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"DORNIER" extracorporeal shock wave lithotripsy - Taiwan Registration 78f90982f1115c0102106f09a46ddab2

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 78f90982f1115c0102106f09a46ddab2 and manufactured by Dornier MedTech America, Inc.; 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 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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78f90982f1115c0102106f09a46ddab2
Registration Details
Taiwan FDA Registration: 78f90982f1115c0102106f09a46ddab2
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Device Details

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

Registration Details

78f90982f1115c0102106f09a46ddab2

DHAS5602921207

Company Information

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

Dec 13, 2016

Dec 13, 2026

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