"Fushi" bronchial tube blocker - Taiwan Registration 7def660d2e4c047d803cc4ea4a13aca9
Access comprehensive regulatory information for "Fushi" bronchial tube blocker in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7def660d2e4c047d803cc4ea4a13aca9 and manufactured by Fuji Systems Corporation, Shirakawa Plant. The authorized representative in Taiwan is BIOTRONIC INSTRUMENT ENTERPRISE 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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7def660d2e4c047d803cc4ea4a13aca9
Registration Details
Taiwan FDA Registration: 7def660d2e4c047d803cc4ea4a13aca9
Device Details
"Fushi" bronchial tube blocker
TW: โๅฏไธโๆฏๆฐฃ็ฎกๅ
ง็ฎก้ป้ๅจ
Risk Class 2

