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Percutaneous nerve stimulator - Taiwan Registration 0af7bec1309e10fb80d961d5d2beb569

Access comprehensive regulatory information for Percutaneous nerve stimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0af7bec1309e10fb80d961d5d2beb569 and manufactured by WELL-LIFE HEALTHCARE LIMITED. The authorized representative in Taiwan is S&T BIOMED CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including BIO ELECTRONICS PTY LTD., AND GIKEN CO., LTD., and 2 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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0af7bec1309e10fb80d961d5d2beb569
Registration Details
Taiwan FDA Registration: 0af7bec1309e10fb80d961d5d2beb569
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Device Details

Percutaneous nerve stimulator
TW: ไธ–ๅปถ็ถ“็šฎ็ฅž็ถ“ๅˆบๆฟ€ๅ™จ
Risk Class 2
Cancelled

Registration Details

0af7bec1309e10fb80d961d5d2beb569

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

Contract manufacturing;; Domestic

Dates and Status

Nov 07, 2019

Jul 21, 2021

Jul 21, 2023

Cancellation Information

Logged out

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