Sanmeng corrected reference serum - Taiwan Registration 60370cc7ed8482dc1c2cfa70b8492980
Access comprehensive regulatory information for Sanmeng corrected reference serum in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 60370cc7ed8482dc1c2cfa70b8492980 and manufactured by FISHER DIAGNOSTICS, A DIVISION OF FISHER SCIENTIFIC COMPANY, LLC, A SUBSIDIARY OF THERMO FISHER. The authorized representative in Taiwan is BEAM INTERNATIONAL INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including THERMO ELECTRON CORPORATION, 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
This calibration serum is used on clinical chemistry analyzers as a secondary calibrator for general analysis
A Clinical chemistry and clinical toxicology
A.1150 Calibrated Products
import
Dates and Status
Dec 11, 2009
Dec 11, 2014
May 17, 2018
Cancellation Information
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