Bard Bardex Lubricath Two-Way Specialty Latex Foley Catheter With 30cc Balloon Capacity

Bard Bardex Lubricath Two-Way Specialty Latex Foley Catheter With 30cc Balloon Capacity

Brand/Manufacturer: BARD INC
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  • Prescription required
  • FSA Approved

Bard Bardex Lubricath Two-Way Specialty Latex Foley Catheter With 30cc Balloon Capacity provides smoother insertion and enhanced patient comfort through the hydrogel coatings unique ability to absorb fluid, thus creating a hydrophilic cushion between the catheter surface and the urethra. Hydrogel coating maintains its integrity throughout the course of use, resulting in less trauma upon removal.

Lubricath Two-Way Specialty Latex Foley Catheter Features:

  • Short Round tip
  • Two opposing drainage eyes
  • Allows atraumatic insertion for enhanced patient comfort

Item # Desc Pkg Price
0118L16 16 Fr Each
0118L16 18 Fr Each
0118L16 16 Fr 6/Pack
0118L16 16 Fr 12/Pack

More On Lubricath 2-Way Specialty Foley Catheter


  • Do not aspirate urine through drainage funnel wall
  • Some Foley catheters may contain Natural Rubber Latex which may cause allergic reactions
  • Please check 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 the catheter


  • 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


Particulars Specifications
Catheter Tip Short Round Tip
Catheter Material Latex
Gender Unisex
Catheter Coating Hydrogel Coated
Catheter Style Coated Catheters
Catheter French Size 16FR
Ballon Size (CC) 30cc
Drainage Eyes Two Opposing Eyes

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