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“Dornier” Extracorporeal shock wave therapy system - Taiwan Registration 3f1b8d623c3b4b07bfe6be912e371a07

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 3f1b8d623c3b4b07bfe6be912e371a07 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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3f1b8d623c3b4b07bfe6be912e371a07
Registration Details
Taiwan FDA Registration: 3f1b8d623c3b4b07bfe6be912e371a07
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Device Details

“Dornier” Extracorporeal shock wave therapy system
TW: “多尼爾”骨震波治療儀
Risk Class 3
MD

Registration Details

3f1b8d623c3b4b07bfe6be912e371a07

Ministry of Health Medical Device Import No. 026617

DHA05602661700

Company Information

Germany

Product Details

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

N Orthopedic devices

N0001 Extracorporeal shock wave system for orthopedics

Imported from abroad

Dates and Status

Sep 23, 2014

Sep 23, 2024

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