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PureWick™ External catheters PureWick™ Female External Catheter

PureWick™ Female External Catheter Kit

Intended for non-invasive urine output management in female patients. Not made with natural rubber latex.

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1.770.784.6100
bardmedical.customerservice@crbard.com
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8195 Industrial Boulevard Covington, Georgia 30014 United States
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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
  • CAUTI Risk
    Helps reduce urinary catheter days, lowering CAUTI risk
  • Non-Invasive
    Non invasive urine output management
  • Protects Skin
    Protects skin by wicking away urine
  • CAUTI Risk
    Helps reduce urinary catheter days, lowering CAUTI risk
  • Non-Invasive
    Non invasive urine output management
  • Protects Skin
    Protects skin by wicking away urine
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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 - Each

00801741183614

1

GTIN - Box

20801741183618

180

GTIN - Case

10801741183611

30

Latex Statement

Not made with natural rubber latex

Quantity - Case

30/Cs

Packaged with

PureWick™ Female External Catheter, peri-care wipes, duration label

GTIN

GTIN - Each 00801741183614 1
GTIN - Box 20801741183618 180
GTIN - Case 10801741183611 30

FDA, Premarket Approval, and Regulatory

Latex Statement Not made with natural rubber latex

Packaging

Quantity - Case 30/Cs
Packaged with PureWick™ Female External Catheter, peri-care wipes, duration label
References
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Electronic Instructions for Use (eIFUs)
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Product Complaints
North American Regional Complaint Center
1-844-8BD-LIFE (1-844-823-5433)
productcomplaints@bd.com
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
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