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Sabervet Avian Influenza Virus H7 Antigen Rapid Test
GMP Certified
A Specialized Brand by ITGen

Sabervet Avian Influenza Virus H7 Antigen Rapid Test

As a vital part of avian biosecurity, the SaberVet AIV H7 Ag Rapid Test offers a fast and accurate solution for detecting H7 subtype specific antigens in laryngeal or cloacal specimens. This user-friendly kit provides visual, easy-to-interpret results within a 5-10 minute window, allowing for immediate quarantine and response. Performance characteristics highlight its accuracy, with a diagnostic sensitivity of 96.67% (145/150) and a specificity of 97.65% (166/170). SaberVet combines advanced antibody technology with practical field utility, making it a reliable choice for monitoring high-consequence avian influenza strains in diverse poultry environments.

Sensitivity
96.67%
Specificity
97.65%
Reaction Time
5-10 mins
Shelf Life
36 months (when stored unopened at 2–30°C) / Final expiration date is indicated on the package.
Technical Data

Product Parameters

Engineered for precision, built for reliability

Specimen Type
Secretions/Cloaca
Detection Method
Colloidal Gold Immunoassay
Format
Cassette
Result Time
10 minutes
Sensitivity
96.67%
Specificity
97.65%
Storage Conditions
2-30°C / 35.6-86°F
Shelf Life
36 months (when stored unopened at 2–30°C) / Final expiration date is indicated on the package.
Packaging
20 Tests/Box
Certifications
CE, ISO 13485 & GMP certified
OEM/ODM Service
Available

Clear Results, Confident Diagnosis

Eliminate diagnostic uncertainty with our advanced colloidal gold technology that delivers crystal-clear test lines and reliable results every time.

SaberVet Advantage

Clear SaberVet test results
  • Deep red, crystal-clear T-lines
  • Clean, interference-free background
  • GMP-controlled batch consistency
  • Confident, reliable diagnosis

Simple 4-Step Protocol

Streamlined workflow for accurate results in minutes

1

Sampling

Collect fecal sample using provided swab

2

Dilution

Mix sample thoroughly in assay buffer tube

3

Loading

Add 3 drops to sample well (S) on test device

4

Interpret

Read results after 5-10 minutes

Scientific Validation

Rigorous testing ensures diagnostic confidence

Clinical Performance vs PCR Gold Standard

Clinical Sensitivity 97.6%
Clinical Specificity 98%
Overall Accuracy 98.8%

Study Details: Comparative analysis conducted on 500 clinical samples across 3 different production lots, ensuring batch-to-batch consistency and reliability.

Complete Kit Components

Everything you need for accurate testing

Test Device

Individual foil pouch with desiccant

Assay Buffer

Pre-measured extraction tube

Disposable Swab

Sterile sampling swab

Instructions

Detailed IFU manual

Work Station

Organized Diagnostic Card Station

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