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"Morita" potential therapy device - Taiwan Registration fa1c550160e967bec6054a43efd464c4

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 fa1c550160e967bec6054a43efd464c4 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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fa1c550160e967bec6054a43efd464c4
Registration Details
Taiwan FDA Registration: fa1c550160e967bec6054a43efd464c4
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Device Details

"Morita" potential therapy device
TW: "ๆฃฎ็”ฐ"้›ปไฝๆฒป็™‚ๅ™จ
Risk Class 2

Registration Details

fa1c550160e967bec6054a43efd464c4

DHY00500142506

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 30, 2005

Aug 30, 2025

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