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“Storz Medical” MASTERPULS ONE Shock Wave Therapy System - Taiwan Registration 3e58604c53a5b73b201e9023eb82e94d

Access comprehensive regulatory information for “Storz Medical” MASTERPULS ONE 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 3e58604c53a5b73b201e9023eb82e94d and manufactured by Storz Medical AG. The authorized representative in Taiwan is KINDMED CORPORATION.

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3e58604c53a5b73b201e9023eb82e94d
Registration Details
Taiwan FDA Registration: 3e58604c53a5b73b201e9023eb82e94d
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Device Details

“Storz Medical” MASTERPULS ONE Shock Wave Therapy System
TW: “斯拓茲”麥斯波萬震波治療系統
Risk Class 3
MD

Registration Details

3e58604c53a5b73b201e9023eb82e94d

Ministry of Health Medical Device Import No. 035943

DHA05603594301

Company Information

Switzerland

Product Details

-肩關節慢性鈣化性或非鈣化性肌腱炎 (Chronic tendinitis of the shoulder)-慢性筋肌膜炎疼痛 (Chronic myofascial pain)-慢性足底筋膜炎 (Chronic plantar fasciitis)-慢性肘外上髁炎 (Chronic lateral epicondylitis)

N Orthopedics

N0001 Extracorporeal shock wave system for orthopedics

Imported from abroad

Dates and Status

Dec 07, 2022

Dec 07, 2027