"Xuanjiang" in vitro diagnostic blood bank intelligent decapping centrifuge (unsterilized) - Taiwan Registration 0b47a06423c4e17c1010c63119bfa678
Access comprehensive regulatory information for "Xuanjiang" in vitro diagnostic blood bank intelligent decapping centrifuge (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0b47a06423c4e17c1010c63119bfa678 and manufactured by LANNER BIOTECHNOLOGY CO., LTD.. The authorized representative in Taiwan is LANNER BIOTECHNOLOGY CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including LANNER BIOTECHNOLOGY CO., LTD., and 1 recent registrations in the same category. 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 first level identification range of blood bank centrifuge (B.9275) for in vitro diagnostic of medical equipment management methods.
B Hematology, pathology, and genetics
B.9275 Blood bank centrifuge for in vitro diagnostics
ๅ็ข;; QMS/QSD
Dates and Status
Feb 03, 2016
Feb 03, 2026
Sep 30, 2021
Cancellation Information
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