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"Morita" potential therapy device - Taiwan Registration e7737087086490a8f005e7036934fe92

Access comprehensive regulatory information for "Morita" potential 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 e7737087086490a8f005e7036934fe92 and manufactured by Morita Kogyo Co., Ltd. Minakami Factory. The authorized representative in Taiwan is Morita Kogyo Co., Ltd. Minakami Factory.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Morita Kogyo Co., Ltd. Minakami Factory, 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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e7737087086490a8f005e7036934fe92
Registration Details
Taiwan FDA Registration: e7737087086490a8f005e7036934fe92
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Device Details

"Morita" potential therapy device
TW: โ€œๆฃฎ็”ฐโ€้›ปไฝๆฒป็™‚ๅ™จ
Risk Class 2

Registration Details

e7737087086490a8f005e7036934fe92

DHY00500276101

Company Information

Taiwan, Province of China

Product Details

Relieves stiff shoulders, headaches, chronic constipation.

o Physical Medical Sciences

O.0001 ้œ้›ปๅ™จ(้›ปไฝๆฒป็™‚ๅ™จ)

Domestic

Dates and Status

Aug 14, 2009

Aug 14, 2029

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