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"Ouju" low-frequency therapy device - Taiwan Registration c3ee4b176cb14c84fd17283033031e0d

Access comprehensive regulatory information for "Ouju" 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 c3ee4b176cb14c84fd17283033031e0d and manufactured by AND GIKEN CO., LTD., OKU FACTORY. The authorized representative in Taiwan is AMPLE MEDICAL INSTRUMENTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including OG Wellness Technologies CO., LTD., OKU FACTORY, AND GIKEN 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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Registration Details
Taiwan FDA Registration: c3ee4b176cb14c84fd17283033031e0d
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Device Details

"Ouju" low-frequency therapy device
TW: โ€œๆญๅฑ…โ€ไฝŽ้€ฑๆณขๆฒป็™‚ๅ„€
Risk Class 2
Cancelled

Registration Details

c3ee4b176cb14c84fd17283033031e0d

DHA00602109402

Company Information

Product Details

Relieves shoulder pain and peripheral nerve paralysis, and promotes local blood circulation.

K Neuroscience

K.5890 Transcutaneous electrical nerve stimulator for pain relief

import

Dates and Status

Jun 11, 2010

Jun 11, 2015

Jul 31, 2018

Cancellation Information

Logged out

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