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"Kaishen" transcutaneous electronic neurostimulator - Taiwan Registration 57af81ee442991095f2e1995bb6c5220

Access comprehensive regulatory information for "Kaishen" transcutaneous electronic neurostimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 57af81ee442991095f2e1995bb6c5220 and manufactured by Kaishen Limited. The authorized representative in Taiwan is Kaishen Limited.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Kaishen Limited, and 1 recent registrations in the same category. 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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57af81ee442991095f2e1995bb6c5220
Registration Details
Taiwan FDA Registration: 57af81ee442991095f2e1995bb6c5220
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Device Details

"Kaishen" transcutaneous electronic neurostimulator
TW: "ๅ•Ÿ็”ณ"็ถ“็šฎ้›ปๅญ็ฅž็ถ“ๅˆบๆฟ€ๅ™จ
Risk Class 2

Registration Details

57af81ee442991095f2e1995bb6c5220

DHY00500077502

Company Information

Taiwan, Province of China

Product Details

1899 Other physical and therapeutic equipment

Domestic

Dates and Status

Apr 27, 1999

Feb 09, 2029

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