Diagnostic rapid test SaberVet

veterinaryfor caninesfor antibodies

Product Overview
SaberVet Canine Parvovirus Antibody Rapid Test is a lateral flow immunoassay for qualitative detection of antibodies to Canine Parvovirus (CPV) in whole blood, serum or plasma. The test provides a rapid presence/absence assessment and is intended to support evaluation of post-vaccination antibody response in veterinary practice and field settings.

Key features

• Lateral flow immunoassay for rapid, on-site testing
• Sample types: whole blood / serum / plasma
• Rapid results: 5–10 minutes
• High reported clinical sensitivity and specificity
• Simple operation suitable for clinic and field use
• Manufactured in China in a CE, ISO 13485 & GMP certified facility
• Sold by Hangzhou Antigenne Technology Co., Ltd

Intended use and clinical context
This rapid antibody test is intended for veterinary professionals to detect CPV antibody presence after vaccination, enabling confirmation of immunization success, identification of non-responders, guidance on booster vaccination needs, monitoring of immunity durability and supporting individualized vaccination planning.

Performance and reliability

• Reported clinical sensitivity: 99%
• Reported clinical specificity: 98.8%
• Batch-level quality control and consistency testing performed for each production lot

Additional product information
The test is designed for use by veterinary clinics and field teams, with room-temperature storage convenience (2–30 °C) and compatibility with standard serological sample types. Manufacturer services include OEM/ODM, private labelling and custom packaging. Global logistics options, including express and cold-chain support when required, are available from the seller.

Characteristics / technical specifications

• Product name: SaberVet Canine Parvovirus Antibody Rapid Test
• Format: Lateral flow immunoassay (rapid test cassette)
• Target: Canine Parvovirus antibody (qualitative detection)
• Sample type: Whole blood / Serum / Plasma
• Result time: 5–10 minutes
• Intended use: Qualitative detection of CPV antibodies; evaluation of vaccination effect or presence/absence of antibodies
• Sensitivity: 99% (reported from clinical trials)
• Specificity: 98.8% (reported from clinical trials)
• Shelf life: 24 months
• Storage conditions: 2–30 °C (room temperature storage)
• Manufacturing / Certifications: CE, ISO 13485, ISO 9001, GMP
• Quality assurances: Batch consistency testing, rigorous QC at every production stage, complete batch traceability and documentation
• Manufacturer / Seller: Hangzhou Antigenne Technology Co., Ltd (production in China)
• Available services: OEM/ODM, private label, custom packaging, global logistics with express and cold-chain options