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"Keina" transcutaneous electrical nerve stimulator - Taiwan Registration 94d3a55ac4535ba50e598acfebb51fa4

Access comprehensive regulatory information for "Keina" transcutaneous electrical nerve stimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 94d3a55ac4535ba50e598acfebb51fa4 and manufactured by Qingming Medical Equipment Co., Ltd. Wugu Factory. The authorized representative in Taiwan is Qingming Medical Equipment Co., Ltd. Wugu Factory.

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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94d3a55ac4535ba50e598acfebb51fa4
Registration Details
Taiwan FDA Registration: 94d3a55ac4535ba50e598acfebb51fa4
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Device Details

"Keina" transcutaneous electrical nerve stimulator
TW: "ๆ…ถๅ" ็ถ“็šฎ็ฅž็ถ“้›ปๅˆบๆฟ€ๅ™จ
Risk Class 2

Registration Details

94d3a55ac4535ba50e598acfebb51fa4

DHY00500114704

Company Information

Product Details

K Neuroscience

Domestic

Dates and Status

Jul 12, 2004

Jul 12, 2029