Simplexa vzv swab direct package insert

Webb17 dec. 2024 · "With this release, we now offer a comprehensive menu of VZV and HSV tests from cerebrospinal fluid, mucocutaneous swab specimens, and cutaneous swab specimens," Michelle Tabb, chief scientific officer at DiaSorin Molecular, said in a statement. She said that customers can run all of the tests at the same time.

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WebbThe Simplexa™ VZV Direct assay is a real-time polymerase chain reaction (PCR) system that enables the direct amplificationand detection of VZV DNA from unprocessed … WebbSimplexa VZV Swab Direct, Simplexa VZV Positive Control Pack: DiaSorin Molecular LLC: K180559: HSV 1 & 2 ELITe MGB Kit; ELITe InGenius: ELITechGroup: K173798: Simplexa HSV 1 & 2 Direct, Simplexa HSV 1 & 2 Positive Control Pack: DiaSorin Molecular LLC: K162451: Solana HSV 1+2/VZV Assay: QUIDEL CORPORATION: K151906 circle of care round rock https://globalsecuritycontractors.com

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WebbThe Simplexa assays offer rapid and reliable alternatives for the detection of VZV in certain clinical specimens without the need for nucleic acid extraction. Keywords: cerebrospinal … WebbOur Simplexa TM HSV 1 & 2 Direct assay utilizes only 50 µl of sample and is cleared for BOTH CSF and mucocutaneous/cutaneous swabs. Broad coverage that includes … WebbThe Simplexa ® Congenital CMV Direct assay demonstrated high performance with excellent clinical agreement against a composite reference method consisting of PCR/bi … diamondback am2 lowest price

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Simplexa vzv swab direct package insert

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Webb7 jan. 2024 · Predicting Direct-Specimen SARS-CoV-2 Assay Performance Using Residual Patient Samples The Journal of Applied Laboratory Medicine Oxford Academic AbstractBackground. Diagnostic sensitivities of point-of-care SARS-CoV-2 assays depend on specimen type and population-specific viral loads. Evaluation of these Webb30 aug. 2024 · The DiaSorin Molecular Simplexa™ COVID-19 Direct assay system is a real-time RT-PCR system that en ables the direct amplification of Coronavirus SARS-CoV-2 RNA from nasopharyngeal swabs (NPS), nasal swabs (NS), nasal wash/aspirate (NW) or bronchoalveolar lavage (BAL) specimens.

Simplexa vzv swab direct package insert

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WebbOur Simplexa ® VZV Swab Direct assay utilizes only 50 µl of cutaneous or mucocutaneous swab specimen. Broad coverage includes samples collected from lesion locations … WebbThe DiaSorin Simplexa™ Varicella Zoster Virus (VZV) Direct FDA approved assay is a rapid real-time PCR that enables the direct amplification, detection of VZV from both cutaneous and mucocutaneous swab specimens and CSF specimens. A well conserved region of the VZV DNA polymerase gene is targeted to identify VZV in the specimen.

WebbDirect Amplification Disc. Simplexa ® Congenital CMV Direct Kit. The only FDA-cleared real-time PCR assay for the in vitro qualitative detection of cytomegalovirus (CMV) from both saliva swab and urine specimens … WebbThe Simplexa ® VZV Direct assay demonstrated high performance with excellent clinical agreement against PCR/bi-directional sequencing for both prospective and contrived …

WebbOur Simplexa ® HSV 1 & 2 Direct assay utilizes only 50 µl of sample and is cleared for BOTH CSF and mucocutaneous/cutaneous swabs. Broad coverage that includes samples collected from lesion locations … WebbSimplexa™VZV Swab Direct Kit Fast and Accurate VZV Testing A real-time PCR assay for the direct detection of varicella-zoster virus DNA from 50 μL of unprocessed cutaneous and mucocutaneous lesion swab specimens without nucleic acid extraction

WebbDEVICE: Simplexa™ VZV Swab Direct (20816101025712) Download: XML JSON Print Device Record History View all sections Close all sections Device Identifier (DI) …

Webb1 jan. 2024 · Nasal swabs directly tested on the ID NOW assay had 48% positive agreement compared to the CRS, whereas Simplexa had 88%, m2000 had 96% and Xpert had 100% positive agreement (Table 1a).While the deficit in positive percent agreement (PPA) seen in ID NOW test results is consistent with other early release studies in the scientific … circle of care wilton ctWebbassay, DiaSorin Molecular Simplexa™ VZV Swab Direct assay, and Quest Diagnostics Inc. laboratory developed test (LDT). Composite comparator analysis was used to determine the sensitivity and specificity of the Alinity m assay. Results: Alinity m assay sensitivity was 97.7% (85/87; 95% CI of 92.0% - 99.4%) and diamondback am2 reviewsWebbThe Simplexa HSV 1 & 2 Direct assay system is a real-time PCR that enables the direct amplification, detection and differentiation of HSV-1 and/or HSV-2 DNA from … diamondback am9WebbThe Simplexa® COVID-19 Direct has not been FDA cleared or approved. It has been authorized by FDA under an EUA for use by authorized laboratories. The test has been … diamondback andean 1WebbThe Simplexa™ HSV 1/2 & VZV Universal Direct assay demonstrated greater than 98% positive percent agreement and greater than or equal to 99.0% negative percent … diamondback am2 issuesWebbDEVICE: Simplexa™ VZV Swab Direct (20816101025712) Download: XML JSON Print Device Record History View all sections Close all sections Device Identifier (DI) Information Brand Name: Simplexa™ VZV Swab Direct Version or Model: MOL3655 Commercial Distribution Status: In Commercial Distribution Catalog Number: Company … diamondback aluminum truck bed coversWebbOur Simplexa ™ VZV Swab Direct assay utilizes only 50 µl of cutaneous or mucocutaneous swab specimen. Broad coverage includes samples collected from lesion locations … circle of centers