"Beckman Coulter" hemocytometry diluted sheath fluid (non-sterile) - Taiwan Registration e9614ab951449c842f8c5b3d1d6b469c
Access comprehensive regulatory information for "Beckman Coulter" hemocytometry diluted sheath fluid (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 e9614ab951449c842f8c5b3d1d6b469c and manufactured by BECKMAN COULTER GmbH. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Beckman Coulter Inc., 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
It is limited to the first level of identification of "blood cell thinners (B.8200)" in the management measures for the classification and grading of medical devices.
B Hematology, pathology, and genetics
B.8200 Hemocytodilant
Input;; QMS/QSD
Dates and Status
Aug 28, 2024
Aug 28, 2029