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PureWick™ External catheters PureWick™ Female External Catheter

PureWick™ Female External Catheter

Non-invasive urine output management in female patients. Not made with natural rubber latex.

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1.844.8.BD.LIFE (1.844.823.5433)
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1.770.784.6100
bardmedical.customerservice@crbard.com
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8195 Industrial Boulevard Covington, Georgia 30014 United States
Customer Service
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1.844.8.BD.LIFE (1.844.823.5433)
bardmedical.customerservice@crbard.com
Overview

The PureWick™ Female External Catheter is intended for non-invasive urine output management in female patients. Using low pressure wall suction, the PureWick™ Female External Catheter wicks voided urine away from the patient and into a designated collection canister.

The #1 CAUTI risk factor is prolonged catheterization.1,2 The risk of infection increases every day a catheter is indwelling. The #2 CAUTI risk is female gender and over half of hospital in-patients are females who are at a 3x higher risk for developing a CAUTI and 61% more likely to be catheterized.1,3

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Features and Benefits
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References

Specifications subject to change without notice.

For the latest information, always check the “Instructions for Use” that comes packaged with the product. If you are a consumer seeking more information, please consult your healthcare provider.

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Specification

GTIN - Case

10801741163088

30

GTIN - Box

20801741163085

180

GTIN - Each

00801741163081

1


Quantity - Case

30/Cs

GTIN

GTIN - Case 10801741163088 30
GTIN - Box 20801741163085 180
GTIN - Each 00801741163081 1

Packaging

Quantity - Case 30/Cs
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Electronic Instructions for Use (eIFUs)
Resources
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false
Frequently Asked Questions
false
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false
Related Products
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Product Complaints
North American Regional Complaint Center
1-844-8BD-LIFE (1-844-823-5433)
Things to Consider

If you are a patient or end user, you can contact us yourself, or you may have your caregiver or your physician do that for you. To help us process your
information quickly and effectively, please contact our customer complaints
team.

To better facilitate our investigation, please include the following information in your reporting:


  • Product Name and/or Catalog Number
  • Lot Number or Serial Number
  • Any injuries and/or Harm?
  • What is the issue you experienced?
  • Is the actual sample or sample representative available? (If possible, please send affected sample)
  • Contact name and phone number
Product Recalls
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Recall Notifications
These recall notices provide current information on medical device recalls.
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