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    parahealth diagnostics · Hantavirus antibody test
    parahealth diagnostics logo · rapid tests and home diagnosticsRG-RNPT96027-01

    Hantavirus IgG/IgM rapid test for professional diagnostics

    A CE-IVD lateral-flow rapid test for the qualitative detection of Hantavirus IgG and IgM antibodies in serum, plasma or whole blood. Built for fast serological orientation in clinical suspicion, occupational screening, and outbreak settings.

    International orders fulfilled by buyhantatest.com

    10 min
    Time to result
    3
    Serum, plasma, whole blood
    CE-IVD
    for professional use
    05/2028
    current batch good through
    Product data
    IgG / IgM
    IgM
    Marker
    IgG
    Marker
    SKU
    RG-RNPT96027-01
    Test method
    Lateral-flow rapid test
    Marker
    IgG and IgM antibodies
    Sample type
    Serum, plasma or whole blood
    Status
    Professional IVD test
    Trusted worldwide

    Used in hospitals, public health, and humanitarian programs.

    350k+
    Customers worldwide
    30+
    Countries served
    30k+
    Business accounts
    University Hospital · EU
    Occupational Health Clinic · DACH
    Public Health Authority
    Military Medical Service
    Reference Laboratory
    Humanitarian Reserve
    Use cases

    Fast serological orientation when time and context matter.

    Clinical suspicion

    Supports serological assessment of suspected Hantavirus infection presenting with renal or pulmonary symptoms.

    Occupational health

    Relevant for occupations exposed to rodent excreta: forestry, agriculture, warehousing, lab work, and pest control.

    Outbreak & screening

    Helps with decentralized triage and contact assessment when central lab turnaround is too slow or operationally complex.

    Test procedure

    A clear workflow for point-of-care teams.

    01 · Sample

    Apply the sample

    Serum, plasma or whole blood is dispensed into the test cassette.

    02 · Buffer

    Add diluent

    The sample buffer drives the chromatographic flow across the test lines.

    03 · Read

    Interpret the result

    IgM, IgG and the control line are read visually after approximately 10 minutes.

    Specifications

    The key data at a glance.

    Format
    Test cassette with separate IgG/IgM test lines
    Storage
    2-30 °C
    Manufacturer reference
    RNPT96027-01
    Kit contents
    Cassette, dropper, sample buffer, alcohol wipe, lancet, instructions for use
    Regulatory context

    Positioned for professional in-vitro diagnostics.

    The Hantavirus IgG/IgM rapid test is part of the parahealth diagnostics portfolio and intended for professional users. Bormann Bioscience links the product portfolio, distribution, and international purchase flow through the dedicated storefront.

    CE-IVD marked
    ISO 13485 manufacturing environment
    For Professional Use Only
    International purchase flow via buyhantatest.com
    FAQ

    Frequently asked questions.

    How accurate is the Hantavirus rapid test?

    IgM and IgG performance results are provided separately in the manufacturer's instructions for use, Rev. A1 (14 May 2026), relative to a comparative reagent. Consult the current instructions for the full tables and confidence intervals.

    Which Hantavirus strains does it detect?

    The test detects antibodies against Puumala, Dobrava, Hantaan and Seoul virus. Strain-level differentiation is not possible with serology and requires PCR or sequencing.

    Is this test intended for home use?

    No. It is an in-vitro diagnostic intended for professional users (clinic, hospital, lab, pharmacy). If you suspect a Hantavirus infection, seek medical advice immediately.

    How fast is shipping and is invoicing available?

    Shipping leaves the EU warehouse within 1–2 business days. Invoice payment is available for clinics, practices and institutional customers. Volume orders are quoted individually.

    What does the current Andes Hantavirus outbreak mean for me?

    Andes-specific tests are in development. This kit covers the classic European and Asian Hantavirus strains and is suited for outbreak settings outside South America.

    What is the regulatory status of the test?

    CE-IVD marked under IVDR. Manufactured in an ISO 13485-certified environment. For professional use as labeled.

    Order or request a B2B quote

    Hantavirus rapid test for practices, hospitals, pharmacies and institutions.

    Individual orders go through buyhantatest.com. For volume, resale or institutional procurement, we consult directly.