ILIA IGG/IGM/igA negative quality solution solution - Taiwan Registration 50c3ab270416ad037a08704bbf31c962
Access comprehensive regulatory information for ILIA IGG/IGM/igA negative quality solution solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 50c3ab270416ad037a08704bbf31c962 and manufactured by PHADIA AB. The authorized representative in Taiwan is PHADIA TAIWAN INC..
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Device Details
Product Details
This product is used to monitor the performance of the Fadia 100, Fadia 200 and Fadia 250 instruments for in vitro determination of autologous antibodies.
A Clinical chemistry and clinical toxicology
A.1660 Quality control materials (analytical and non-analytical)
import
Dates and Status
Mar 18, 2015
Mar 18, 2030