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BACTEC™ Standard/10 Aerobic/F Medium



Cat. # Description Qty. Unit
442260 BACTEC™ Standard/10 Aerobic/F Medium
50 SP
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Intended Use:

BACTEC™ Standard/10 Aerobic/F culture vials (enriched Soybean-Casein Digest broth with CO2) are for aerobic blood cultures. Principal use is with the BACTEC fluorescent series instruments for the qualitative culture and recovery of aerobic microorganisms (bacteria and yeast) from blood.


Catalog # Description Quantity Unit
442260 BACTEC™ Standard/10 Aerobic/F Medium
50 SP

BACTEC™ Standard/10 Aerobic/F Culture Vials
Revision: 2010/02     Revision Date: 02/01/2010    

Intended Use:

BACTEC™ Standard/10 Aerobic/F culture vials (enriched Soybean-Casein Digest broth with CO2) are for aerobic blood cultures. Principal use is with the BACTEC fluorescent series instruments for the qualitative culture and recovery of aerobic microorganisms (bacteria and yeast) from blood.



Product Summary:

The sample to be tested is inoculated into one or more vials which are inserted into the BACTEC fluorescent series instrument for incubation and periodic reading. Each vial contains a chemical sensor which can detect increases in CO2 produced by the growth of microorganisms. The sensor is monitored by the instrument every ten minutes for an increase in its fluorescence, which is proportional to the amount of CO2 present. A positive reading indicates the presumptive presence of viable microorganisms in the vial. Detection is limited to microorganisms that will grow in a particular type of medium.



User Quality Control:

Quality control requirements must be performed in accordance with applicable local, state and/or federal regulations or accreditation requirements and your laboratory's standard Quality Control procedures. It is recommended that the user refer to pertinent CLSI (formerly NCCLS) guidance and CLIA regulations for appropriate Quality Control practices.

DO NOT USE culture vials past their expiration date.

DO NOT USE culture vials that exhibit any cracks or defects; discard the vial in the appropriate manner.

Quality Control Certificates are provided with each carton of media. Quality Control Certificates list test organisms, including ATCC™ cultures specified in the CLSI Standard, Quality Control for Commercially Prepared Microbiological Culture Media.5

The range of time-to-detection in hours was ≤ 72 hours for each of the organisms listed on the Quality Control Certificate for this medium:

Streptococcus pyogenes ATCC 19615
Pseudomonas aeruginosa ATCC 27853
Alcaligenes faecalis ATCC 8750
Escherichia coli ATCC 25922
Candida albicans ATCC 18804
Haemophilus influenzae ATCC 19418
Streptococcus pneumoniae* ATCC 6305
Neisseria meningitidis ATCC 13090
Staphylococcus aureus ATCC 25923
*CLSI Strain

For information on Quality Control for the BACTEC fluorescent series instrument, refer to the appropriate BACTEC fluorescent series instrument User's Manual.



Reagents:

The BACTEC Standard/10 Aerobic/F culture vials contain the following active ingredients prior to processing:

List of Ingredients
 
  (WTR) Processed Water  40   mL
  (SCB) Soybean-Casein Digest Broth  3.0%   w/v
  (YEX) Yeast Extract  0.3%   w/v
  (ATD) Animal Tissue Digest  0.01%   w/v
  (SCR) Sucrose  0.1%   w/v
  (HEM) Hemin  0.0005%   w/v
  (MEN) Menadione  0.00005%   w/v
  (PXH) Pyridoxal HCl (Vitamin B6)  0.001%   w/v
  (SBC) Sodium Bicarbonate  0.04%   w/v
  (SPS) Sodium Polyanetholsulfonate  0.035%   w/v
 

All BACTEC media are dispensed with added CO2.



Warnings and Precautions:

For in vitro Diagnostic Use.

This Product Contains Dry Natural Rubber.

Pathogenic microorganisms, including hepatitis viruses and Human Immunodeficiency Virus, may be present in clinical specimens. "Standard Precautions"1-4 and institutional guidelines should be followed in handling all items contaminated with blood and other body fluids.

Prior to use, each vial should be examined for evidence of damage, contamination or deterioration. Vials displaying evidence of damage or contamination such as leakage, cloudiness, discoloration (darkening), bulging or depressed septum should not be used.

A contaminated vial could contain positive pressure. If a contaminated vial is used for direct draw, contaminated culture media could be refluxed into the patient's vein. Vial contamination may not be readily apparent. When using direct draw procedures, monitor the process closely to avoid refluxing materials into patient.

On rare occasions, the glass bottle neck may be cracked and the neck may break during removal of the flip-off cap or in handling. Also, on rare occasions, a vial may not be sealed sufficiently. In both cases the contents of the vial may leak or spill. If the vial has been inoculated, treat the leak or spill with caution, as pathogenic organisms/agents may be present. Before discarding, sterilize all inoculated vials by autoclaving.

Positive culture vials for subculturing or staining, etc.: Before sampling it is necessary to release gas which often builds up due to microbial metabolism. Sampling should be performed in a biological safety cabinet if possible, and appropriate protective clothing, including gloves and masks, should be worn. See Procedure section for more information on subculturing.

To minimize the potential of leakage during inoculation of specimen into culture vials, use syringes with permanently attached needles or Luer-Lok™ brand tips.



Information shown on this page is a short summary extracted from the Package Insert, available as a PDF under the Related Documents section of this page.