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"Funai" low week wave therapy device - Taiwan Registration de9f8b12305df4cceb61d4b6fea94316

Access comprehensive regulatory information for "Funai" low week wave 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 de9f8b12305df4cceb61d4b6fea94316 and manufactured by Hongtai Enterprise Co., Ltd. Rende Factory. The authorized representative in Taiwan is HOME CARE TECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Hongtai Enterprise Co., Ltd. Rende 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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de9f8b12305df4cceb61d4b6fea94316
Registration Details
Taiwan FDA Registration: de9f8b12305df4cceb61d4b6fea94316
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Device Details

"Funai" low week wave therapy device
TW: "่ˆนไบ•" ไฝŽ้€ฑๆณขๆฒป็™‚ๅ™จ
Risk Class 2
Cancelled

Registration Details

de9f8b12305df4cceb61d4b6fea94316

DHY00500101602

Company Information

Taiwan, Province of China

Product Details

K Neuroscience

Domestic

Dates and Status

Aug 15, 2003

Aug 12, 2016

Apr 25, 2018

Cancellation Information

Logged out

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