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"Kabi" blood bag tube sealer (unsterilized) - Taiwan Registration c5a898279fdda9973b64bd8d0a321cca

Access comprehensive regulatory information for "Kabi" blood bag tube sealer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c5a898279fdda9973b64bd8d0a321cca and manufactured by Fresenius Kabi AG; Fresenius HemoCare GmbH. The authorized representative in Taiwan is FRESENIUS KABI TAIWAN LIMITED.

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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c5a898279fdda9973b64bd8d0a321cca
Registration Details
Taiwan FDA Registration: c5a898279fdda9973b64bd8d0a321cca
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Device Details

"Kabi" blood bag tube sealer (unsterilized)
TW: โ€œๅกๆฏ”โ€ ่ก€่ข‹็ฎกๅฐๅฃๆฉŸ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

c5a898279fdda9973b64bd8d0a321cca

DHA09401351603

Company Information

Product Details

Limited to the classification and grading management measures for medical equipment "Heating and Sealing Equipment (B.9750)" first level identification range.

B Hematology, pathology, and genetics

B.9750 Heat-sealing equipment

import

Dates and Status

Oct 21, 2013

Oct 21, 2028