"Lifetech Technologies" Hertel ventricular septal defect occluder - Taiwan Registration 7bdbc696e46bfa78005a6fa2715643a7
Access comprehensive regulatory information for "Lifetech Technologies" Hertel ventricular septal defect occluder in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 7bdbc696e46bfa78005a6fa2715643a7 and manufactured by LIFETECH SCIENTIFIC (SHENZHEN) CO., LTD. The authorized representative in Taiwan is KAISEN MEDICAL 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.
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7bdbc696e46bfa78005a6fa2715643a7
Registration Details
Taiwan FDA Registration: 7bdbc696e46bfa78005a6fa2715643a7
Device Details
"Lifetech Technologies" Hertel ventricular septal defect occluder
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Risk Class 3

