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DuoGlide™ Acute dialysis catheters DuoGlide™ Short-Term Dialysis Catheter

DuoGlide™ Short-Term Straight Dialysis Catheter Kit 13 Fr Basic Kit (dual lumen) 24 cm insertion length

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1.844.8.BD.LIFE (1.844.823.5433)
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DuoGlide™ Short-Term Dialysis Catheter

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Customer Service
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1.844.8.BD.LIFE (1.844.823.5433)
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1.800.847.2220
OEM@bd.com
Overview
  • Dual lumen
  • Kink-resistant catheter design
  • Symmetrical tip
  • Catheter length options
  • Maximal barrier trays
  • Straight or curved extension legs
true
Features and Benefits
Promotional Story
false
References
false
Specification

GTIN - Box

20801741042038

50

GTIN - Each

00801741042034

1

GTIN - Case

10801741042031

5


Kit Configuration

Kit

Package

5/shelfpack, 50/case


Catheter Size

13.0 Fr

Insertion Length (Tip to Cuff)

24 cm

Catheter Configuration

Straight

GTIN

GTIN - Box 20801741042038 50
GTIN - Each 00801741042034 1
GTIN - Case 10801741042031 5

Packaging

Kit Configuration Kit
Package 5/shelfpack, 50/case

Product Basic Specification

Catheter Size 13.0 Fr
Insertion Length (Tip to Cuff) 24 cm
Catheter Configuration Straight
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Electronic Instructions for Use (eIFUs)
Resources
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false
Frequently Asked Questions
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false
Related Products
RELATED PRODUCTS NOT AVAILABLE
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false
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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