BD 442023 - BACTEC Plus Aerobic/F Culture Media Bottle for Blood Culture Detection, 50/PK

BD 442023 - BACTEC Plus Aerobic/F Culture Media Bottle for Blood Culture Detection, 50/PK

The BD 442023 BACTEC Plus Aerobic/F Media is a specialized blood culture medium designed for the rapid detection of aerobic and facultative anaerobic microorganisms from blood specimens. Developed for use with BD BACTEC automated blood culture systems, this media supports early and reliable detection of bloodstream infections, which is critical for timely clinical intervention.

The formulation includes resin technology that helps neutralize antibiotics commonly present in patient blood samples, improving microorganism recovery rates. This makes the BACTEC Plus Aerobic/F Media particularly valuable in patients who have already received antimicrobial therapy.

Key Benefits

This media enhances diagnostic accuracy by supporting robust growth of aerobic and facultative organisms, even in the presence of antimicrobial agents. The antibiotic-neutralizing resin helps reduce false-negative results and improves detection sensitivity.

Its compatibility with automated blood culture systems streamlines laboratory workflows, reduces manual handling, and supports faster time to detection. Consistent media quality contributes to dependable, reproducible results that clinicians can trust when making treatment decisions.

Compatibility and Applications

BD 442023 BACTEC Plus Aerobic/F Media is designed specifically for use with BD BACTEC blood culture instruments and associated laboratory workflows.

It is widely used in hospital microbiology laboratories, emergency departments, intensive care units, and reference laboratories. Typical applications include the detection of bacteremia, septicemia, and other bloodstream infections in adult and pediatric patient populations, depending on institutional protocols.

Usage Guidelines

Blood specimens should be collected using aseptic technique and inoculated directly into the culture bottle according to facility guidelines. The bottle is then loaded into the compatible BD BACTEC system for continuous monitoring and detection.

Handling, incubation, and disposal should follow laboratory standard operating procedures and manufacturer recommendations to ensure optimal performance and biosafety.

Certifications, Safety Standards, and Regulatory Approvals

BD BACTEC Plus Aerobic/F Media is manufactured under stringent quality control systems to ensure consistency, sterility, and performance reliability.

The product complies with FDA requirements for in vitro diagnostic use and aligns with recognized clinical microbiology standards, reinforcing its suitability for regulated diagnostic environments.

Comparison with Competitor Products

Compared with conventional aerobic blood culture media, the BD BACTEC Plus Aerobic/F Media offers enhanced microorganism recovery due to its antibiotic-neutralizing resin technology. While some competing media may support aerobic growth, they may be less effective in samples from patients receiving antimicrobial therapy.

Laboratories often choose BD BACTEC media for its proven integration with automated systems, dependable detection performance, and long-standing clinical acceptance.

Typical User Profile and Application Scenarios

This product is primarily used by clinical microbiologists, laboratory technologists, and pathology staff responsible for blood culture processing and infection diagnostics.

It is especially effective in acute care hospitals, critical care settings, and emergency departments where rapid detection of bloodstream infections is essential for patient outcomes.

Best Practices for Use and Maintenance

Proper blood volume collection according to institutional guidelines helps optimize detection sensitivity. Bottles should be stored and handled as recommended to maintain media integrity.

Strict adherence to aseptic collection techniques and timely loading into the automated system help ensure accurate and reliable results while minimizing contamination risk.

Regulatory and Safety Information

Use of BD 442023 BACTEC Plus Aerobic/F Media supports compliance with FDA in vitro diagnostic regulations and laboratory biosafety standards. All specimens and used culture bottles should be handled and disposed of in accordance with local, state, and federal biohazard regulations.

How to Order

To order BD 442023 BACTEC Plus Aerobic/F Media, add the product to your cart and complete the checkout process on the CIA Medical website.

For bulk purchasing, laboratory supply programs, or technical support, contact CIA Medical customer service at (312) 275-5850 or use the contact form on this page.