Taiwan FDA registration 4fc1da5feefdd7b707cf05d6049580e8
“Boston Scientific” AngioJet Ultra Power Pulse Kit
TW: “波士頓科技”安傑特液體脈衝注射組
Taiwan·Risk Class 2·MD·BOSTON SCIENTIFIC CORPORATION·Registered Oct 19, 2016 – Oct 19, 2026ActiveRegistration details
- Analysis ID
- 4fc1da5feefdd7b707cf05d6049580e8
- License Form
- Ministry of Health Medical Device Import No. 028870
- Customs Code
- DHA05602887006
Company information
- Manufacturer
- BOSTON SCIENTIFIC CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- Dutch Boston Technology Co., Ltd. Taiwan Branch
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)
- E1210 Continuous Irrigation Catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 19, 2016
- Expiry Date
- Oct 19, 2026
About this record
Access comprehensive regulatory information for “Boston Scientific” AngioJet Ultra Power Pulse Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4fc1da5feefdd7b707cf05d6049580e8 and manufactured by BOSTON SCIENTIFIC CORPORATION. The authorized representative in Taiwan is Dutch Boston Technology Co., Ltd. Taiwan Branch.
This page provides complete technical specifications, regulatory compliance details. 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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