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"Noxon" Otien electromyography system - Taiwan Registration 3570365ad1943e9964045ee5048a301a

Access comprehensive regulatory information for "Noxon" Otien electromyography system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3570365ad1943e9964045ee5048a301a and manufactured by NORAXON USA, INC.. The authorized representative in Taiwan is AMPLE MEDICAL INSTRUMENTS 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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3570365ad1943e9964045ee5048a301a
Registration Details
Taiwan FDA Registration: 3570365ad1943e9964045ee5048a301a
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Device Details

"Noxon" Otien electromyography system
TW: โ€œ่ซพๅ…‹ๆฃฎโ€ๆญๆๆฉ่‚Œ้›ปๅœ–็ณป็ตฑ
Risk Class 2

Registration Details

3570365ad1943e9964045ee5048a301a

DHA05603371300

Company Information

United States

Product Details

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

K Neuroscience;;O Physical Medical Sciences

K.5050 ็”Ÿ็†่ฟด้ฅ‹ๅ„€;; O.1375 ่จบๆ–ท็”จ่‚Œ้›ปๅœ–ๅ„€

import

Dates and Status

Jun 09, 2020

Jun 09, 2025