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“STORZ MEDICAL” Modulith SLK Lithotripter - Taiwan Registration 08054058dfef6074fa6f1906bc73696d

Access comprehensive regulatory information for “STORZ MEDICAL” Modulith SLK Lithotripter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 08054058dfef6074fa6f1906bc73696d and manufactured by Storz Medical AG. The authorized representative in Taiwan is KINDMED CORPORATION.

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08054058dfef6074fa6f1906bc73696d
Registration Details
Taiwan FDA Registration: 08054058dfef6074fa6f1906bc73696d
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Device Details

“STORZ MEDICAL” Modulith SLK Lithotripter
TW: “斯拓茲”體外震波碎石機
Risk Class 2
MD

Registration Details

08054058dfef6074fa6f1906bc73696d

Ministry of Health Medical Device Import No. 032694

DHA05603269401

Company Information

Switzerland

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

Dates and Status

Jun 22, 2019

Jun 22, 2024