Taiwan FDA registration 3f1b8d623c3b4b07bfe6be912e371a07

“Dornier” Extracorporeal shock wave therapy system

TW: “多尼爾”骨震波治療儀
Taiwan flagTaiwan·Risk Class 3·MD·DORNIER MEDTECH SYSTEMS GMBH·Registered Sep 23, 2014 – Sep 23, 2024Expired
Registration details
Analysis ID
3f1b8d623c3b4b07bfe6be912e371a07
License Form
Ministry of Health Medical Device Import No. 026617
Customs Code
DHA05602661700
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)
N Orthopedic devices
Product Type (Level 2)
N0001 Extracorporeal shock wave system for orthopedics
Import Information
Imported from abroad
Dates and status
Registration Date
Sep 23, 2014
Expiry Date
Sep 23, 2024
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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 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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