"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.
Device Details
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

