VETVeterinary Rapid DiagnosticsFIPV Ab

Feline Infectious Peritonitis Virus (FIPV) Antibody Rapid Test Kit

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.

Antibodies to feline coronavirus-associated antigens (label: FIPV Ab)Feline whole blood, serum or plasma10 min10 Tests/Kit2–30°C
Feline Infectious Peritonitis Virus (FIPV) Antibody Rapid Test Kit
Safheal FIPV Ab · 10 Tests/Kit

Product Features

Product Features

10-minute in-clinic screening

A short workflow without a dedicated analyzer supports clinics, laboratories and field screening.

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 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.

FormatSingle-use test cassette, visual readout
TargetAntibodies to feline coronavirus-associated antigens (label: FIPV Ab)
Intended useRapid qualitative screening of the target analyte in feline specimens to support veterinary assessment
SpecimenFeline whole blood, serum or plasma
MethodColloidal gold immunochromatography (lateral flow)
Result typeQualitative (positive / negative / invalid)
Read time10 minutes
Pack size10 Tests/Kit
Storage2–30°C, dry and protected from light; do not freeze
Kit componentsTest devices, matched buffer/extraction tubes, droppers or swabs as configured, and IFU
Performance documentationProduct-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 noteFor 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 whole blood, serum or plasma

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

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

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