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"Ouju" vector interference therapy instrument - Taiwan Registration 9875b3ac0da66da7a77c27127bd84ab0

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 9875b3ac0da66da7a77c27127bd84ab0 and manufactured by AND GIKEN 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 OG Wellness Technologies 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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9875b3ac0da66da7a77c27127bd84ab0
Registration Details
Taiwan FDA Registration: 9875b3ac0da66da7a77c27127bd84ab0
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Device Details

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

Registration Details

9875b3ac0da66da7a77c27127bd84ab0

DHA00601431600

Company Information

Product Details

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

o Physical Medical Sciences

import

Dates and Status

Apr 19, 2006

Apr 19, 2016

Jul 31, 2018

Cancellation Information

Logged out

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