Taiwan FDA registration f10470393c07b9e06140c93848dd9e69
Coronary angioplasty system
TW: 冠狀動脈血管整形系統
Registration details
- Analysis ID
- f10470393c07b9e06140c93848dd9e69
- Customs Code
- DHA00600835409
Company information
- Manufacturer Country
- United States
- Authorized Representative
- LORION ENTERPRISES INC.
Product details
- Intended Use
- The details are as detailed as the approved version of the imitation single label.
- Product Type (Level 1)
- 0699 Other Intensive Care Unit & Cardiac Care Unit Equipment
- Import Information
- import
Dates and status
- Registration Date
- Aug 12, 1997
- Expiry Date
- Aug 12, 2002
- Cancellation Date
- Sep 11, 1998
Cancellation information
- Status
- Logged out
- Reason
- 移轉(申請商)
About this record
Access comprehensive regulatory information for Coronary angioplasty system in Taiwan's medical device market through Pure Global AI's free database. is registered under number f10470393c07b9e06140c93848dd9e69 and manufactured by BOSTON SCIENTIFIC CORPORATION (MANSFIELD FACILITY). The authorized representative in Taiwan is LORION ENTERPRISES INC..
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