Bard Interglide Pediatric And Female Vinyl PVC Intermittent Catheter
Bard Interglide Pediatric And Female Vinyl PVC Intermittent Catheter

Bard Interglide Pediatric And Female Vinyl PVC Intermittent Catheter

Brand/Manufacturer: BARD INC
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Bard Interglide Pediatric And Female Vinyl PVC Intermittent Catheter features hydroglide coating and non-slip finger grip for enhanced control. This single-use catheter is latex-free and sterile.

Item #DescPkgRewardPrice 
430614 14FR, 6" Long Each $0.06
$6.88
$2.99
430614 14FR, 6" Long 25/Case $1.24
$129.99
$61.99
431010 10FR, 10" Long Each $0.06
$6.88
$2.99
431010 10FR, 10" Long 25/Case $1.24
$129.99
$61.99

More About Interglide Intermittent Catheter

Instructions For Using Intermittent Catheter:
  • Wash your hands thoroughly with soap and water. 
  • Remove catheter from the pack.
  • Position yourself comfortably, cleaning the opening of the urethra and surrounding area. 
  • Gently insert rounded end of catheter into urethra.
  • When urine stops flowing, remove catheter from urethra.
  • Dispose of catheter in accordance with local rules and regulations.
  • Wash your hands.
Warnings:  
  • Visually inspect the product for any imperfections or surface deterioration prior to use.
  • Some intermittent catheters may contain or have 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.
  • 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 failure, and/or to injury, illness or death of the patient

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