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"Ouju" low-frequency therapy device - Taiwan Registration e51de1a175c4e51edc83621787441297

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 e51de1a175c4e51edc83621787441297 and manufactured by OG Wellness Technologies 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 AND GIKEN CO., LTD., AND GIKEN CO., LTD., OKU FACTORY, 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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e51de1a175c4e51edc83621787441297
Registration Details
Taiwan FDA Registration: e51de1a175c4e51edc83621787441297
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Device Details

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

Registration Details

e51de1a175c4e51edc83621787441297

DHA00602092501

Company Information

Product Details

Promote local blood circulation, relieve shoulder pain and peripheral nerve paralysis.

K Neuroscience

K.5890 Transcutaneous electrical nerve stimulator for pain relief

import

Dates and Status

Apr 21, 2010

Apr 21, 2020

May 19, 2022

Cancellation Information

Logged out

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