"Bantron" glass fiber reinforced coronary polymer - Taiwan Registration 97d9febef510dbe4803ffacd6c6d5ace
Access comprehensive regulatory information for "Bantron" glass fiber reinforced coronary polymer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 97d9febef510dbe4803ffacd6c6d5ace and manufactured by PENTRON CLINICAL. The authorized representative in Taiwan is MONITEX INDUSTRIAL 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.
Free Database
Powered by Pure Global AI
89,000+ Devices
97d9febef510dbe4803ffacd6c6d5ace
Registration Details
Taiwan FDA Registration: 97d9febef510dbe4803ffacd6c6d5ace
Device Details
"Bantron" glass fiber reinforced coronary polymer
TW: "็ญ็นๆ" ็ป็็บ็ถญๅผทๅๅ ๅฟ่ๅๆ
Risk Class 2

