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Funai Biomedical Low Frequency Therapy Device - Taiwan Registration fe7105926354c9c2dfd87a043a51a9fb

Access comprehensive regulatory information for Funai Biomedical Low Frequency 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 fe7105926354c9c2dfd87a043a51a9fb and manufactured by Hongtai Enterprise Co., Ltd. Rende Factory. The authorized representative in Taiwan is Hongtai Enterprise Co., Ltd. Rende Factory.

This page provides complete technical specifications, regulatory compliance details. 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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fe7105926354c9c2dfd87a043a51a9fb
Registration Details
Taiwan FDA Registration: fe7105926354c9c2dfd87a043a51a9fb
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Device Details

Funai Biomedical Low Frequency Therapy Device
TW: ่ˆนไบ•็”Ÿ้†ซไฝŽ้€ฑๆณขๆฒป็™‚ๅ™จ
Risk Class 2
Cancelled

Registration Details

fe7105926354c9c2dfd87a043a51a9fb

DHY00500292505

Company Information

Taiwan, Province of China

Product Details

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

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Dates and Status

Apr 27, 2010

Aug 12, 2016

Apr 25, 2018

Cancellation Information

Logged out

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