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“Spectranetics” AngioSculpt PTA Scoring Balloon Catheter - Taiwan Registration 718adf3749abb84140fee44d1704122f

Access comprehensive regulatory information for “Spectranetics” AngioSculpt PTA Scoring Balloon Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 718adf3749abb84140fee44d1704122f and manufactured by Spectranetics Corporation. The authorized representative in Taiwan is LORION ENTERPRISES INC..

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718adf3749abb84140fee44d1704122f
Registration Details
Taiwan FDA Registration: 718adf3749abb84140fee44d1704122f
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Device Details

“Spectranetics” AngioSculpt PTA Scoring Balloon Catheter
TW: “史特勞斯”安卓史考特週邊血管網狀氣球導管
Risk Class 2
MD

Registration Details

718adf3749abb84140fee44d1704122f

Ministry of Health Medical Device Import No. 029432

DHA05602943200

Company Information

United States

Product Details

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

E Cardiovascular devices

E1250 Percutaneous catheter

Imported from abroad

Dates and Status

Feb 23, 2017

Feb 23, 2027