"Asahi" does not need a guide tube for percutaneous coronary angioplasty - Taiwan Registration 983a9a63eca233790d89a2b4d3a445aa
Access comprehensive regulatory information for "Asahi" does not need a guide tube for percutaneous coronary angioplasty in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 983a9a63eca233790d89a2b4d3a445aa and manufactured by ASAHI INTECC CO., LTD. SETO FACTORY. 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.
Free Database
Powered by Pure Global AI
89,000+ Devices
983a9a63eca233790d89a2b4d3a445aa
Registration Details
Taiwan FDA Registration: 983a9a63eca233790d89a2b4d3a445aa
Device Details
"Asahi" does not need a guide tube for percutaneous coronary angioplasty
TW: โๆๆฅโ็ก้ๅฐๅผ้ๆฐดๆผพ็ถ็ฎๅ ็ๅ่ๆๅ่กๅฐๅผๅฐ็ฎก
Risk Class 2

