuroscience;;O Physical Medical Sciences

O.5850 Powered Muscle Stimulator;; K.5890 Transcutaneous electrical nerve stimulator for pain relief

import

Dates and Status

Aug 10, 2018

Aug 10, 2028

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