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Medical card low frequency therapy device - Taiwan Registration 6602f51d3ba099191198b9004a4f4b3c

Access comprehensive regulatory information for Medical card 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 6602f51d3ba099191198b9004a4f4b3c 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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6602f51d3ba099191198b9004a4f4b3c
Registration Details
Taiwan FDA Registration: 6602f51d3ba099191198b9004a4f4b3c
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Device Details

Medical card low frequency therapy device
TW: ้†ซๅกไฝŽ้€ฑๆณขๆฒป็™‚ๅ™จ
Risk Class 2

Registration Details

6602f51d3ba099191198b9004a4f4b3c

DHY00500331509

Company Information

Taiwan, Province of China

Product Details

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

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K.5890 Transcutaneous electrical nerve stimulator for pain relief

Contract manufacturing;; Domestic

Dates and Status

May 16, 2011

May 16, 2026