"Hannitec" de-leukocyte blood processing filtration system - Taiwan Registration 9ca4e21df8ccd6a313e7e6a1c88b2a94
Access comprehensive regulatory information for "Hannitec" de-leukocyte blood processing filtration system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9ca4e21df8ccd6a313e7e6a1c88b2a94 and manufactured by Haemonetics Manufacturing, Inc.. The authorized representative in Taiwan is HAEMONETICS ASIA INCORPORATED TAIWAN BRANCH (U.S.A.).
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Device Details
Product Details
For details, it is Chinese approved copy of the imitation order
B Hematology, pathology, and genetics
B.9100 Containers for the collection and disposal of blood and blood components
import
Dates and Status
Jul 16, 2012
Jul 16, 2022
Apr 12, 2024
Cancellation Information
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