"TERUMO" CAPIOX ARTERIAL FILTER - Taiwan Registration 3f60ef069759702563afea6915186f5a
Access comprehensive regulatory information for "TERUMO" CAPIOX ARTERIAL FILTER in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3f60ef069759702563afea6915186f5a and manufactured by ASHITAKA FACTORY OF TERUMO CORPORATION. The authorized representative in Taiwan is TERUMO TAIWAN MEDICAL CO., LTD..
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3f60ef069759702563afea6915186f5a
Registration Details
Taiwan FDA Registration: 3f60ef069759702563afea6915186f5a
Device Details
"TERUMO" CAPIOX ARTERIAL FILTER
TW: ๅ่้ๆฟพๅจ
Risk Class 2
MD

