Rapid canine distemper test SaberVet CDV/CPV Ab

veterinaryfor caninesfor dogs

Product overview
SaberVet Canine Distemper Virus/Parvo Virus Antibody Combo Rapid Test is a lateral flow immunoassay for the simultaneous qualitative detection of antibodies to canine distemper virus (CDV) and canine parvovirus (CPV) in canine whole blood, serum and plasma at point-of-care or field settings.

Key benefits

• Simultaneous CDV and CPV antibody detection to assess combined immunization status.
• Provides rapid, on-site results to inform vaccination and booster decisions.
• Helps identify inadequate immunity to reduce disease incidence and associated costs.
• Supports veterinarians in clinical decision-making and herd/patient health management.

Disease prevention and control measures

• Maintain recommended vaccination schedules and administer boosters as indicated by serological status.
• Implement hygiene and disinfection protocols in kennels and clinical environments to limit pathogen spread.
• Quarantine and screen new or symptomatic animals prior to group introduction.
• Avoid high-risk environments during outbreaks to reduce exposure.
• Ensure regular health checks and appropriate nutrition to support immune competence.

Product description (technical summary)
The kit consists of lateral flow test cards designed for rapid, qualitative point-of-care assessment of vaccine-induced or natural antibodies to CDV and CPV. Manufactured in China under CE, ISO 13485, ISO 9001 and GMP systems with documented batch consistency, QC and traceability.

Technical specifications

• Brand: SaberVet
• Manufacturer: ITGen / Antigenne
• Intended use: Lateral flow immunoassay for simultaneous qualitative detection of antibodies to Canine Distemper Virus (CDV) and Canine Parvo Virus (CPV)
• Test format: Rapid test card (lateral flow)
• Analytes detected: Anti-CDV and anti-CPV antibodies
• Sample types: Canine whole blood, serum, plasma
• Result type: Qualitative (simultaneous detection for CDV and CPV)
• Clinical sensitivity: 99% (reported in clinical trials)
• Clinical specificity: 98.8% (reported in clinical trials)
• Shelf life: 24 months
• Storage conditions: 2–30°C (suitable for room-temperature field use)
• Certifications: CE, ISO 13485, ISO 9001, GMP
• Quality assurance: Batch consistency testing, in-process QC and full batch traceability
• Origin: Produced in China
• Commercial options: OEM/ODM, bulk and small-order options; packaging and customization available (MOQ and terms vary)