Taiwan FDA registration 9ee22fd2fe2a85b8efe8915dc2721a72
"Boston Tech" Polaris defibrillation electrode catheter
TW: "波士頓科技" 北極星除顫電極導管
Registration details
- Analysis ID
- 9ee22fd2fe2a85b8efe8915dc2721a72
- Customs Code
- DHA00600999500
Company information
- Manufacturer
- BOSTON SCIENTIFIC CORPORTAION-SAN JOSE
- Manufacturer Country
- United States
- Authorized Representative
- KINGDOM EAST ENTERPRISE CO., LTD.
Product details
- Intended Use
- Vacuum.
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Import Information
- import
Dates and status
- Registration Date
- Jul 23, 2002
- Expiry Date
- Jul 23, 2007
- Cancellation Date
- Nov 16, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Boston Tech" Polaris defibrillation electrode catheter in Taiwan's medical device market through Pure Global AI's free database. is registered under number 9ee22fd2fe2a85b8efe8915dc2721a72 and manufactured by BOSTON SCIENTIFIC CORPORTAION-SAN JOSE. The authorized representative in Taiwan is KINGDOM EAST ENTERPRISE CO., LTD..
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.
Free DatabasePowered by Pure Global AI89,000+ Devices