by Neoteryx | 1 min read
by Neoteryx | 1 min read
Mitra® microsampling devices have proven useful in a diverse array of fields – pediatrics, clinical trials, clinical and preclinical research, health and wellness, and beyond. Much of the celebration and progress of Volumetric Absorptive Microsampling (VAMS™) technology can be attributed to the creativity, ingenuity, and tenacity of our customers.
Some Mitra users have come up with more unusual uses for these versatile devices. Such creativity seems to rise during the hot, slow summer months.
Some of our favorite uses of Mitra are even more abstract, verging into the realms of pure art.
We’ve heard reports of microsamplers used to stir cocktails, rescue ants trapped in hard-to-reach places, and even build small cabins and spacecraft.
Send us photos of your most unusual and spectacular Mitra-based designs and creations, and get recognized for your ingenuity! You can email us or post on social media with the hashtags #Mitra and #Neoteryx. (We're on Twitter, Facebook, and LinkedIn.)
Need more Mitra to make your idea a reality? Get in touch.
Originally published Jul 17, 2018 9:59:19 AM, updated on November 4, 2019
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The Mitra Device is a single-use, non-sterile device used as a specimen collector and for the storage and transport of blood or other biological fluids. It is designed to be used by laboratory and healthcare professionals, or end-users as a container to collect and transport blood or other biological fluids. It is not specific to any clinical test, and is not for use in diagnostic procedures. Use of the Mitra Microsampler in Laboratory Developed Tests (LDTs) requires further processing including the establishment of performance characteristics and successful validation by the laboratory in a manner consistent with CLIA and/or other regulatory requirements.
The Mitra Microsampling Device is a FDA listed Class 1 exempt device, CE-IVD self-certified in the UK and EU, a Class I IVD in Australia, and registered with Health Canada. 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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