Taiwan FDA registration 3d7412644a733ee0010b9633ce29d7a7

“Dornier” Extracorporeal shock wave therapy system

TW: “多尼爾”體外震波治療系統
Taiwan flagTaiwan·Risk Class 3·MD·DORNIER MEDTECH SYSTEMS GMBH·Registered Dec 09, 2016 – Dec 09, 2026Active
Registration details
Analysis ID
3d7412644a733ee0010b9633ce29d7a7
License Form
Ministry of Health Medical Device Import No. 029210
Customs Code
DHA05602921008
Company information
Manufacturer Country
Germany
Authorized Representative
MEDEN INTERNATIONAL INC.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
H Gastroenterology-urology devices
Import Information
Imported from abroad
Dates and status
Registration Date
Dec 09, 2016
Expiry Date
Dec 09, 2026
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About this record

Access comprehensive regulatory information for “Dornier” Extracorporeal shock wave therapy system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 3d7412644a733ee0010b9633ce29d7a7 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 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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