Taiwan FDA registration e127a38e1ba6379fdd809ce95d608200

"DORNIER" extracorporeal shock wave lithotripsy

TW: “多尼爾”體外震波碎石機
Taiwan flagTaiwan·Risk Class 2·DORNIER MEDTECH SYSTEMS GMBH·Registered Jul 30, 2018 – Jul 30, 2028Active
Registration details
Analysis ID
e127a38e1ba6379fdd809ce95d608200
Customs Code
DHAS5603137402
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 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
Jul 30, 2018
Expiry Date
Jul 30, 2028
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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 e127a38e1ba6379fdd809ce95d608200 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 America, Inc.; 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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