Pure Global

“Dornier” Extracorporeal shock wave therapy system - Taiwan Registration 3d7412644a733ee0010b9633ce29d7a7

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
1 Competitors
1 Recent Registrations
3d7412644a733ee0010b9633ce29d7a7
Registration Details
Taiwan FDA Registration: 3d7412644a733ee0010b9633ce29d7a7
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Dornier” Extracorporeal shock wave therapy system
TW: “多尼爾”體外震波治療系統
Risk Class 3
MD

Registration Details

3d7412644a733ee0010b9633ce29d7a7

Ministry of Health Medical Device Import No. 029210

DHA05602921008

Company Information

Germany

Product Details

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

H Gastroenterology-urology devices

Imported from abroad

Dates and Status

Dec 09, 2016

Dec 09, 2026

Companies Making Similar Products
Top companies providing products similar to "“Dornier” Extracorporeal shock wave therapy system"