Coronary ductus artery
- Analysis ID
- 3778f1ed60f8b818bc119136d3553677
- Customs Code
- DHA00600668203
- Manufacturer Country
- United States
- Authorized Representative
- LORION ENTERPRISES INC.
- Product Type (Level 1)
- 0601 Intensive Care Unit and Cardiac Intensive Care Unit Equipment
- Import Information
- import
- Registration Date
- Jun 30, 1992
- Expiry Date
- Jun 30, 1997
- Cancellation Date
- Oct 07, 1999
- Status
- Logged out
- Reason
- 未展延而逾期者;;改列無須辦理查驗之醫療器材
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Access comprehensive regulatory information for Coronary ductus artery in Taiwan's medical device market through Pure Global AI's free database. is registered under number 3778f1ed60f8b818bc119136d3553677 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, 1 companies making similar products including BOSTON SCIENTIFIC EUROPE SPRL, and 1 recent registrations in the same category. 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.