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"DORNIER" extracorporeal shock wave lithotripter - Taiwan Registration f22ed1d6a07e3823731efbd457bf7875

Access comprehensive regulatory information for "DORNIER" extracorporeal shock wave lithotripter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f22ed1d6a07e3823731efbd457bf7875 and manufactured by Dornier MedTech America, Inc.; DORNIER MEDTECH SYSTEMS GMBH. The authorized representative in Taiwan is MEDEN INTERNATIONAL INC..

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f22ed1d6a07e3823731efbd457bf7875
Registration Details
Taiwan FDA Registration: f22ed1d6a07e3823731efbd457bf7875
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Device Details

"DORNIER" extracorporeal shock wave lithotripter
TW: "ๅคšๅฐผ็ˆพ "้ซ”ๅค–้œ‡ๆณข็ขŽ็ŸณๆฉŸ
Risk Class 2

Registration Details

f22ed1d6a07e3823731efbd457bf7875

DHAS0600725905

Company Information

Product Details

vacuum

H Gastroenterology and urology

H.5990 ้ซ”ๅค–้œ‡ๆณข็ขŽ็Ÿณๅ™จ

Input;; Contract manufacturing

Dates and Status

Jul 26, 1994

Feb 09, 2029