Three steps, one result after 10 minutes. All components are included in the kit.
Disinfect the fingertip with the alcohol swab. Prick using the single-use lancet and apply one drop of whole blood to the sample well (S).
Dispense two drops of sample diluent into the diluent well (D) using the single-use pipette. Place the cassette on a flat surface.
The control line (C) must appear. The IgM line indicates an active response. The IgG line indicates a past or convalescent exposure.
Tiered pricing applies from 50 units upward. Larger orders qualify for bonded warehousing, custom packaging, and private-label options.
| Estimated quantity (units) | Volume pricing net · USD |
|---|---|
| 1 – 2 Tests | $29.00 |
| 3 – 9 Tests | $22.79 −21 % |
| 10 – 99 Tests | $17.09 −41 % |
| 100 – 349 Tests | $13.67 −52 % |
| 350+ Tests | $11.39 −60 % |
| All prices net. Customs duties, import taxes and local VAT may apply on import and are the buyer's responsibility. | |
parahealth rapid tests are deployed at hospitals, reference laboratories, public health agencies, military medical services and humanitarian organisations.
The test supports differential diagnosis of haemorrhagic fever with renal syndrome (HFRS) and complements RT-PCR.
Sudden fever above 38.5 °C, severe back or abdominal pain, oliguria, visual disturbances or atypical pneumonia of unknown origin.
Forestry and agriculture workers, hunters, pest-control technicians, construction workers in endemic areas, and laboratory personnel with rodent contact.
After return from endemic areas or following confirmed exposure to rodent excreta, for example cellar cleanouts or camping.
HFRS against leptospirosis, sepsis, acute glomerulonephritis, and other viral haemorrhagic syndromes.
Complete technical data for the Hantavirus IgG/IgM antibody rapid test.
| Format | Cassette with combined IgG/IgM test lines and control line (lateral flow immunoassay, colloidal gold) |
| Sample types | Human serum, plasma or whole blood (capillary or venous) |
| Relative sensitivity | 98.93% (vs. reference method) |
| Relative specificity | 99.20% (vs. reference method) |
| Time to result | 10 minutes, read window 10 to 15 minutes |
| Storage | 2 to 30 °C, dark, dry, do not freeze |
| Shelf life | 24 months from manufacture, current lot Expiry 05/2028 |
| Intended user | For professional use only (in vitro diagnostic device) |
| Kit contents | 1× test cassette in foil pouch with desiccant, 1× single-use dropper, 1× sample diluent, 1× alcohol swab, 1× lancet, 1× instructions for use |
When the item is shown as in stock, orders placed on business days before 14:00 CET usually ship the same day from Berlin via DHL or DPD. Delivery within Germany usually takes 1 to 2 business days, and EU-wide delivery 3 to 5 business days. If stock is unavailable, the cart button is disabled; for larger quantities of 100 tests or more, contact info@hantatestkaufen.de to request allocation.
The assay uses recombinant nucleocapsid antigens from multiple Hantavirus species and cross-reacts with antibodies against Puumala, Dobrava-Belgrade, Hantaan, Seoul and Sin Nombre. Strain-level typing is not possible with the rapid test and should be carried out by a reference laboratory (e.g. RKI, national reference centre).
No. This IVD is approved for professional use only. Eligible buyers include medical practices, hospitals, occupational physicians, laboratories, research institutions and authorised medical professionals. If you suspect a Hantavirus infection, please contact your physician or an emergency department.
Orders ship from our EU warehouse. Place your order on a business day before 14:00 CET for same-day dispatch via DHL or DPD. Delivery within Germany takes 1 to 2 business days, EU-wide 3 to 5. Invoicing on request is available for verified medical professionals, pharmacies, clinics and public authorities, including consolidated monthly invoicing accounts.
The outbreak on the M/V Hondius involves Andes virus, a South American Hantavirus. It is the only Hantavirus type for which limited person-to-person transmission has been documented, usually after close and prolonged contact. WHO and ECDC continue to assess the risk to the general population in Europe as very low; exposed contacts are monitored through the end of the 42-day window on 21 June 2026. In Europe, Puumala and Dobrava-Belgrade remain the relevant viruses. They are transmitted through rodent excreta, not from person to person. This rapid test supports professional HFRS diagnostics when exposure and symptoms fit, but it is not a replacement for reference-laboratory screening of quarantine contacts.
We typically respond within one business day.
All rapid tests are CE certified and comply with the EU In Vitro Diagnostic Regulation.
Same-business-day dispatch via trusted carriers from our EU warehouse.
PayPal, Klarna, SEPA, credit card, and purchase on invoice for clinics and institutions.
Monday–Friday 9:00–18:00 CET. Average response time under 24 hours. Phone: +1 (786) 432-9779
