Bard Bardex Lubricath Three-Way Specialty Latex Foley Catheter With 5cc Balloon Capacity
Bard Bardex Lubricath Three-Way Specialty Latex Foley Catheter With 5cc Balloon Capacity

Bard Bardex Lubricath Three-Way Specialty Latex Foley Catheter With 5cc Balloon Capacity

Brand/Manufacturer: BARD INC
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  • FSA Approved

Bard Bardex Lubricath Three-Way Specialty Latex Foley Catheter With 5cc Balloon Capacity features a whistle tip with 2 side eyes and is commonly used after bladder surgeries such as partial cystectomy, tumor removal/fulguration, suspension, and damage associated with gynecology surgeries, or other urological procedures. The tip is medium length and is useful for removal of clots and debris. The whistle tip can be cleared easily because it is approximately the same diameter as the drainage lumen. It will not accommodate a stylet and is hydrogel coated.

Item #DescPkgPrice 
0132L24 24Fr 12/Case $580.65 $443.65

More Information

  • Cautions:
    - Do not aspirate urine through drainage funnel wall
    - Some Foley catheters may contain Natural Rubber Latex which may cause allergic reactions
    - Please check the package
    - Contains or Presence of Phthalates: Di(2-ethylhexyl)phthalate (DEHP) is a plasticizer used in some polyvinyl chloride medical devices
    - DEHP has been shown to produce a range of adverse effects in experimental animals, notably liver toxicity, and testicular atrophy
    - Although the toxic and carcinogenic effects of DEHP have been well established in experimental animals, the ability of this compound to produce adverse effects in humans is controversial
    - There is no evidence that neonates, infants, pregnant and breast feeding women exposed to DEHP experience any related adverse effects. However, a lack of evidence of causation between DEHP-PVC and any disease or adverse effect does not mean that there are no risks
    - With Temperature-Sensing Probes, in the presence of RF energy sources, local heating, temperature errors, and probe damage may occur
    - In medical use, unplug the temperature-sensing catheter at the temperature monitor before activating electrosurgical or other types of direct coupled RF energy sources.
    - Do not stretch catheter. This will cause repositioning of the probe
    - Do not use Stylet. This will cause stretching of catheter
  • Warnings:
    - On catheter, do not use ointments or lubricants having a petrolatum base. They will damage latex and may cause the balloon to burst
    - After use, this product may be a potential biohazard. Handle and dispose of in accordance with the accepted medical practice and applicable local, state and federal laws and regulations
    - Visually inspect the product for any imperfections or surface deterioration prior to use. Use Luer tip syringe to inflate with stated mL of sterile water OR for pre-filled products, remove the clip and squeeze reservoir to inflate with stated mL of sterile water
    - Store catheters at room temperature away from direct exposure to light, preferably in the original box
  • Additional Information:
    - This is a single use device. Do not resterilize any portion of this device. Reuse and/or repackaging may create a risk of patient or user infection, compromise the structural integrity and/or essential material and design characteristics of the device, which may lead to device failure, and/or lead to injury, illness or death of the patient
    - Aggressive traction, particularly in the presence of suturing is not recommended for 100% silicone catheters.
    - Should balloon rupture occur, care should be taken to assure that all balloon fragments have been removed from the patient
    - Do not exceed recommended balloon capacities
    - Sterile unless the package is opened or damaged.
    - Catheters should be replaced in accordance with the CDC guideline, "Guideline for Prevention of Catheter-Associated Urinary Tract Infection." At the onset or first signs of a urinary tract infection, catheter encrustation, or any other catheter-related adverse effect, the catheter should be replaced
  • Daily Maintenance:
    - Do not use alcohol or prepackaged bathing systems, which could lead to early lifting. If showering/bathing, cover with plastic wrap or waterproof dressing
    - Conduct skin assessment prior to application and repeat daily per facility protocol
    - Use clinical judgment on the removal of the STATLOCK® stabilization device if the patient experiences any fluid shifts that may interfere with skin integrity
    - Sterile unless the package is opened or damaged

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