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"Hanwo" watch-type low-frequency therapy device - Taiwan Registration 6205d20a8bba7265f66ca0cca9af697f

Access comprehensive regulatory information for "Hanwo" watch-type 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 6205d20a8bba7265f66ca0cca9af697f 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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6205d20a8bba7265f66ca0cca9af697f
Registration Details
Taiwan FDA Registration: 6205d20a8bba7265f66ca0cca9af697f
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Device Details

"Hanwo" watch-type low-frequency therapy device
TW: "็ฟฐๆฒƒ" ๆ‰‹้Œถๅž‹ไฝŽ้€ฑๆณขๆฒป็™‚ๅ™จ
Risk Class 2
Cancelled

Registration Details

6205d20a8bba7265f66ca0cca9af697f

DHY00500153704

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 18, 2005

Oct 18, 2020

Jun 22, 2022

Cancellation Information

Logged out

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