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Jiao Bo low frequency therapy device - Taiwan Registration dd192f0f5192e62e29809e2059caff30

Access comprehensive regulatory information for Jiao Bo 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 dd192f0f5192e62e29809e2059caff30 and manufactured by SUN-RAIN SYSTEM CORP.. The authorized representative in Taiwan is SUN-RAIN SYSTEM CORP..

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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dd192f0f5192e62e29809e2059caff30
Registration Details
Taiwan FDA Registration: dd192f0f5192e62e29809e2059caff30
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Device Details

Jiao Bo low frequency therapy device
TW: ้›ƒๅšไฝŽ้€ฑๆณขๆฒป็™‚ๅ™จ
Risk Class 2
Cancelled

Registration Details

dd192f0f5192e62e29809e2059caff30

DHY00500277502

Company Information

Taiwan, Province of China

Product Details

Relieves shoulder soreness and peripheral nerve paralysis.

K Neuroscience

K.5890 Transcutaneous electrical nerve stimulator for pain relief

Domestic

Dates and Status

Aug 31, 2009

Jul 10, 2012

Apr 16, 2014

Cancellation Information

Logged out

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