Taiwan FDA registration 2f3ae26febc4195d5c2d82cdd3748c7e
“Spectranetics” Stellarex Drug-Coated Angioplasty Balloon
TW: “史特勞斯”司特樂塗藥球囊導管
Taiwan·Risk Class 2·MD·Spectranetics Corporation·Registered Jul 02, 2020 – Jul 02, 2025ExpiredRegistration details
- Analysis ID
- 2f3ae26febc4195d5c2d82cdd3748c7e
- License Form
- Ministry of Health Medical Device Import No. 033806
- Customs Code
- DHA05603380604
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
- Jul 02, 2020
- Expiry Date
- Jul 02, 2025
About this record
Access comprehensive regulatory information for “Spectranetics” Stellarex Drug-Coated Angioplasty Balloon in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2f3ae26febc4195d5c2d82cdd3748c7e and manufactured by Spectranetics Corporation. The authorized representative in Taiwan is LORION ENTERPRISES INC..
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