remote-dried-blood-capilllary-sampling

our venipuncture alternative gives gold-standard results without traditional blood tubes

 

Better Blood Collection for Vulnerable Patients
venipuncture-alternative-capillary-blood-sampling

To better serve pediatric patients, the elderly, and other vulnerable populations, leaders in healthcare are looking for an alternative to venipuncture. They're discovering the revolutionary capabilities of breakthrough Volumetric Absorptive Microsampling (VAMS®) technology - a smarter blood collection system using Mitra® devices to streamline clinical processes, improve the patient experience, and generate gold-standard data.

case-studies-covers
Now it's your turn! Download these case studies to see how large and small organizations use microsampling technology as a more convenient and comfortable next-generation dried blood spot.

  • Produce bioanalytical results from Mitra® samples that bridge to plasma references
  • Store Mitra® blood specimens at room temperature with excellent stability
  • Enable simple, cost-effective remote sampling for patient monitoring 
  • Collect accurate, precise blood samples without trained clinical staff 

Drop us a line

Neoteryx, LLC

421 Amapola Ave
Torrance, CA 90501
Call us: 1 (310) 787-8747
info@neoteryx.com

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.

Copyright © 2019 Neoteryx, LLC. All rights reserved.