"Dulac" blood bank centrifuge for in vitro diagnostics (unsterilized) - Taiwan Registration 282e713729bc221baa4bd5ac5b4bd225
Access comprehensive regulatory information for "Dulac" blood bank centrifuge for in vitro diagnostics (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 282e713729bc221baa4bd5ac5b4bd225 and manufactured by PRINTER DIAGNOSTICS. The authorized representative in Taiwan is SYNERGY BIOMEDICAL LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including PRINTER DIAGNOSTICS, 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 classification and grading management method of medical equipment, in vitro diagnostic blood bank centrifuge (B.9275) first level identification range.
B Hematology, pathology, and genetics
B.9275 Blood bank centrifuge for in vitro diagnostics
QMS/QSD;; ่ผธๅ ฅ
Dates and Status
Oct 01, 2021
Oct 31, 2025