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"Hanwo" Ruyi Low Frequency Therapy Device - Taiwan Registration c1a89609a63f0c267c47954400a9c33e

Access comprehensive regulatory information for "Hanwo" Ruyi 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 c1a89609a63f0c267c47954400a9c33e and manufactured by HIVOX BIOTEK INC.. The authorized representative in Taiwan is HIVOX BIOTEK INC..

This page provides complete technical specifications, regulatory compliance details. 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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c1a89609a63f0c267c47954400a9c33e
Registration Details
Taiwan FDA Registration: c1a89609a63f0c267c47954400a9c33e
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Device Details

"Hanwo" Ruyi Low Frequency Therapy Device
TW: "็ฟฐๆฒƒ" ๅฆ‚ๆ„่ฒผไฝŽๅ‘จๆณขๆฒป็™‚ๅ™จ
Risk Class 2
Cancelled

Registration Details

c1a89609a63f0c267c47954400a9c33e

DHY00500150109

Company Information

Taiwan, Province of China

Product Details

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

K Neuroscience

K.5890 Transcutaneous electrical nerve stimulator for pain relief

Domestic

Dates and Status

Oct 04, 2005

Oct 04, 2020

Jun 22, 2022

Cancellation Information

Logged out

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