FAST IDENTIFICATION OF PATHOGENS

 

MariPoc system

maripoc sistema arcdia somija

What is the mariPOC® test system?

  • A new point-of-care test system for acute infections
  • First test system in the market for multianalyte POC testing
  • Automated random-access antigen detection test
  • For respiratory (swab, aspirate) and stool samples
  • IVD-CE marked

Why to choose mariPOC® for acute infection diagnostics?

  • Accuracy similar to central laboratory antigen tests
  • Easy-to-use and short hands-on-time. The first result available in 20 minutes
  • Automated results read-out
  • Replaces conventional rapid and laboratory antigen tests
  • Can be connected to laboratory information systems

What does the mariPOC® test system allow?

  • Pathogen-specific diagnosis on time
  • Accurate use of virus-specific drugs and antimicrobials
  • In-patient cohorting
  • Efficient control of patient flow
  • Improved cost-effectiveness

MariAST system

ArcDia’s mariAST® is the most promising platform to tackle antibiotic resistance.

  • Allows testing of antibiotic resistance directly from polymicrobial clinical samples
  • Is rapid and easy to use
  • Is fully automated
  • Has a high capacity: 40 -100 samples per day
  • Enables bringing AST and resistance testing in a point-of-care environment

mariAST® measures species-specific bacterial growth in real-time. mariAST® combines in-well culture and high-accuracy bacterial detection. The process yields an ID in only 20 minutes, and reports resistance results for strong positive inoculum in just 2 hours after sampling.

Pre-treatment

ArcDia’s mariAST® is based on ArcDia’s mariPOC® field-proven test system.

ArcDia’s platform:

  • Is based on the proprietary TPX detection tecnology published in Nature Biotechnology in 2000
  • Has been deployed in routine central lab and point-of-care settings since 2011
  • Has been awarded e.g. Frost & Sullivan Point-of-Care Leadership Prize in 2014
  • Whose sister technology, born and developed in ArcDia’s scientific founder’s lab in Finland, won The Nobel Prize in Chemistry in 2014

 

Cystic Fibrosis

cistiskas fibrozes noteiksana elitech group wescor

Because routinely screening newborns for cystic fibrosis leads to early diagnosis and means treatment can begin immediately.

ELITech Biomedical Systems is the acknowledged world leader for the laboratory diagnosis of cystic fibrosis with our proven Macroduct Sweat Collection System for stimulation and collection of sweat and our Sweat-Chek (total electrolyte analysis) or Chloro-Chek (Chloride titration) analyzers.

When considering a potential laboratory diagnosis of cystic fibrosis, a physician still relies heavily upon the results of the sweat test, which is capable of producing an unequivocal, quantitative result to corroborate clinical observations. The Macroduct System provides the most accurate and simple sweat test system available.

ELITech’s peerless scientific and engineering expertise has also produced Nanoduct, the completely integrated and miniaturized sweat analysis system for patients of any age.

The Nanoduct patented in-situ stimulation and analysis provide clinicians with the earliest possible laboratory diagnosis of cystic fibrosis, enabling doctors to intervene and treat this disease in the earliest days of life.

Newborn screening

newborn screening labsystems diagnostics oy

The Neonatal screening or Newborn Screening is a preventive pediatric screening service provided to all the neonates to assess the possibility of genetic disorders in the area of "Inborn Errors of Metabolism".

These errors, which are not harmful now, have all the potential to cause permanent neurological, cognitive, tactile and physical damage in the child. If such errors are detected in this newborn baby screening, they can be treated easily.

Trivitron provides a wide range Newborn Screening instruments, including Modular & Fully Automated NBS Instrumentation, manual & automated equipment and reagent kits.

Trivitron's Diagnostic division Labsystems Diagnostics OY occupies the second place in the world when it comes to New Born Screening Technology.

Our company

DIAMEDICA Latvia belongs to the DIAMEDICA OU Group, which was founded in 1991 and is owned by Baltic originated private capital. DIAMEDICA Group operates in all three Baltic countries (Estonia, Latvia and Lithuania) and has its representative offices in Tallinn, Riga and Vilnius.

DIAMEDICA Latvia actively operates since the end of 1993. DIAMEDICA operates in the field of clinical laboratory equipment, which includes distribution of analyzers, reagents and microscopes as well as hardware maintenance services. During last year’s company has expanded its operations also to hospital equipment and environmental laboratories.

ISO 9001:2015

Since 26.11.2012. Ltd. Diamedica management system is certified according to international standard ISO 9001.

ISO 9001 serifikats LVmin

 

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Augusta Deglava street 66, Riga, LV-1035

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