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“Zimmer” GentlePro Shock Wave Therapy System - Taiwan Registration 9e689adb461fee69a1ab26501819896a

Access comprehensive regulatory information for “Zimmer” GentlePro Shock Wave Therapy System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 9e689adb461fee69a1ab26501819896a and manufactured by ZIMMER MEDIZINSYSTEME GMBH. The authorized representative in Taiwan is WOH MEDICAL 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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9e689adb461fee69a1ab26501819896a
Registration Details
Taiwan FDA Registration: 9e689adb461fee69a1ab26501819896a
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Device Details

“Zimmer” GentlePro Shock Wave Therapy System
TW: “利麥爾”傑特普體外震波治療儀
Risk Class 3
MD

Registration Details

9e689adb461fee69a1ab26501819896a

Ministry of Health Medical Device Import No. 034580

DHA05603458009

Company Information

Germany

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedic devices

N0001 Extracorporeal shock wave system for orthopedics

Imported from abroad

Dates and Status

Jun 03, 2021

Jun 03, 2026