YY/T 1233-2024 Active
YY/T 1233-2024 Cardiac troponin detection reagent kit(labelling immunoassay)
Abstract
This document specifies the requirements for myocardial troponin assay kits (labeled immunoassay), including identification, labeling, and user manuals, as well as packaging, transportation, and storage, and describes the corresponding test methods.
This document is applicable to kits used for the quantitative detection of myocardial troponin I (hereinafter referred to as cTnI) and myocardial troponin T (hereinafter referred to as cTnT) in human serum, plasma, or whole blood in vitro. The methods include enzyme-linked immunosorbent assay (ELISA), enzymatic and non-enzymatic chemiluminescence, electrochemiluminescence, and time-resolved fluorescence immunoassay, etc.
General Product Information
| Document Type | Industry standards-Medicine |
|---|---|
| Standard Status | Active |
| Standard Code | YY/T 1233-2024 |
| CCS | Medical laboratory equipment |
| Implement Date | 2025-10-15 |