10-minute in-clinic screening
A short workflow without a dedicated analyzer supports clinics, laboratories and field screening.
VETVeterinary Rapid DiagnosticsFIPV Ag
Feline Infectious Peritonitis Virus (FIPV) Antigen Rapid Test Kit
A rapid qualitative screen for feline coronavirus-associated antigen in feline feces or body-cavity effusion such as ascites, supporting initial assessment of clinically compatible cases. Labeled FIPV Ag; a single rapid result cannot independently confirm or exclude FIP.
Feline coronavirus-associated antigen (label: FIPV Ag)Feline feces or body-cavity effusion such as ascites (per controlled IFU/label)10 min10 Tests/Kit2–30°C
Product Features
Product Features
Clear C/T line interpretation
The built-in control line monitors sample volume, membrane migration and reagent function.
Matched sample preparation
Test device, buffer and applicable collection tools create a standardized operating set.
Traceable technical package
Lot documentation, performance evaluation, registration support and OEM/ODM customization are available.
Technical Specifications
Technical Specifications
A rapid qualitative screen for feline coronavirus-associated antigen in feline feces or body-cavity effusion such as ascites, supporting initial assessment of clinically compatible cases. Labeled FIPV Ag; a single rapid result cannot independently confirm or exclude FIP.
| Format | Single-use test cassette, visual readout |
|---|---|
| Target | Feline coronavirus-associated antigen (label: FIPV Ag) |
| Intended use | Rapid qualitative screening of the target analyte in feline specimens to support veterinary assessment |
| Specimen | Feline feces or body-cavity effusion such as ascites (per controlled IFU/label) |
| 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
Testing Workflow
1
Equilibrate
Bring the kit and specimen to the appropriate operating temperature; verify pouch integrity and expiry.
2
Collect specimen
Feline feces or body-cavity effusion such as ascites (per controlled IFU/label)
3
Prepare & load
Process the specimen with the supplied buffer and collection tool according to the controlled IFU, then load the sample well.
4
Timed reading
Start timing and read the C/T lines at 10 minutes. Do not interpret outside the IFU-defined window.
Result Interpretation
Result Interpretation
Positive
Both control line C and test line T appear. Line intensity is not a quantitative measurement.
Negative
Only control line C appears. A negative result does not exclude low analyte levels, an early window or intermittent shedding.
Invalid
No control line C appears, regardless of the T line. Repeat with a new device.
Clinical Interpretation
Interpret with signs, imaging, effusion cytology/biochemistry, A:G ratio and, where indicated, FCoV RNA or tissue/cellular antigen testing. A negative result does not exclude FIP.
Quality & Technical Documentation
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.
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