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“SONOLITH I-move” Extracorporeal Lithotripter - Taiwan Registration 6b5500c7ddd5044c1afc6a544f6259a7

Access comprehensive regulatory information for “SONOLITH I-move” Extracorporeal Lithotripter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6b5500c7ddd5044c1afc6a544f6259a7 and manufactured by EDAP TMS FRANCE. The authorized representative in Taiwan is LITHO MED TRADING CO., LTD..

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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6b5500c7ddd5044c1afc6a544f6259a7
Registration Details
Taiwan FDA Registration: 6b5500c7ddd5044c1afc6a544f6259a7
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Device Details

“SONOLITH I-move” Extracorporeal Lithotripter
TW: “蘇諾里仕 艾莫孚”體外震波碎石機
Risk Class 2
MD

Registration Details

6b5500c7ddd5044c1afc6a544f6259a7

Department of Health Medical Device Import No. 022988

DHA00602298806

Company Information

France

Product Details

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

H Gastroenterology-urology devices

H5990 Extracorporeal shock wave lithotripsy

Imported from abroad; The use of this equipment shall comply with the "Administrative Measures for the Implementation or Use of Specific Medical Technical Examination and Inspection Medical Equipment"

Dates and Status

Nov 04, 2011

Nov 04, 2026