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"Senjamei" low frequency therapy device - Taiwan Registration fee7cba08ec0d8eb577479d249326c76

Access comprehensive regulatory information for "Senjamei" 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 fee7cba08ec0d8eb577479d249326c76 and manufactured by SHIAN JIA MEEI ENTERPRISE CO., LTD.. The authorized representative in Taiwan is SHIAN JIA MEEI ENTERPRISE CO., LTD..

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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fee7cba08ec0d8eb577479d249326c76
Registration Details
Taiwan FDA Registration: fee7cba08ec0d8eb577479d249326c76
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Device Details

"Senjamei" low frequency therapy device
TW: "ไป™ไฝณ็พŽ" ไฝŽ้€ฑๆณขๆฒป็™‚ๅ™จ
Risk Class 2

Registration Details

fee7cba08ec0d8eb577479d249326c76

Company Information

Taiwan, Province of China

Product Details

K Neuroscience

Domestic

Dates and Status

Jul 17, 2003

Jul 17, 2028