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"Bifu" plasma separation sleeve - Taiwan Registration 47f0bf139091514297be65e098ff51a5

Access comprehensive regulatory information for "Bifu" plasma separation sleeve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 47f0bf139091514297be65e098ff51a5 and manufactured by Fresenius Kabi AG;; Fenwal International, Inc.. The authorized representative in Taiwan is Fresenius Kabi, Taiwan 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.

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47f0bf139091514297be65e098ff51a5
Registration Details
Taiwan FDA Registration: 47f0bf139091514297be65e098ff51a5
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Device Details

"Bifu" plasma separation sleeve
TW: "ๆฏ”ๅญš"่ก€ๆผฟๅˆ†้›ขๅฅ—
Risk Class 2

Registration Details

47f0bf139091514297be65e098ff51a5

DHA00601752205

Company Information

Dominican Republic;;Germany

Product Details

For details, it is Chinese approved copy of the imitation order

D Anesthesiology

D.5830 Instruments for automatic blood transfer

import

Dates and Status

Dec 19, 2006

Dec 19, 2026