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“EMS” Primo Radial Shockwave - Taiwan Registration 8da2a88558dd6e6d58b3144e89aacd9d

Access comprehensive regulatory information for “EMS” Primo Radial Shockwave in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 8da2a88558dd6e6d58b3144e89aacd9d and manufactured by EMS PHYSIO LTD.. 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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8da2a88558dd6e6d58b3144e89aacd9d
Registration Details
Taiwan FDA Registration: 8da2a88558dd6e6d58b3144e89aacd9d
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Device Details

“EMS” Primo Radial Shockwave
TW: “伊美適” 震波治療儀
Risk Class 3
MD

Registration Details

8da2a88558dd6e6d58b3144e89aacd9d

Ministry of Health Medical Device Import No. 035845

DHA05603584501

Company Information

United Kingdom

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedics

N0001 Extracorporeal shock wave system for orthopedics

Imported from abroad

Dates and Status

Sep 08, 2022

Sep 08, 2027