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cobas®Liat®PCR系统

快速、简便、可靠、准确

cobas®Liat®系统

我们把实验室放进试管里

SARS-CoV-21、SARS-CoV-2和A/B型流感1A/B型流感和RSV型流感,A组链球菌和艰难梭菌2 *


当迫切需要诊断和治疗决定时,患者依靠您和您的工作人员提供反应最灵敏、最值得信赖的医疗服务。

cobasLiat PCR系统可用于检测和鉴定SARS-CoV-21、SARS-CoV-2和A/B型流感1A/B型流感和RSV型流感,A组链球菌和艰难梭菌2-在您自己的诊所,使用以前只有在复杂分子实验室才能使用的金标准PCR技术。

cobasLiat PCR系统体积小,易于使用,快速,可在患者预约结束时提供准确的结果。

cobasLiat系统是现场分子检测,您可以依赖。为了那些依赖你的病人。

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指尖

诊断测试无与伦比的准确性

……现在在医生的指尖

罗氏率先发展了聚合酶链反应(PCR)分析技术,现已被公认为实验室诊断的金标准。

  • 专利技术,获得诺贝尔奖
  • 通过复制从患者样本中提取的DNA或RNA来识别传染病
  • 检测的高灵敏度和特异性降低了假阴性和假阳性的风险

被公认为20世纪最重要的科学进步之一1在美国,聚合酶链反应(PCR)是一种快速、简单的方法,可以从一条原始链中复制出无限份DNA或RNA。

1.Mark R. Hughes,美国国立卫生研究院国家人类基因组研究中心(或许更广为人知的名字是人类基因组计划)副主任。

cobas Liat PCR系统用于结果导向的患者护理

在大分子实验室中,PCR分析可以同时对许多样品进行,这是一个需要熟练技术人员的多步骤过程。

cobasLiat系统完全自动化这些步骤,用于单个样品的快速分析,使其成为对时间敏感的办公室诊断的理想选择。

不需要操作员干预或解释。

  • 每一个cobasLiat检测管包含一套化学试剂,用于检测特定传染病特有的DNA或RNA序列
  • cobasLiat分析仪,压力和热量精确地应用于管段,混合样品和试剂在规定的顺序
  • 样本中的DNA或RNA被放大和分析,以检测和识别疾病
  • 在20分钟或更短的时间内生成准确的阳性或阴性结果
结果
参考文献
  1. 本产品尚未获得FDA的许可或批准,但已根据EUA获得FDA的授权。
  2. 本产品已获FDA批准,可由CLIA认证的授权实验室使用,以执行中等复杂性测试。

概述

订购信息

技术文件

技术规格

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技术规格

电力供应
输入 100-240V AC /50-60Hz
输出 15v dc / 8.6a
环境要求(运行)
温度 +15°C至+32°C
相对湿度 15% ~ 80%(不凝结)
最大高度 海拔2000米(6500英尺)
尺寸和重量
高度 19.0厘米(7.5“)
宽度 11.4厘米(4.5英寸)
长度 24.1厘米(9.5英寸)
重量 3.76公斤(8.3磅)
数据和显示
最多可存储、备份和存档20,000条记录
启用HL7的连接
支持的条码类型
Codabar
39码
代码93
代码128
EAN-8
EAN -13
GS1-DataBar
5个中的2个交叉
订购信息
cobas®Liat分析仪 07341920190
cobas®SARS CoV-21 09211101190
cobas®SARS CoV-2 & A/B流感1 09408592190
cobas®A型链球菌 07341911190
cobas流感A/B和RSV 08160104190
cobas®C.艰难梭菌2 07454945190
参考文献
  1. 本产品尚未获得FDA的许可或批准,但已根据EUA获得FDA的授权。
  2. 本产品已获FDA批准,可由CLIA认证的授权实验室使用,以执行中等复杂性测试。
分析菜单

在罗氏分子诊断的长期承诺下,cobas Liat系统可以帮助您应对对时间敏感的患者护理需求。

SARS-CoV-21

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SARS-CoV-21

用于筛查有症状和无症状患者

SARS-CoV-21分析性能
积极的协议 消极的协议 LoD
有症状的个体 96.1% 96.8% 2.4 x 10-2TCID50/毫升
(24拷贝/毫升)
无症状的个体 100% 98.9% 1.2 × 10-2TCID50/毫升
的cobas®SARS-CoV-2核酸检测用于cobas®Liat®系统(cobas®SARS-CoV-2)是一种自动实时RT-PCR检测方法,用于快速体外定性检测SARS-CoV-2的核酸,检测方法包括自行收集的前鼻(鼻)拭子(在医疗保健机构根据医疗保健提供者的指示收集)和医疗保健提供者从其医疗保健提供者或任何个人收集的疑似COVID-19的个人的鼻咽、中鼻甲和前鼻(鼻)拭子,包括没有症状或其他原因怀疑COVID-19的个人。包插入包插入cobas®Liat®SARS-CoV-2。

SARS-CoV-2 & A/B流感1

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SARS-CoV-2 & A/B流感1

适用于有症状和无症状患者

SARS-CoV-2 & A/B流感1分析性能
积极的协议 消极的协议 LoD
“非典” 100% 100% 1 × 10-2TCID50/毫升
(12拷贝/毫升)
流感了 98.4% 96.5% 2 × 103- 2 * 10-2TCID50/毫升
流感B 97.9% 99.4% 2 × 103- 4 * 103TCID50/毫升
的cobas®SARS-CoV-2和A/B流感病毒核酸检测用于cobas®Liat®系统(cobas®SARS-CoV-2和A/B型流感病毒)是一种自动多重实时RT - PCR检测方法,旨在同时在体外快速定性检测和区分SARS-CoV-2、A型流感病毒和B型流感病毒RNA,检测样本包括医疗保健提供者收集的鼻咽拭子和自收集的鼻拭子(在医疗保健提供者的指导下从医疗保健提供者怀疑感染COVID-19的呼吸道病毒的个人收集的鼻拭子)。SARS-CoV-2与流感引起的呼吸道病毒感染的临床体征和症状可能相似。包插入cobas®Liat®SARS-CoV-2 & A/B流感。

喉炎的症状一

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喉炎的症状一

准确的结果,不需要确认

cobas®链球菌A化验性能
灵敏度 特异性 LoD
98.3% 94.2% 5 - 20 CFU /毫升
cobas链球菌A具有高敏感性,在处方抗生素治疗时提供了所需的保证。FDA 510(k)通过并放弃CLIA。用于cobas®链球菌A1眼镜蛇®链球菌一种用于cobas Liat系统(cobas®Liat Strep A)是一种定性体外诊断试验,用于检测化脓性链球菌(A组β-溶血性链球菌,Strep A),从有咽炎症状和体征的患者的咽拭子标本。的cobas®Liat Strep A法利用核酸纯化和聚合酶链反应(PCR)技术,通过靶向化脓性链球菌基因组的一段来检测化脓性链球菌。1.包插入cobas®链球菌A, Rev. 4, 07806124190-02EN。

流感A/B和RSV

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流感A/B和RSV

1个样品,1个测试,3个结果,0个年龄限制

cobas流感A/B和RSV检测性能
积极的协议 消极的协议
甲型流感 98.3% 96.0%
乙型流感 95.2% 99.4%
RSV * 97.0% 98.7%
*与fda批准的基于实验室的多重实时逆转录PCR (RT-PCR)检测相比;cobas®甲型/乙型流感及呼吸道合胞病毒[包装说明书]。cobas流感A/B和RSV具有非凡的敏感性,在处方抗病毒治疗时提供了所需的保证。FDA 510(k)通过并放弃CLIA。用于cobas®A/B型流感和RSV1型®cobas使用的A/B型流感和RSV核酸检测®Liat®系统(cobas®流感病毒A/B & RSV)是一种自动多重实时RT-PCR检测方法,用于在具有呼吸道感染体征和症状的患者鼻咽拭子标本中,结合临床和流行病学危险因素,对甲型流感病毒、乙型流感病毒和呼吸道合胞病毒(RSV) RNA进行体外快速定性检测和鉴别。该测试旨在用于人类甲型流感、乙型流感和RSV的鉴别诊断,而不是用于检测丙型流感。包插入cobas®甲型/乙型流感及呼吸道合胞病毒,Rev. 1

梭状芽孢杆菌2

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梭状芽孢杆菌2

准确的结果,不需要确认

梭状芽孢杆菌2分析性能
敏感vs.直接培养 特异性与文化 LoD
94.6% 96.2% 90 CFU /拭子
的cobas®Cdiff用于cobas的核酸检测®Liat®该系统是一种自动化的体外定性诊断测试,使用实时聚合酶链反应(PCR)在怀疑患有艰难梭菌感染(CDI)的患者的未成形(液体或软质)粪便标本中检测产毒艰难梭菌(C. difficile)的毒素B (tcdB)基因。的cobas®Cdiff用于cobas的核酸检测®Liat®该系统旨在与临床和流行病学危险因素相结合,用于辅助人类CDI的诊断。包插入cobas®Liat®梭状芽孢杆菌。
参考文献
  1. 本产品尚未获得FDA的许可或批准,但已根据EUA获得FDA的授权。
  2. 本产品已获FDA批准,可由CLIA认证的授权实验室使用,以执行中等复杂性测试。
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