BD 220220 - Universal Viral Transport Vial 3 mL, 50/Pk

BD 220220 - Universal Viral Transport Vial 3 mL, 50/Pk

The BD 220220 Universal Viral Transport Vial 3 mL is a sterile specimen transport solution designed to preserve viral samples during collection, storage, and transport to the laboratory. Manufactured by Becton, Dickinson and Company, this vial contains a balanced transport medium formulated to maintain viral viability and nucleic acid integrity, supporting accurate downstream diagnostic testing.

The 3 mL fill volume provides sufficient medium to stabilize specimens collected via swabs or other approved collection devices. Its universal formulation supports a broad range of viral pathogens, making it suitable for routine and outbreak-related diagnostic workflows.

Key Benefits

This viral transport vial helps maintain specimen integrity from the point of collection through laboratory processing, reducing degradation that could compromise test accuracy. The prefilled, ready-to-use format improves workflow efficiency and minimizes preparation steps in clinical settings.

Sterile, single-use construction supports infection control and reduces contamination risk. The standardized 3 mL volume supports consistent specimen-to-medium ratios, improving reproducibility across testing platforms.

Compatibility and Applications

The BD 220220 vial is compatible with commonly used viral specimen collection swabs and integrates seamlessly into standard virology and molecular diagnostic workflows. It supports use with a wide range of laboratory testing methods, including viral culture where applicable and molecular assays such as PCR.

Typical applications include collection and transport of respiratory, nasopharyngeal, oropharyngeal, and other viral specimens in hospitals, outpatient clinics, urgent care centers, public health laboratories, and diagnostic reference labs.

Usage Guidelines

Specimens should be collected using approved swabs and immediately placed into the viral transport vial using aseptic technique. The vial should be securely capped and labeled according to institutional protocol.

Samples should be transported to the laboratory following recommended temperature and time guidelines to preserve specimen quality and testing accuracy.

Certifications, Safety Standards, and Regulatory Approvals

The BD 220220 Universal Viral Transport Vial is manufactured under quality management systems aligned with FDA medical device regulations and internationally recognized manufacturing standards. These controls help ensure sterility, formulation consistency, and container integrity.

Regulatory compliance supports its use in regulated clinical and laboratory environments across the United States.

Comparison with Competitor Products

Compared with non-universal or limited-scope transport media, the BD Universal Viral Transport formulation supports a broader range of viral pathogens and testing workflows. While some competitor products are optimized for specific assays only, BDs universal design provides flexibility for laboratories managing diverse diagnostic needs.

Healthcare facilities often prefer BD viral transport products for their consistent quality, reliable performance, and compatibility with established laboratory protocols.

Typical User Profile and Application Scenarios

Typical users include nurses, physicians, medical assistants, laboratory technicians, and public health professionals responsible for specimen collection and handling.

The vial is especially effective in hospitals, outpatient clinics, urgent care centers, emergency departments, and public health screening programs where timely and accurate viral diagnostics are critical.

Best Practices for Use and Maintenance

Best practice includes verifying specimen type compatibility and following proper collection and labeling procedures. The vial should remain sealed until use and handled only by trained personnel.

As a single-use diagnostic device, no maintenance is required. Used vials should be disposed of according to biohazard waste protocols after laboratory processing.

Regulatory and Safety Information

The BD 220220 Universal Viral Transport Vial 3 mL is classified as a regulated medical device and complies with applicable FDA requirements. Its design supports adherence to clinical laboratory standards, infection control policies, and specimen transport regulations.

Proper handling, storage, and disposal help ensure safe, compliant use and reliable diagnostic outcomes.

How to Order

The BD 220220 Universal Viral Transport Vial 3 mL is available for purchase through the CIA Medical website. Add the product to your cart and proceed through the secure checkout process.

For bulk purchasing, laboratory contracts, or additional assistance, contact CIA Medical customer service at 312 275 5850 or use the contact form available on this page for prompt support.