BD 442022 - BACTEC Plus Anaerobic/F Blood Culture Medium
The BD 442022 BACTEC Plus Anaerobic/F Medium is a specialized blood culture bottle designed for the detection of anaerobic bacteria in bloodstream infections. Manufactured by Becton, Dickinson and Company, this medium is optimized to support the growth of obligate and facultative anaerobic organisms while neutralizing commonly used antibiotics that may inhibit microbial recovery.
Developed for use with BD BACTEC automated blood culture systems, the Plus Anaerobic/F formulation plays a critical role in comprehensive sepsis diagnostics by enabling reliable detection of anaerobic pathogens that may not grow in aerobic conditions.
| Manufacturer | Application | Container Type |
| 442022 | Blood Culture Media | Container Type |
Key Benefits
This anaerobic blood culture medium enhances pathogen recovery by creating an environment favorable for anaerobic organism growth. The resin-based formulation helps absorb antibiotics present in patient blood samples, improving detection rates even in patients already receiving antimicrobial therapy.
Compatibility with automated BACTEC systems supports continuous monitoring and earlier detection of positive cultures, helping clinicians initiate targeted treatment sooner and improve patient outcomes.
Compatibility and Applications
The BD 442022 BACTEC Plus Anaerobic/F Medium is designed exclusively for use with BD BACTEC automated blood culture instruments. It integrates seamlessly into standard laboratory workflows for bloodstream infection testing.
Common applications include diagnosis of anaerobic bacteremia, sepsis evaluation, and comprehensive blood culture testing alongside aerobic bottles. It is widely used in hospital microbiology laboratories, emergency departments, and critical care settings.
Usage Guidelines
Blood should be collected using standard aseptic technique and inoculated into the bottle according to laboratory protocol, ensuring appropriate blood volume for optimal organism recovery. The bottle should then be loaded into a compatible BD BACTEC instrument for incubation and continuous monitoring.
Samples should be handled and processed in accordance with institutional microbiology guidelines to maintain accuracy and reliability of results.
Certifications, Safety Standards, and Regulatory Approvals
The BD 442022 BACTEC Plus Anaerobic/F Medium is manufactured under strict quality management systems aligned with FDA medical device regulations and internationally recognized manufacturing standards. These controls ensure consistent media performance, bottle integrity, and reliable detection sensitivity.
Regulatory compliance confirms suitability for use in regulated clinical laboratory environments across the United States.
Comparison with Competitor Products
Compared with standard anaerobic blood culture bottles, the BD BACTEC Plus Anaerobic/F Medium offers enhanced performance through its antibiotic-neutralizing resin technology and optimized anaerobic growth conditions. While some competitor bottles lack resin-based recovery support, BDs formulation improves diagnostic yield, particularly in patients receiving antibiotics.
Laboratories often select BD BACTEC anaerobic bottles for their proven reliability, system compatibility, and strong clinical validation.
Typical User Profile and Application Scenarios
Typical users include microbiologists, laboratory technologists, infectious disease specialists, and clinicians involved in sepsis diagnosis and management.
The product is especially effective in hospital laboratories, emergency departments, intensive care units, and inpatient settings where rapid, accurate detection of bloodstream infections is essential.
Best Practices for Use and Maintenance
Best practice includes collecting recommended blood volumes and pairing anaerobic bottles with appropriate aerobic counterparts for comprehensive testing. Bottles should be promptly loaded into the BACTEC system to support timely detection.
The bottle is single use and requires no maintenance. Disposal should follow biohazard waste protocols after testing is complete.
Regulatory and Safety Information
The BD 442022 BACTEC Plus Anaerobic/F Blood Culture Medium is classified as a regulated medical device and complies with applicable FDA requirements. Its design supports compliance with clinical laboratory standards and infection control policies.
Proper handling, labeling, and disposal help maintain laboratory safety and regulatory compliance.
How to Order
The BD 442022 BACTEC Plus Anaerobic/F Medium 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 product assistance, contact CIA Medical customer service at 312 275 5850 or use the contact form available on this page for prompt support.
