YY/T 1162-2009 Translated English of Chinese Standard. (YYT 1162-2009, YY/T1162-2009, YYT1162-2009): Alpha-fetoprotein quantitative detection reagent (kit) (Chemiluminescent immunoassay)https://www.chinesestandard.net, 08/12/2014 - 13 من الصفحات This standard specifies the terms and definitions, classification, requirements, test methods, inspection rules, identification, labels, instructions, packaging, transportation and storage of alpha-fetoprotein quantitative detection reagent (kit) (chemiluminescence immunoassay). This standard is applicable to the quantitative detection of the alpha-fetoprotein quantitative detection reagent (kit) in the human blood matrix or other body fluid components, based on the principle of chemiluminescence immunoassay. It includes the enzymatic and non-enzymatic chemiluminescence immunoassay detection reagent (kit) in carriers of micro-plates, tubes, magnetic particles, micro-beads and plastic beads. This standard is not applicable to the requirements of calibrators and quality control products in the kit. |
المحتوى
3 | |
Scope | 4 |
Classification | 6 |
Test methods | 7 |
Inspection rules of products | 9 |
Marks labels and instructions | 11 |
Packaging transportation and storage | 12 |
13 | |
عبارات ومصطلحات مألوفة
10-times measurement results According to different Alpha-fetoprotein AFP alpha-fetoprotein quantitative detection batch of reagent Beijing blood matrix Calculate the mean chemical reaction chemiluminescence immunoassay reagent Coefficient of variation component of reagent detect the accuracy detection reagent kit device registration certificate documents so quoted ex-factory inspection following contents formula GB/T inspection items inspection quantity instrument-automatic operation IU/mL allowable variation least the following linear range M+2SD mean value measurement procedure Medical device registration methods of 6.3 micro-beads and plastic Minimum detectable concentration minimum detection limit non-enzymatic chemiluminescence immunoassay Number of medical Packaging perform the detection period of validity photon Product batch number Product name qualified quantitative detection reagent quantity and retained-sample reagent kits registration certificate number reinspection requirements of 5.3 requirements of 5.8 result shall comply retained-sample quantity Sampling quantity serum sample Shanghai standard deviation SD terms and definitions Traceability The manufacturer type inspection variation CV vitro diagnostic Within-batch difference zero-concentration calibrator