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"Japanese Medical" low-frequency therapy device - Taiwan Registration 4dae66c776169e81c2f1f0ff9ed4a82e

Access comprehensive regulatory information for "Japanese Medical" 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 4dae66c776169e81c2f1f0ff9ed4a82e and manufactured by NIHON MEDIX CO., LTD. KASHIWA FACTORY. 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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4dae66c776169e81c2f1f0ff9ed4a82e
Registration Details
Taiwan FDA Registration: 4dae66c776169e81c2f1f0ff9ed4a82e
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Device Details

"Japanese Medical" low-frequency therapy device
TW: โ€œๆ—ฅๆœฌ้†ซ็™‚โ€ไฝŽ้€ฑๆณขๆฒป็™‚ๅ„€
Risk Class 2

Registration Details

4dae66c776169e81c2f1f0ff9ed4a82e

DHA00602483606

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

import

Dates and Status

Apr 01, 2013

Apr 01, 2028

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