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“SANUWAVE” dermaPACE Therapeutic Shock Wave System - Taiwan Registration 82dee84e558cf5c6a937cc55453e27f5

Access comprehensive regulatory information for “SANUWAVE” dermaPACE Therapeutic Shock Wave System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 82dee84e558cf5c6a937cc55453e27f5 and manufactured by SANUWAVE, Inc.. The authorized representative in Taiwan is Rhythm Medical Ltd..

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82dee84e558cf5c6a937cc55453e27f5
Registration Details
Taiwan FDA Registration: 82dee84e558cf5c6a937cc55453e27f5
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Device Details

“SANUWAVE” dermaPACE Therapeutic Shock Wave System
TW: “索寧衛”得瑪貝司皮膚科震波治療系統
Risk Class 2
MD

Registration Details

82dee84e558cf5c6a937cc55453e27f5

Ministry of Health Medical Device Import No. 035942

DHA05603594209

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

I General, Plastic Surgery and Dermatology

I4685 Extracorporeal shock wave therapy equipment for chronic wounds

Imported from abroad

Dates and Status

Dec 06, 2022

Dec 06, 2027