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Ureteral catheters Dual lumen ureteral catheter

Ureteral Catheters, Dual Lumen

Does not contain natural 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 Dual Lumen Ureteral Catheter is a radiopaque catheter that is temporarily and transurethrally placed in the renal pelvis and ureter. It is used for urethral catheterization, collecting specimen, pyelography drug infusion, and dilation of ureteral strictures. The ureteral catheter should be inserted into the ureter using standard endourologic technique, under direct fluoroscopic or radiographic visualization. 

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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

00801741052903

1


Quantity

1 each


Size

Guidewire Comp: 0.038, Length 50cm, 10FR

GTIN

GTIN - Each 00801741052903 1

Packaging

Quantity 1 each

Product Basic Specification

Size Guidewire Comp: 0.038, Length 50cm, 10FR
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Electronic Instructions for Use (eIFUs)
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Frequently Asked Questions
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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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