the microsampling blog In some territories, which are listed in our website footer, our microsampling devices are supplied for therapeutic or IVD use as referenced in some of our content. Outside of those territories our devices are supplied for research use only (RUO).
Christa Nuber

Christa Nuber

Recent Posts by Christa Nuber:

COVID-19 & workplace safety: vaccines & antibodies

by Christa Nuber | 6 min read

COVID-19 & workplace safety: vaccines & antibodies

In early May 2021, the Centers for Disease Control and Protection (CDC), relaxed their face masking and social distancing restrictions for people who were fully vaccinated against SARS-CoV-2, the virus …

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what is the shelf life of blood and journey of a blood sample?

by Christa Nuber | 5 min read

what is the shelf life of blood and journey of a blood sample?

Once a blood sample has been collected and labeled, it must be delivered, shipped or otherwise transported to a lab for testing. What is the shelf life of blood samples? …

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why are antibodies critical in our battle against COVID-19?

by Christa Nuber | 7 min read

why are antibodies critical in our battle against COVID-19?

Production of antibodies are part of the body's defense mechanism. They help our immune systems fight off contagious disease and reinfection. This is the concept behind vaccinations. A vaccination, such …

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Mitra® devices are intended as a specimen collector and for the storage and transport of blood. They are CE-IVD in the UK and EU, a Class 1 IVD in Australia, Brazil & China, Class B in South Africa, and registered with health agencies in Canada and Ukraine. 

In the USA, Mitra devices are supplied as a Research-Use Only (RUO) product, to assist in method development, other research-related and non-diagnostic activities. Mitra has not been validated for use with any diagnostic testing. The suitability of Mitra for any analytical application must be evaluated and validated by the laboratory or research institute in a manner consistent with local regulatory requirements. 

hemaPEN® is supplied for therapeutic or IVD use in Australia, New Zealand, UK, EU and USA only: ARTG number: 280007; CE mark, general IVD; US FDA number: D410490. Outside of the territories listed above, the hemaPEN is supplied for research use only (RUO) and not for therapeutic or diagnostic use. 

Mitra®, VAMS® & hemaPEN® are registered trademarks owned by entities in the Trajan Group. 

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