Taiwan FDA registration 718adf3749abb84140fee44d1704122f
“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
Taiwan·Risk Class 2·MD·Spectranetics Corporation·Registered Feb 23, 2017 – Feb 23, 2027ActiveRegistration details
- Analysis ID
- 718adf3749abb84140fee44d1704122f
- License Form
- Ministry of Health Medical Device Import No. 029432
- Customs Code
- DHA05602943200
Company information
- Manufacturer
- Spectranetics Corporation
- Manufacturer Country
- United States
- Authorized Representative
- LORION ENTERPRISES INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1250 Percutaneous catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 23, 2017
- Expiry Date
- Feb 23, 2027
About this record
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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