Pure Global

“Storz Medical” Masterpuls Shock Wave Therapy System and Accessories - Taiwan Registration 25a6f5247e725aa1b2b0f5075f9bdbda

Access comprehensive regulatory information for “Storz Medical” Masterpuls 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 25a6f5247e725aa1b2b0f5075f9bdbda and manufactured by Storz Medical AG. The authorized representative in Taiwan is KINDMED CORPORATION.

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
25a6f5247e725aa1b2b0f5075f9bdbda
Registration Details
Taiwan FDA Registration: 25a6f5247e725aa1b2b0f5075f9bdbda
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Storz Medical” Masterpuls Shock Wave Therapy System and Accessories
TW: “斯拓茲”麥斯波震波治療系統
Risk Class 3
MD

Registration Details

25a6f5247e725aa1b2b0f5075f9bdbda

Ministry of Health Medical Device Import No. 031100

DHA05603110006

Company Information

Switzerland

Product Details

For details, it is Chinese approved copy of the imitation order

N Orthopedic devices

N0001 Extracorporeal shock wave system for orthopedics

Imported from abroad

Dates and Status

May 28, 2018

May 28, 2028