
Risultati per CE marked molecular analysis test kit
Di seguito l'elenco dei risultati di ricerca trovati rilevanti per la keyword 'CE marked molecular analysis test kit':
Risultati maggiormente rilevanti:
novacyt launches two new ce-ivd marked molecular diagnostic kits - novacyt
The new molecular kits have been developed to provide quantitative detection of viral DNA extracted from blood plasma and urine (BKV kit), or blood plasma and whole blood (EBV kit) from immunocompromised patients. The kits have been designed to run using the Roche LightCycler 480 PCR instrument.
products - best-in-class assays & reagents - invivoscribe
EXPLORE PRODUCTS Best-in-class assays & reagents Invivoscribe provides a full range of standardized CE-marked in vitro diagnostic cGMP products for hematology-oncology, as well as RUO assays, analyte specific reagents (ASRs), and DNA & RNA controls. Next-Generation Sequencing
covid-19 in vitro diagnostic devices and test methods database
The objective of the JRC COVID-19 In Vitro Diagnostic Devices and Test Methods Database is to collect in a single place all publicly available information on performance of CE-marked in vitro diagnostic medical devices (IVDs) as well as laboratory-developed devices and related test methods for COVID-19.
Altri risultati:
oncomate™ msi dx analysis system | ce-marked ivd | msi diagnostic test ...
The OncoMate™ MSI Dx Analysis System is a CE-Marked IVD Medical Device, leveraging the same informative MSI loci relied on by global clinical researchers for almost two decades. The improved system is designed for use as a diagnostic with cancer patients to better inform testing and treatment options.
oncomate™ msi dx analysis system | ce-marked ivd | msi diagnostic test ...
CE-Marked IVD Medical Device for MSI testing of solid tumors. PCR-based fragment-sizing test used to determine microsatellite instability (MSI ... The OncoMate™ MSI Dx Analysis System is designed to provide physicians with a functional, molecular measurement of the level of DNA mismatch repair deficiency demonstrated within their patient ...
rapid assessment of selected commercial molecular diagnostic tests for ...
months, or until a suitable device is CE marked or there is a sufficient capacity of a CE-marked equivalent product available in the UK. In parallel with the application for derogation from CE marking, PHE proactively commenced a programme of commercial kit assessments on the 3. rd. February 2020 to
qiagen launches artus prep& as ce-marked sars-cov-2 test offering up ...
QIAGEN’s innovative Prep&Amp technology integrates sample preparation and detection in a single kit, enabling throughput of more than 670 tests per PCR cycler in an eight-hour shift CE-IVD marking for Europe and other countries worldwide, EUA (Emergency Use Application) submission made in the U.S.
Last Search Plugin 2.03