"Belsen" Kema coronary stent system - Taiwan Registration 7727c9dacb469f3f4b564422270f03ea
Access comprehensive regulatory information for "Belsen" Kema coronary stent system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 7727c9dacb469f3f4b564422270f03ea and manufactured by BIOSENSORS EUROPE SA;; BIOSENSORS INTERVENTIONAL TECHNOLOGIES PTE LTD.. The authorized representative in Taiwan is K&C 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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7727c9dacb469f3f4b564422270f03ea
Registration Details
Taiwan FDA Registration: 7727c9dacb469f3f4b564422270f03ea
Device Details
"Belsen" Kema coronary stent system
TW: โ็พ็พๆฃฎโๅ
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Risk Class 3

