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"DORNIER" extracorporeal shock wave lithotripsy - Taiwan Registration e127a38e1ba6379fdd809ce95d608200

Access comprehensive regulatory information for "DORNIER" extracorporeal shock wave lithotripsy in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e127a38e1ba6379fdd809ce95d608200 and manufactured by DORNIER MEDTECH SYSTEMS GMBH. The authorized representative in Taiwan is MEDEN INTERNATIONAL INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Dornier MedTech America, Inc.; DORNIER MEDTECH SYSTEMS GMBH, and 1 recent registrations in the same category. 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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e127a38e1ba6379fdd809ce95d608200
Registration Details
Taiwan FDA Registration: e127a38e1ba6379fdd809ce95d608200
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Device Details

"DORNIER" extracorporeal shock wave lithotripsy
TW: โ€œๅคšๅฐผ็ˆพโ€้ซ”ๅค–้œ‡ๆณข็ขŽ็ŸณๆฉŸ
Risk Class 2

Registration Details

e127a38e1ba6379fdd809ce95d608200

DHAS5603137402

Company Information

Germany

Product Details

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

H Gastroenterology and urology

H.5990 ้ซ”ๅค–้œ‡ๆณข็ขŽ็Ÿณๅ™จ

Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input

Dates and Status

Jul 30, 2018

Jul 30, 2028

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