"Carneka" coronary angioplasty probes the catheter - Taiwan Registration 793241a8532940dea2cf45da6b35d18d
Access comprehensive regulatory information for "Carneka" coronary angioplasty probes the catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 793241a8532940dea2cf45da6b35d18d and manufactured by KANEKA MEDIX CORPORATION KANAGAWA PLANT. The authorized representative in Taiwan is QUALTECH CONSULTING CORPORATION.
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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793241a8532940dea2cf45da6b35d18d
Registration Details
Taiwan FDA Registration: 793241a8532940dea2cf45da6b35d18d
Device Details
"Carneka" coronary angioplasty probes the catheter
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Risk Class 2

