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Quidel

开发,制造和市场在关注传染病和生殖健康方面的临时诊断测试(POC)(POC)
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临床实验室

呼吸病毒面板
Savanna RVP4 Assay

Savanna RVP4分析(呼吸道病毒面板4)是一种快速的,多重的实时PCR测试从具有呼吸道感染体征和症状的患者获得的培养基中,呼吸合胞病毒(RSV)和SARS-COV-2 RNA从人鼻或鼻咽拭子中分离出来。Savanna RVP4分析由独立的单使用测定法组成,不需要样品或试剂准备,然后将墨盒插入Savanna仪器。所有样品和试剂制剂,核酸提取和扩增以及病毒RNA的实时检测均在大约22分钟内完全自动化并完成。
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COVID-19 Rapid Antibody Test
CoronaCHEK Rapid Antibody Convenience Kit

The CoronaCHEK COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) is a rapid chromatographic immunoassay for the qualitative detection of IgG and IgM antibodies to SARS-CoV-2 in human whole blood, serum, or plasma. The FDA EUA authorized and CLIA waived kit comes with one procedure card, one package insert, two fact sheets, and 20 individually packaged devices. Each package includes one test cassette, one dropper, one lancet, one single-use buffer, and one alcohol wipe.
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COVID-19 IgG/IgM快速测试
Ecotest Covid-19 IgG/IgM快速测试设备

Ecotest COVID-19 IgG/IgM快速测试装置是一种快速的侧向气流色谱免疫测定法,用于在人类静脉全血(钠EDTA),血清,血浆(血浆)(质量)中的IgM和IgG抗体的定性检测和分化SARS-COV-2的定性检测和分化。EDTA钠)和指尖全血。Ecotest COVID-19 IgG/IgM快速测试装置旨在用作识别对SARS-COV-2具有适应性免疫反应的个体,表明最近或事先感染。目前,感染后多长时间抗体持续多长时间,并且抗体的存在是否赋予保护性免疫,这是尚不清楚的。
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COVID-19快速测试盒
promistigncovid-19-Rapid Test Cassette

The RightSignCOVID-19 Rapid Test Cassette is a rapid lateral flow chromatographic immunoassay intended for the qualitative detection and differentiation of IgM and IgG antibodies to SARS-CoV-2 in human venous whole blood (sodium heparin, potassium EDTA, and sodium citrate), serum or plasma (sodium heparin, potassium EDTA and sodium citrate), and fingerstick whole blood. The test is intended for use as an aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating recent or prior infection.
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SARS-COV-2抗原测试
QuickVue SARS抗原测试

The QuickVue SARS Antigen Test detects SARS-CoV-2 antigens directly from anterior nares swab specimens. The test provides accurate and reliable results in 10 minutes, allowing for testing of patients suspected of COVID-19/2019-nCoV in near-patient testing environments.
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SARS-CoV-2 Assay
SOLANA SARS-COV-2分析

The Solana SARS-CoV-2 Assay is an isothermal Reverse Transcriptase - Helicase-Dependent Amplification (RT-HDA) assay intended for the qualitative detection of nucleic acid from SARS-CoV-2 in nasopharyngeal (NP) and nasal (NS) swab specimens from individuals suspected of COVID-19 by their healthcare provider. The assay consists of two major steps: (1) specimen preparation, and (2) amplification and detection of target sequences specific to SARS-CoV-2 using isothermal Reverse Transcriptase - Helicase-Dependent Amplification (RT-HDA) in the presence of target-specific fluorescence probes which is performed in the Solana instrument. Results are displayed on the touchscreen, can be saved to the instrument, printed, and are capable of being sent to the LIS and exported through one of Solana’s five USB ports.
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流感 + SARS抗原测试
Sofia 2 Flu + SARS Antigen FIA

索非亚2流感 + SARS抗原荧光免疫测定法(FIA)在夹层设计中使用先进的基于免疫荧光的侧向流技术,以定性检测流感和流感B和流感B和SARS-COV-2的核素蛋白。索非亚2流感 + SARS抗原FIA带有Sofia 2分析仪在15分钟内提供自动化和客观的结果,从而可以测试涉嫌在护理点的患者,涉嫌流感,流感B和COVID-19/2019-NCOV。
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SARS-CoV-2 Assay
Lyra Sars-Cov-2分析

Lyra SARS-COV-2分析是一种实时RT-PCR测定法Covid-19。授权测试包括在生物素核酸核酸核酸酯系统或EMAG系统上提取核酸,然后在六个热环生物上进行RT-PCR。
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SARS抗原荧光免疫测定
索非亚SARS抗原荧光免疫测定(FIA)

Sofia SARS抗原荧光免疫测定(FIA)在三明治设计中使用先进的基于免疫荧光的侧向流技术,用于从SARS-COV-2中定性检测核素蛋白。Sofia Sars抗原FIA配备了Sofia 2和Sofia分析仪,可在15分钟内提供自动化和客观的结果,从而在接近患者的测试环境中测试涉嫌COVID-19/2019-NCOV的患者。
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SARS-CoV-2 Assay
Lyra Direct SARS-COV-2分析

Lyra Direct SARS-COV-2分析是一种实时RT-PCR测定法COVID-19的症状。该测定目标是SARS-COV-2病毒的非结构性多蛋白(PP1AB),并具有一步试剂设置和三步样品准备,并在不到70分钟的时间内可用测试结果。
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Newsof QUIDEL

Quidel Signs Definitive Agreement to Acquire Ortho Clinical Diagnostics

24 Dec 2021
Quidel Signs Definitive Agreement to Acquire Ortho Clinical Diagnostics
Quidel Corporation (San Diego, CA, USA) and Ortho Clinical Diagnostics (Raritan, NJ, USA) have entered into a definitive agreement in which Quidel will acquire Ortho, one of the world’s largest in vitro diagnostics companies.
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Quidel Receives Amended FDA Emergency Use Authorization for New AI-Powered Sofia Q Rapid Antigen Test Device

2021年6月15日
Quidel Receives Amended FDA Emergency Use Authorization for New AI-Powered Sofia Q Rapid Antigen Test Device
Quidel Corporation (San Diego, CA, USA) has received an amended Emergency Use Authorization (EUA) from the US Food and Drug Administration (FDA) allowing the company to market Sofia Q, its latest addition to the Sofia and Sofia 2 line of Fluorescent Immunoassay Analyzers (FIA).
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Quidel to Acquire Alere Triage Assets

2017年7月24日
Quidel to Acquire Alere Triage Assets
Quidel Corporation, a provider of rapid diagnostic testing solutions, cellular-based virology assays and molecular diagnostic systems, has entered into definitive agreements to acquire the Triage MeterPro cardiovascular (CV) and toxicology assets (“Triage business”) and the B-type Naturietic Peptide (BNP) assay business run on Beckman Coulter analyzers (“BNP business”) from Alere Inc. These products are being divested in order to obtain antitrust approvals required for Abbott’s pending acquisition of Alere.
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关于Quidel

Number of Employees:400-999
Year of Establishment:1979
开发,制造和市场在关注传染病和生殖健康方面的临时诊断测试(POC)(POC)
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免疫测试

免疫测试

模型: 索非亚链球菌A+ FIA
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描述:

Sofia链球菌A+ FIA使用先进的基于免疫荧光的侧向流技术来检测有症状患者喉咙拭子的A组链球菌抗原。它为真正快速的链球菌测试提供了五分钟结果的快速时间,并使用了干净,易于使用和处置的独立测试盒。

标签:[[临床实验室],[[快速测试这是给予的
Features 规格

Features

•在5分钟内导致
•独立的测试盒
• Fixed-volume pipette
• Objective result
•套件中包含的所有组件
• Room temperature storageRequest Information

规格

•样品类型的喉咙拭子
• Time to results 5 minutes
•套件存储条件室温(15°C至30°C / 59°F至86°F)
•控制正和负面
• Sensitivity* 93.7%
• Specificity* 94.4%
• Shelf life 24 months from date of manufacture
•CLIA复杂性免除Request Information

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