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"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
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Device Details

"TERUMO" CAPIOX ARTERIAL FILTER
TW: ๅ‹•่„ˆ้Žๆฟพๅ™จ
Risk Class 2
MD

Registration Details

3f60ef069759702563afea6915186f5a

Department of Health Medical Device Import No. 008337

DHA00600833709

Company Information

Product Details

๏ผŽ

1310 Transfusion Filter

Imported from abroad

Dates and Status

Jul 22, 1997

Feb 09, 2024