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“Storz” Duolith Shock Wave Therapy System and Accessories - Taiwan Registration cde22ab3ac16682012aef5c97ed7bf42

Access comprehensive regulatory information for “Storz” Duolith Shock Wave Therapy System and Accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number cde22ab3ac16682012aef5c97ed7bf42 and manufactured by STORZ MEDICAL AG. The authorized representative in Taiwan is SHAWHAN BIOMEDICAL CO., LTD..

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cde22ab3ac16682012aef5c97ed7bf42
Registration Details
Taiwan FDA Registration: cde22ab3ac16682012aef5c97ed7bf42
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Device Details

“Storz” Duolith Shock Wave Therapy System and Accessories
TW: “思拓”多力震波治療系統與配件
Risk Class 3
MD
Cancelled

Registration Details

cde22ab3ac16682012aef5c97ed7bf42

Ministry of Health Medical Device Import No. 026804

DHA05602680409

Company Information

Switzerland

Product Details

N Orthopedic devices

N0001 Extracorporeal shock wave system for orthopedics

Imported from abroad

Dates and Status

Dec 03, 2014

Dec 03, 2019

Aug 05, 2022

Cancellation Information

Logged out

未展延而逾期者