Standard No.:	YY/T 1256-2024
English Name:	Ureaplasma nucleic acid detection kit
Chinese Name:	解脲脲原体核酸检测试剂盒
Chinese Classification:	C44    Medical laboratory equipment
Professional Classification:	YY    Professional Standard - Pharmaceutics
ICS Classification:	11.100.10 11.100.10    In vitro diagnostic test systems 11.100.10
Source Content Issued by:	National Medical Products Adminstration
Issued on:	2024-2-7
Implemented on:	2025-3-1
Status:	valid
Superseding:	YY/T 1256-2015 Ureaplasma nucleic acid amplification detection kit
Target Language:	English
File Format:	PDF
Word Count:	6500 words
Translation Price(USD):	195.0
Delivery:	via email in 1~3 business day

本文件规定了解脲脲原体核酸检测试剂盒的分类、技术要求、标签、使用说明书、包装、运输和贮存，描述了相应的试验方法。
本文件适用于检测人泌尿道、生殖道和呼吸道脲原体的核酸检测试剂盒，采用的方法学有荧光PCR法、恒温扩增法、PCR膜杂交法。