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

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

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DuoGlide™ Short-Term Dialysis Catheter

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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
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Features and Benefits
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Specification

GTIN - Box

20801741042083

50

GTIN - Case

10801741042086

5

GTIN - Each

00801741042089

1


Kit Configuration

Kit

Package

5/shelfpack, 50/case


Catheter Size

13.0 Fr

Insertion Length (Tip to Cuff)

24 cm

Catheter Configuration

Curved Extension Leg

GTIN

GTIN - Box 20801741042083 50
GTIN - Case 10801741042086 5
GTIN - Each 00801741042089 1

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 Curved Extension Leg
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Electronic Instructions for Use (eIFUs)
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Frequently Asked Questions

Catheter Indications and Materials

The DuoGlide Catheters are indicated for use in attaining short-term (less than 30 days) vascular access for hemodialysis, hemoperfusion, and apheresis therapy via the jugular, subclavian or femoral vein.

The catheter is intended for short-term vascular access only and is not to be used for any purpose other than indicated.

 

Catheter Performance

The DuoGlide Catheter flows at 400 mL/min for all lengths with low arterial/venous pressures (less than 250 mmHg). As suggested by in vitro data using a blood simulate approximating the viscosity of whole blood.

The rate of recirculation of the dialysis lumens is less than 1% on average in both the forward and reverse directions when tested in vitro1 at a flow rate of 300 mL/min with the symmetrical tip design of the 24 cm DuoGlide Short Term Dialysis Catheter. Note that recirculation in femoral catheters is likely significantly greater than in internal jugular placed catheters.2

Bench test results may not necessarily be indicative of clinical performance.

 

Catheter and Kit Options

The DuoGlide Catheter outer diameter is 13 French. The intra lumens are large 12 gauge lumens that allow for flows of 400 mL/min.

The DuoGlide Catheter is available in both straight and curved extension leg configurations.

The DuoGlide Catheter is available in 12.5 cm (curved extension configuration only), 15 cm, 20 cm, 24 cm, and 30 cm (straight extension configuration only).

Transparent, rotatable wing allows for easy visualization and cleaning of exit site.

 

Placement, Maintenance and Care

The DuoGlide Catheter is intended to be inserted in the jugular, femoral, or subclavian vein as required.

WARNING: The catheter must not be left in the femoral vein longer than three days.

The DuoGlide Dialysis Catheter is compatible with the following agents: Povidone iodine, 0.55% sodium hypochlorite solution, chlorhexidine gluconate 4%, chlorhexidine gluconate 2% solution, dilute aqueous sodium hypochlorite, hydrogen peroxide, bacitracin zinc ointments in petrolatum bases.

WARNING: Acetone and PEG-containing ointments can cause failure of this device and should not be used with polyurethane catheters. Chlorhexidine patches or bacitracin zinc ointments are the preferred alternatives.

Yes, the DuoGlide Catheter may be exchanged over a guidewire. The wire included in the kit is a 0.035 inch wire which fits through the venous lumen of the catheter.

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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
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