"Sturz" extracorporeal shock wave therapy instrument - Taiwan Registration 48d0fec6ebd9748eaf7f4f4a67dc747b
Access comprehensive regulatory information for "Sturz" extracorporeal shock wave therapy instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 48d0fec6ebd9748eaf7f4f4a67dc747b 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.
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48d0fec6ebd9748eaf7f4f4a67dc747b
Registration Details
Taiwan FDA Registration: 48d0fec6ebd9748eaf7f4f4a67dc747b
Device Details
"Sturz" extracorporeal shock wave therapy instrument
TW: โๆฏ็น่ฒโ้ซๅค้ๆณขๆฒป็ๅ
Risk Class 2

