10-minute in-clinic screening
A short workflow without a dedicated analyzer supports clinics, laboratories and field screening.
A rapid qualitative screen for antibodies to feline coronavirus-associated antigens in feline whole blood, serum or plasma. Labeled FIPV Ab, it supports assessment of FCoV exposure and antibody status; antibody positivity alone does not diagnose FIP.

Product Features
A short workflow without a dedicated analyzer supports clinics, laboratories and field screening.
The built-in control line monitors sample volume, membrane migration and reagent function.
Test device, buffer and applicable collection tools create a standardized operating set.
Lot documentation, performance evaluation, registration support and OEM/ODM customization are available.
Technical Specifications
A rapid qualitative screen for antibodies to feline coronavirus-associated antigens in feline whole blood, serum or plasma. Labeled FIPV Ab, it supports assessment of FCoV exposure and antibody status; antibody positivity alone does not diagnose FIP.
| Format | Single-use test cassette, visual readout |
|---|---|
| Target | Antibodies to feline coronavirus-associated antigens (label: FIPV Ab) |
| Intended use | Rapid qualitative screening of the target analyte in feline specimens to support veterinary assessment |
| Specimen | Feline whole blood, serum or plasma |
| Method | Colloidal gold immunochromatography (lateral flow) |
| Result type | Qualitative (positive / negative / invalid) |
| Read time | 10 minutes |
| Pack size | 10 Tests/Kit |
| Storage | 2–30°C, dry and protected from light; do not freeze |
| Kit components | Test devices, matched buffer/extraction tubes, droppers or swabs as configured, and IFU |
| Performance documentation | Product-specific analytical sensitivity, specificity, repeatability, cross-reactivity and interference data are controlled in the IFU, performance evaluation report and lot-release documentation, available to distributors, registration partners and OEM/ODM customers on request. |
| Professional-use note | For professional veterinary in-vitro diagnostic use; final procedure and claims follow the controlled IFU and local registration label. |
Testing Workflow
Bring the kit and specimen to the appropriate operating temperature; verify pouch integrity and expiry.
Feline whole blood, serum or plasma
Process the specimen with the supplied buffer and collection tool according to the controlled IFU, then load the sample well.
Start timing and read the C/T lines at 10 minutes. Do not interpret outside the IFU-defined window.
Result Interpretation
Both control line C and test line T appear. Line intensity is not a quantitative measurement.
Only control line C appears. A negative result does not exclude low analyte levels, an early window or intermittent shedding.
No control line C appears, regardless of the T line. Repeat with a new device.
FCoV antibodies can occur in healthy infected cats and cats with FIP, while confirmed FIP cases may be antibody-negative. Use as an adjunctive screen, never as a stand-alone rule-in or rule-out test for FIP.
Quality & Technical Documentation
Product-specific analytical sensitivity, specificity, repeatability, cross-reactivity and interference data are controlled in the IFU, performance evaluation report and lot-release documentation, available to distributors, registration partners and OEM/ODM customers on request.
Request IFU & Performance Data→