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"Ouju" vector interference therapy instrument - Taiwan Registration 5cd24fa4db95ddbd436218f3ebf12ea2

Access comprehensive regulatory information for "Ouju" vector interference therapy instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5cd24fa4db95ddbd436218f3ebf12ea2 and manufactured by OG Wellness Technologies Co., Ltd. Oku Factory. The authorized representative in Taiwan is AMPLE MEDICAL INSTRUMENTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including AND GIKEN CO., LTD., OKU 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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5cd24fa4db95ddbd436218f3ebf12ea2
Registration Details
Taiwan FDA Registration: 5cd24fa4db95ddbd436218f3ebf12ea2
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Device Details

"Ouju" vector interference therapy instrument
TW: โ€œๆญๅฑ…โ€ๅ‘้‡ๅนฒๆ“พๆฒป็™‚ๅ„€
Risk Class 2
Cancelled

Registration Details

5cd24fa4db95ddbd436218f3ebf12ea2

DHA00602102506

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

o Physical Medical Sciences

O.5850 5850.

import

Dates and Status

May 13, 2010

May 13, 2020

May 19, 2022

Cancellation Information

Logged out

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