ILIA IGG Corrective Reagent Group - Taiwan Registration 2318664fec369bdedb2a54c4dacfdcd9
Access comprehensive regulatory information for ILIA IGG Corrective Reagent Group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2318664fec369bdedb2a54c4dacfdcd9 and manufactured by PHADIA AB. The authorized representative in Taiwan is PHADIA TAIWAN INC..
This page provides complete technical specifications, regulatory compliance details. 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
Performance changes (added applicable models): This product needs to be equipped with Fadia 100, Fadia 200 and Fadia 250 instruments, Ilia IgG correction solution/ILIA IgG correction sheet needs to use the microwell groove of the ILIA IgG correction to establish the IgG correction curve to analyze the patient specimen, and the ILIA IgG correction curve quality control fluid/the quality of the ILIA IgG correction curve quality control sheet needs to use the microwell groove for the use of the ILIA IgG correction curve to control the effectiveness of the IgG correction curve.
A Clinical chemistry and clinical toxicology
A.1150 Calibrated Products
import
Dates and Status
Mar 26, 2015
Mar 26, 2030

