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Archive for category: Product News

Product News

C403 Bio Rad

Anti-Mullerian Hormone control

, 26 August 2020/in Product News /by 3wmedia

Bio-Rad has expanded its portfolio of quality control products for reproductive health and prenatal testing with the launch of Liquichek AMH Control. This product is a dedicated Anti-Mullerian Hormone (AMH) control designed to meet the increasing demand for a liquid, independent, assayed quality control used primarily in fertility/In Vitro Fertilization (IVF) clinics. 
AMH is emerging as an important fertility marker used by healthcare professionals and fertility specialists as an indicator of ovarian reserve. The test result provides an assessment of the available egg supply and consequently, remaining fertility window.  Females with higher AMH values may have a better response to ovarian stimulation for IVF and egg retrieval. The accurate assessment of AMH can provide a clinician with valuable insight used to manage an individual’s reproductive health.
Liquichek AMH Control is offered as a single analyte with three clinically relevant levels for monitoring the precision of AMH assays.  
Bio-Rad’s Liquichek AMH Control addresses needs in the fertility and reproductive health testing market, especially when offered as part of a broad range of fertility controls including Lyphochek Fertility Control, Liquichek Maternal Serum II, and Liquichek Maternal 1st Trimester.

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C382 EKF

Glycated albumin assay kit

, 26 August 2020/in Product News /by 3wmedia

Now available is a new Stanbio Chemistry Glycated Albumin (GA) assay kit. 
GA is a sensitive marker for intermediate glycemic control in diabetes and can fill the gap between long-term and short-term measurements of blood glucose status. This is particularly useful just after the start or during an alteration in diabetes treatment, where measurement of GA can confirm blood glucose changes over just 2 to 3 weeks. It is also useful for prognosis in hemodialysis patients and during pregnancy when HbA1c may provide an insufficient indication of glycemic levels. The Stanbio Chemistry GA assay uses an enzymatic method with liquid reagents and requires no preparation. It can be used on compatible open channel clinical chemistry analysers and expresses results as a ratio of Glycated Albumin to Albumin in mmol/mol from a small amount of blood serum. GA accurately reflects the latest blood glucose status as it is found throughout the body and is a type of protein that can readily be glycated.

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Programmable pump

, 26 August 2020/in Product News /by 3wmedia

The Intelligent Programmable Pump from Fluid Metering, Inc. combines FMI’s precision valveless STH Stepper Pump with integral programmable driver in a compact design ideal for integration with OEM instrumentation. The driver provides precision servo control of the STH pumps stepper motor for resonance-free, quite operation. Having 5 programmable inputs and 2 outputs, the Intelligent Pump is compatible with multiple programming platforms including Visual Basic, C/C++, Delphi, LabView. Analog 0-5 VDC, RS-232, and CANopen protocol are supported with an optional EtherCAT communication module available.
The programmable driver and stepper provide precision control of FMI’s CeramPump integral valveless piston pump. FMI’s CeramPump technology features only one moving part, a sapphire-hard ceramic piston, in contact with fluid. The rotating and reciprocating piston accomplishes both the pumping and valving functions effectively eliminating check valves present in conventional reciprocating piston and diaphragm pump designs.  

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C396 Sebia copy crop

Capillary electrophoresis analyser now connected to lab automation system

, 26 August 2020/in Product News /by 3wmedia

Sebia’s latest generation instrument, Capillarys 3 TERA, is now connectable to the Inpeco automation systems, available under the FlexLab brand name and as Aptio by Siemens. This analyser offers a large menu of tests for the diagnosis and follow-up of myeloma, diabetes and hemoglobin disorders. Two assays are now connectable to Inpeco automation: HbA1c and Serum Protein Electrophoresis. Other tests such as Serum Immunotyping and Hemoglobin electrophoresis will follow soon.
The Capillarys 3 TERA TLA connection with FlexLab opens new opportunities for lab automation and brings the capillary electrophoresis analyser closer to the core clinical laboratory workflow. Designed as a point-of-space connection, Capillarys 3 TERA TLA can process serum and whole blood at the same time thanks to a specific development on FlexLab.
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C345 Sclavo IMG 0112 cut

Specific proteins tests for urine samples

, 26 August 2020/in Product News /by 3wmedia

Urine testing provides unique information pertaining to a multiple series of renal and extra-renal diseases.
Based on immunoturbidimetric technology, a new line of specific proteins urinary tests from Sclavo Diagnostics uses liquid, ready-to-use reagents in various packaging formats. It includes:
Bence Jones Proteinuria, which provides measurement of free and bound K and λ light chains in liquid chemistry and may be useful in the overall evaluation of tubular damages;
(Micro) Albuminuria, a strong marker of glomerular damages, is a most valuable indication for diabetes, arterial hypertension and gravidic gestosis, in addition to renal diseases; ∝-1-Microglobulin and β-2-Microglobulin efficiently detect any tubular damages and their increased level can additionally help identifying Bence Jones Proteinuria; Immunoglobulins G in urine helps the diagnosis, in the presence of albuminuria, of all forms of primary and advanced secondary glomerular disease; Transferrin is useful in pathologies such as renal failure, especially in case of glomerular deficiencies: by assaying urinary albumin and transferrin, it is possible to gain information on electric charge selectivity since both proteins have similar sizes but a different charge.
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PRODUCT BECKMAN COULTER

Beckman Coulter’s SARS-CoV-2 IgG antibody test now available in markets accepting CE Mark

, 26 August 2020/in Product News /by 3wmedia

Beckman Coulter’s Access SARS-CoV-2 IgG assay is now available in markets accepting the CE Mark, the company said in statement 15 June. It has already shipped tests to more than 400 hospitals, clinics and diagnostics laboratories in the United States and has begun shipping to customers globally. Beckman Coulter has more than 16,000 immunoassay analysers worldwide and has increased manufacturing to deliver more than 30 million tests a month.
Many of Beckman Coulter’s analysers can deliver up to 400 routine tests an hour. The Access SARS-CoV-2 IgG test can also be run on Beckman Coulter’s Access 2 analyser, a compact table-top analyser enabling high-quality serology testing to be carried out in small hospitals and clinics.
The Access SARS-CoV-2 IgG Assay is a qualitative immunoassay that detects IgG antibodies directed to the receptor-binding domain of the spike protein of the novel coronavirus that is driving the ongoing global pandemic. It is believed that these antibodies have the potential to be neutralizing antibodies and may play a role in lasting immunity. The test has a confirmed 99.8% specificity and 100% sensitivity at 18 days post PCR confirmed positive test. The assay uses immobilized virus antigens on magnetic particles to capture IgG antibodies from patient serum or plasma samples and reveals them using labelled anti-IgG antibodies.
Commenting on the assay, Shamiram R. Feinglass, M.D., MPH, Chief Medical Officer, Beckman Coulter, said: “An IgG antibody assay such as the test Beckman Coulter has developed can provide valuable information regarding community levels of immunity that will inform public health decision making and rollout of a vaccine when one does become available. The very high sensitivity and specificity of this assay provides a high positive predictive value, even when the overall incidence of disease is low. Additionally, since our assay can be run on multiple different types of analysers, it can be adapted to a variety of healthcare settings to best meet the needs of each community.”
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AD CLI MOLBIO DIAGNOSTICS 1

Molecular diagnostics platform for fast and point-of-care disease diagnosis

, 26 August 2020/in Corona News, Product News /by 3wmedia

Molecular diagnostics is known to have superior advantages for routine detection of infectious diseases and now has a very prominent place in clinical laboratories. Based on the principle of DNA/RNA amplification, molecular diagnostic techniques help in early diagnosis of infectious diseases, providing the added edge of excellent sensitivity and specificity. However, this technique has, thus far, been limited to centralized laboratories due to dependency on complex and expensive infrastructure, highly skilled manpower, special storage conditions and a need for batch testing. This results in high turn-around time and poses major logistics challenges, such as sample degradation, contamination, report delays, etc.
Molbio Diagnostics Pvt Ltd has developed and commercialized Truelab™, a commercial point-of-care (POC) molecular diagnostics platform that uses PCR technology with Truenat test chips. Truenat™ disease-specific test chips are available for the diagnosis of 22 infectious diseases (such as TB, H1N1, dengue, HIV, hepatitis, etc) and an additional 43 diseases (such as coronavirus, MERS, etc) are in the pipeline.
The Truelab™ platform, a global first, is a compact, battery-operated system, with single testing capability and provides sample-toresult times within 1 hour. Hence, it enables same-day reporting and initiation of evidencebased treatment for the patient. Doctors benefit from this technology by having a definitive diagnosis, early in the infection cycle, without patients/samples having to travel extensively to centralized facilities.
The Truenat™ assay is rapid and affordable with minimal infrastructure requirements. Thus, placing the Truelab™ multi-disease detection system in the most remote settings will enable mass access to advanced molecular testing for people of all socio-economic backgrounds, across the globe. The device has real-time data transfer capability (through SMS/email) for immediate reporting of results in emergency cases. Additionally, a cloud-based centralized data monitoring and surveillance network can be created and linked to all devices in a region. Complete data from tests performed can be accessed, analysed and recorded in real time. Such same-day reporting of results will strengthen the healthcare systems across countries by improving effectiveness of providing treatment and quarantining of patients, thus controlling spread of communicable diseases. The device is ideal for places that do not get regular electricity, and will work well even in primary healthcare centres, unlike other devices that require uninterrupted power supply, elaborate infrastructure and air-conditioning.
Molbio’s technology has been approved by the Indian Council of Medical Research in 2018, after 3 years of validation study across various sites in India. Internationally, the World Health Organization (WHO), after conducting a multicountry study, has released a rapid communication in January 2020 endorsing Truenat™ as an initial diagnostic test of Mycobacterium tuberculosis (MTB) and MTB-RIF (MTB rifampicin resistance) in view of its high diagnostic accuracy. The WHO has further endorsed Truenat™ for diagnosis of TB as a replacement of the less sensitive sputum smear microscopy. The performance of Truenat™ shows comparable accuracy with other WHO approved tests such as Genexpert, TB-LAMP® and line probe assay. Truenat™ will help in decentralizing and democratizing access to high quality diagnostics to millions of patients suffering from TB and other infectious diseases even at peripheral and remote settings.
At present, Truelab™ devices are installed in over 500 private laboratories, 350 government primary health centres in India and in 27 countries around the globe, extending across the continents of Asia, Africa, Europe and South America. WHO endorsement will further enable the product to be commercialized across more than 150 countries.
Truelab™ is patented across over 100 countries which enables the transition from presumptive to efficient, real-time and precise diagnosis of multiple diseases at reasonable price even in primary healthcare centres and smaller diagnostics labs, which can now deliver high-end molecular diagnostic tests.
Molbio Diagnostics is driven by the urgent need to provide world-class medical devices to enable better medicine through precise, faster, cost effective diagnosis and envisions to be a leading global player in the POC diagnostics segment by continuing to innovate and bring new technologies for social betterment.
In addition, given the current coronavirus pandemic, Molbio is pleased to announce that the Truenat™ Beta-CoV POC RT-PCR test is currently being validated through a regulatory process and is expected to be commercially available in the next couple of weeks. This rapid, portable, POC solution will enable molecular testing for COVID-19 to be performed even at the community level and will provide results within 1 hour from sampling.
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C448 BD COR 2018 Straight large

Automated molecular diagnostic system

, 26 August 2020/in Product News /by 3wmedia

The BD COR System from BD (Beckton, Dickinson and Company) is an automated, high throughput molecular diagnostics system developed for large capacity laboratories. The modular and scalable design addresses lab needs to expand molecular testing offerings and increase test volumes by integrating and automating the complete molecular laboratory workflow. The system allows samples to be processed directly from liquid-based cytology vials and is capable of running the diagnostic workflow from pre-analytical processing to test result, unlike other automated molecular diagnostic platforms. As offerings expand, the system will provide a solution for a menu of clinically differentiated diagnostic assays for infectious diseases.  It has on-board capacity for reagents and samples to provide up to 360 results in eight hours of system processing, eliminating multiple technologist interactions per shift. Currently, the BD COR System is CE-IVD marked. It integrates and automates the complete molecular laboratory workflow from pre-analytical processing to diagnostic test result. The system will be initially available with the BD Onclarity HPV Assay for the detection and extended genotyping of human papilloma virus (HPV). The system enables the processing of samples directly from liquid-based cytology vials, the creation of molecular aliquot tubes and assay testing, replacing labour-intensive and error-prone manual processes with automated ones. Over the coming years, the company plans to continue seeking regulatory authorizations to sell the BD COR System around the world while expanding the content menu to include many other assays for infectious diseases. The BD Onclarity HPV assay detects and identifies 14 high-risk human papillomavirus (HPV) types and provides genotyping information from specimens collected for cervical cancer screening purposes in the BD SurePath Vial and in the Hologic PreservCyt Solution (not approved in the United States). Different configurations of the test are CE marked and FDA approved.
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PRODUCT SIEMENS 1

INNOVANCE reagents support management of COVID-19 patients

, 26 August 2020/in Corona News, Product News /by 3wmedia

Siemens Healthineers’s INNOVANCE assays help improve efficiencies, workflow and resource management following a COVID-19 diagnosis.
In hospitalised COVID-19 patients, elevated D-dimer levels have been found to be strongly associated with disease severity and even mortality reflecting the procoagulant status and high thrombotic risk observed in many COVID-19 patients. Therefore, the monitoring of D-dimer levels is recommended for hospitalised COVID-19 patients to stratify their thrombotic risk including testing for deep vein thrombosis and pulmonary embolism and guiding treatment over the course of the disease.
Treating COVID-19 patients with anticoagulants has been associated with improved outcomes, both in and out of the intensive care unit setting.
Accurate antithrombin measurement in COVID-19 patients undergoing anticoagulant treatment may be useful to determine the efficacy of anticoagulant therapy as antithrombin levels might be reduced.
Siemens Healthineers has a comprehensive portfolio of assays for detection and monitoring of coagulation disorders.
For more information, visit: https://www.siemenshealthineers.com/hemostasis/ innovance-reagents-for-coagulation-disorders
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Greiner VACUETTE glucose FC

Sample tube with glucose stabilization immediately after collection

, 26 August 2020/in Product News /by 3wmedia

The VACUETTE FC Mix Tube is specifically designed for reliable detection of diabetes and taking appropriate measures to combat the condition. The citrate/citric acid buffer ensures a quick stabilization of the blood sample. The glycolysis is catalysed and suppressed. Therefore, the blood sugar is held constantly at the in vivo value. Due to the sodium fluoride additive contained in the VACUETTE FC Mix Tube, inhibition is extended to 48 hours. Additionally, Na2-EDTA is included as an anticoagulant, which is effective due to complexation of Ca++. The almost full inhibition of glycolysis in the VACUETTE FC Mix Tube means that diagnosis is a much more reliable process than before. The stabilization is carried out in whole blood and therefore does not require immediate centrifugation. Unlike in tubes with liquid additives, the finely granulated additive does not cause a dilution effect. The breakdown of glucose (glycolysis) in venous blood samples is of great significance in pre-analytics, particularly in relation to the diagnosis of diabetes mellitus and gestational diabetes. To prevent imme-diate glycolysis in the event of delay between blood collection and measurement in the lab, test tubes should include a citrate/citric acid buffer as well as sodium fluoride (NaF).
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Bio-Rad - Preparing for a Stress-free QC Audit

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