Taiwan FDA registration 78f90982f1115c0102106f09a46ddab2

"DORNIER" extracorporeal shock wave lithotripsy

TW: “多尼爾”體外震波碎石機
Taiwan flagTaiwan·Risk Class 2·Dornier MedTech America, Inc.; DORNIER MEDTECH SYSTEMS GMBH·Registered Dec 13, 2016 – Dec 13, 2026Active
Registration details
Analysis ID
78f90982f1115c0102106f09a46ddab2
Customs Code
DHAS5602921207
Company information
Manufacturer Country
United States;;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 and urology
Product Type (Level 2)
H.5990 體外震波碎石器
Import Information
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
Registration Date
Dec 13, 2016
Expiry Date
Dec 13, 2026
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About this record

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..

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