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.
Device Details
Registration Details
fe7105926354c9c2dfd87a043a51a9fb
DHY00500292505
Product Details
For details, it is Chinese approved copy of the imitation order
K Neuroscience
K.5890 Transcutaneous electrical nerve stimulator for pain relief
Domestic
Dates and Status
Apr 27, 2010
Aug 12, 2016
Apr 25, 2018
Cancellation Information
Logged out
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