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our technical director is at your service

Implementing our Mitra® specimen collection, storage, and transportation devices and volumetric absorptive microsampling (VAMS®) technology is easier than you might think, but if you encounter any challenges, we are here to guide you! Our Technical Director, James Rudge, PhD, can consult with you to provide insights on set-up, processing and methodology to help support you in achieving your goals.

Schedule your consultation today

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Neoteryx, LLC

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Mitra® is an exempt medical device in the US, CE-IVD self-certified in the UK and EU, a Class 1 IVD in Australia, and registered with Health Canada. It is intended as a specimen collector and for the storage and transport of biological fluids. Use of the device with blood for diagnostic applications is limited to certain countries and, in the US, for research and non-diagnostic purposes only. Neoteryx Products are not marketed in the US for clinical diagnostic uses. In other countries, Neoteryx Products may be used in clinical diagnostic laboratory systems after the laboratory has validated their complete system in compliance with relevant rules and regulations. Neoteryx operates a Quality Management System (QMS) that is based on FDA good manufacturing practices, 21 CFR 820 regulations, and ISO-13485.

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