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"Irek" extracorporeal shock wave therapy device - Taiwan Registration 2d1ab6cdc68195a8403e16b2dc3028d9

Access comprehensive regulatory information for "Irek" extracorporeal shock wave therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 2d1ab6cdc68195a8403e16b2dc3028d9 and manufactured by E.M.S. Electro Medical Systems S.A.;; E.M.S. ELECTRO MEDICAL SYSTEMS S.A.. The authorized representative in Taiwan is MEDEN INTERNATIONAL INC..

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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2d1ab6cdc68195a8403e16b2dc3028d9
Registration Details
Taiwan FDA Registration: 2d1ab6cdc68195a8403e16b2dc3028d9
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Device Details

"Irek" extracorporeal shock wave therapy device
TW: โ€œไผŠ้›ทๅ…‹โ€้ซ”ๅค–้œ‡ๆณขๆฒป็™‚ๅ„€
Risk Class 3

Registration Details

2d1ab6cdc68195a8403e16b2dc3028d9

DHA00602444109

Company Information

Product Details

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

N Orthopedics

N.0001 ้ชจ็ง‘็”จ้ซ”ๅค–้œ‡ๆณข็ณป็ตฑ

import

Dates and Status

Jan 14, 2013

Jan 14, 2028