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Lycra low-frequency therapy device - Taiwan Registration 856f8b36814855f60cc9831278dc5df3

Access comprehensive regulatory information for Lycra 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 856f8b36814855f60cc9831278dc5df3 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. 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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856f8b36814855f60cc9831278dc5df3
Registration Details
Taiwan FDA Registration: 856f8b36814855f60cc9831278dc5df3
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Device Details

Lycra low-frequency therapy device
TW: ่ŠๅกไฝŽ้€ฑๆณขๆฒป็™‚ๅ™จ
Risk Class 2
Cancelled

Registration Details

856f8b36814855f60cc9831278dc5df3

DHY00500144805

Company Information

Taiwan, Province of China

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

Sep 14, 2005

Aug 12, 2006

Nov 27, 2012

Cancellation Information

Logged out

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