"Kubota" Blood Bank Centrifuge for In Vitro Diagnostic Use (Non-Sterile) - Taiwan Registration 07ee47f278591de9b5dfd1f958adee1a
Access comprehensive regulatory information for "Kubota" Blood Bank Centrifuge for In Vitro Diagnostic Use (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 07ee47f278591de9b5dfd1f958adee1a and manufactured by KUBOTA MFG. CORP. FUJIOKA PLANT. The authorized representative in Taiwan is DOUBLE EAGLE ENTERPRISE CO., LTD..
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Device Details
Registration Details
07ee47f278591de9b5dfd1f958adee1a
Ministry of Health Medical Device Import Registration No. 019541
DHA08401954100
Product Details
Limited to the first level identification range of blood bank centrifuge (B.9275) for in vitro diagnostic of medical equipment management methods.
B Hematology and pathology devices
B9275 Blood bank centrifuge for in vitro diagnostics
Imported from abroad
Dates and Status
Oct 01, 2021
Oct 31, 2023