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Coronary ductus artery - Taiwan Registration 3778f1ed60f8b818bc119136d3553677

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.

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3778f1ed60f8b818bc119136d3553677
Registration Details
Taiwan FDA Registration: 3778f1ed60f8b818bc119136d3553677
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Device Details

Coronary ductus artery
TW: ๅ† ็‹€ๅ‹•่„ˆๅฐŽ็ฎก
Cancelled

Registration Details

3778f1ed60f8b818bc119136d3553677

DHA00600668203

Company Information

Product Details

0601 Intensive Care Unit and Cardiac Intensive Care Unit Equipment

import

Dates and Status

Jun 30, 1992

Jun 30, 1997

Oct 07, 1999

Cancellation Information

Logged out

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