release time:2021-07-26 15:11:59
Common in vitro diagnostic devices:
According to the detection category, it can be divided into blood test, biochemical diagnosis, immunodiagnosis, molecular diagnosis, microbiological diagnosis, POCT, etc.
The FDA classifies medical devices (including IVD products) into Class I, Class II, or Class III based on the level of regulatory control required to reasonably ensure safety and effectiveness. The classification of IVD (or other medical devices) determines the appropriate pre-marketing process.
2022-03-10
Azotemia is an increase in the concentration of urea and creatinine and other non-protein-derived nitrogenous wastes in the blood due to impaired excretion of nitrogenous wastes by the kidneys, resulting in azotemia in pets.
2021-11-08
1)Add a sample volume of 100 μl to the reagent tray, with a permissible sample range of 90-120 μl (it is recommended that a blood volume of at least 250 μl be collected for review).2) The use of lithium heparin anticoagulation tubes is recommended for sample processing.
2021-08-19
Chemiluminescence immunoassay is an analytical method that determines the content of a substance based on the intensity of the radiation light produced by a chemical reaction.