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VIA Featured Innovations

  • MiraCradle™ – Neonate Cooler

    Regulatory Approvals:CE, ISO 13845

    MiraCradle™ – Neonate Cooler is an affordable passive cooling device which uses the advanced savE® Phase Change Material (PCM) technology to induce therapeutic hypothermia among newborns suffering from birth asphyxia.  It is easy to use, safe, light weight, portable and gives the precise temperature control of 33-34°C for a period of 72 hours with minimal manual supervision and no requirement of constant electricity supply.

  • MTTS Firefly Phototherapy

    The MTTS Firefly is a state-of- the-art phototherapy device designed for effective treatment of neonatal jaundice. The machine features intuitive design, double-sided lighting, compact size, user-friendly control panel, and removable single-infant bassinet. Firefly is designed to treat newborn jaundice in the mother’s room – the best way to support mother-child bonding and breastfeeding.

    Regulatory Approvals: CE Mark

  • Bempu Hypothermia Device

    Bempu is a simple, innovative bracelet which detects and alerts in the event of hypothermia, facilitating improved thermal care of newborns.

  • Arbutus Drill Cover

    The Arbutus Drill Cover is a sterilizable, reusable, fully-sealed water-proof barrier and interface that allows surgeons to safely use a low-cost hardware drill within a sterile surgical environment, and has treated over 4,000 patients to date across a number of emerging markets and emergency relief situations.

Popular Product Categories

Latest Cardiology Products

  • AED 7000 Automatic External Defibrillator

    Automatic External Defibrillator AED 7000, which is a defibrillation device safe, portable and easy to use, can be applied in family and public place to give first aid for the sudden death symptom.

  • ZOLL AED Plus Defibrillator

    The AED Plus (Semi or fully automatic) Defibrillator is an advanced clinical technology which is the only AED that can actually see when you are doing CPR and help you do it well. The AED Plus features Real CPR Help®, a unique CPR feedback tool that is able to monitor CPR quality and provide real-time feedback of chest compressions.

    Regulatory Approvals: FDA, CE

  • ZOLL R-Series BLS Defibrillator

    The R-Series BLS Defibrillator is a simple, smart, and ready technology provided to hospitals with care to detail.It is flexible solution to multiply needs with its Basic, OneStep pacing or OneStep pacing & pulse ox versions.

    Regulatory Approvals: FDA, CE

  • Zoll R-Series ALS Defibrillator

    The R-Series ALS Defibrillator is a simple, smart, and ready technology provided to hospitals with extensive care to detail. It is flexible solution to multiply needs with its advanced variations: only OneStep Pacing; OneStep Pacing & SpO2; OneStep Pacing &SpO2 & EtCO2 or with OneStep Pacing & SpO2, NIBP, & EtCO2.

    Regulatory Approvals: FDA, CE

  • DR181 series Digital Holter Recorder, 12-lead

    The DR181 has a 12-lead configuration in addition to its 3- and 5-lead versions. It is a high-quality research and clinical evaluation tool which records 12-lead / 9 channels of data without any use of arithmetically derived or reconstructed data from non-standard Holter lead hook-ups.

    Regulatory Approvals: ISO, CE, FDA

  • DR181 series Digital Holter Recorder, 3CH

    The DR181 3CH (3 channel) comes in 5- or 7-lead configuration. It is designed following three vital goals: ease-of-use for the patient and clinician, accuracy of the data and durability of the unit.

    Regulatory Approvals: ISO, CE, FDA

  • Holter LX Event Software

    The LX® Event Software is a valuable piece of the Holter system which significantly raises the standards of convenience and flexibility for handling ECG data especially when used with NorthEast's DR200/HE Combination Holter + Event recorder or DR200/E “Tel-a-heart” event recorder and the LX Remote software. LX Event is also compatible with event recorders from other manufacturers.

    Regulatory Approvals: ISO, CE, FDA

  • Holter LX Analysis Software Kit

    The Holter LX® software latest version comes in five levels of functionality: Basic, Enhanced, Enhanced Plus, Pro and Edit. Each level is tailored to address the up-to-date necessities of contemporary medicine.

    Regulatory Approvals: ISO, CE, FDA

  • DR200/HE “Tel-a-heart” Holter and Event Recorder

    The DR200/HE is a unique comfortable single unit Holter plus Event recorder. Its compact design allows for deployment with the patients but not at the expense of any of the features of the DR200/H Holter monitor and the DR200/E “Tel-a-heart™” Event recorder in one unit. This product is the optimal choice for maintaining compact inventory combining the best of two different products.

    Regulatory Approvals: ISO, CE, FDA

  • DR200/E “Tel-a-heart” Event Recorder

    The DR200/E “Tel-a-heart™” is the first of the DR200 series of Event Recorders. It comes with several versions to match the entire range of requirements for ambulatory event recorders.

    Regulatory Approvals: ISO, CE, FDA


Latest Audiology Products

  • TYM Otoscope

    Turn your smartphone into a high quality otoscope.

  • Emoyo KUDUwave

    Regulatory Approvals: IEC, FDA

    The KUDUwave™ was designed with one aim in mind – to make hearing testing and diagnosis accessible, accurate and dependable and most importantly, mobile.

Life Assay Test-it Kits Now Available

  • Test-It Syphilis Whole Blood Test

    The assay is used as a screening or confirmatory test for T. pallidum infection (also known as Syphilis).

    Regulatory Approvals: ISO 9001, ISO 13485

  • Test-It HIV Nano & Nano24 Test Kit

    Test‐it™ HIV nano range of HIV tests are ultra-modern 3rd and 4th generation qualitative immunoassays utilising the latest cutting edge technology to detect Human Immunodeficiency Virus types 1 and 2 (HIV‐1 and HIV‐2).

    Regulatory Approvals: ISO 9001, ISO 13485

  • Test-It Glutaraldehyde Test Strips

    Test-it™ Glutaraldehyde Test Strips can be used for validating that glutaraldehyde has been completely removed from disinfected surfaces.

    Regulatory Approvals: ISO 9001, ISO 13485

  • Test-It Pregnancy Test

    Immunoassay for Human Chorionic Gonadotropin (HCG) in Human Urine

    Regulatory Approvals: ISO 9001, ISO 13485

  • Test-It Brucella Lateral Flow Assay

    Life Assay manufactures the Test‐itTM range of Brucella IgM and IgG lateral flow assays for serodiagnosis of brucellosis in humans.

    Regulatory Approvals: ISO 9001, ISO 13485

  • Test-It Urinalysis Kit

    Urine Reagent Strips (URS) are used for quick and simultaneous semi- quantitative and qualitative screening of multiple urine parameters in one easy testing format.

    Regulatory Approvals: ISO 9001, ISO 13485

  • Test-It Leptospira Test Kit

    Life Assay manufactures the Test-it™ Leptospira IgM lateral flow assay for the rapid serodiagnosis of leptospirosis.

    Regulatory Approvals: ISO 9001, ISO 13485

  • Test-It Typhoid Test Kit

    Typhoid IgM lateral flow assay for serodiagnosis of typhoid fever in humans.

    Regulatory Approvals: ISO 9001, ISO 13485


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