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PowerGlide Pro™ Midline Catheter

Cue™ Needle Tracking System 20 G, 10 cm, Basic

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Ordering
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1.714.283.2228
5 a.m. to 4 p.m. PT
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1.714.283.8424
oem@carefusion.com
Customer Service
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1.844.8.BD.LIFE (1.844.823.5433)
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1.800.847.2220
Overview

Empowering Nurses to Put Patients First

Designed to help increase both patient and clinician satisfaction.

The PowerGlide Pro™ Midline Catheter:

  • Allows catheter dwell time for up to 29 days, reducing the need for multiple peripheral IVs
  • Supplies a guidewire designed to assist with insertion success
  • Offers a longer, body-softening polyurethane catheter to help minimize vessel wall trauma
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Features and Benefits
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References

* F2XXXX1 and M000001 trays do not contain a GuardIVa® Antimicrobial Hemostatic IV Dressing.

1. Compared to the similar non-reinforced tip catheters. All data on file at Bard. Bench test results may not be predictive of clinical performance.

*Depending on the kit ordered, these components will differ.

Please consult product labels, IFU, and package inserts for any indications, contraindications, hazards, warnings, cautions, and instructions for use.

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Specification

GTIN - each

00801741152474

1

GTIN - Box

20801741152478

10

GTIN - Case

10801741152471

5


Quantity

20/case


Gauge Size

20 Ga

Length

10 cm

Power Injection Flow Rate

5 mL/sec

Type

Basic

GTIN

GTIN - each 00801741152474 1
GTIN - Box 20801741152478 10
GTIN - Case 10801741152471 5

Packaging

Quantity 20/case

Product Basic Specification

Gauge Size 20 Ga
Length 10 cm
Power Injection Flow Rate 5 mL/sec
Type Basic
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Frequently Asked Questions
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Related Products
RELATED PRODUCTS NOT AVAILABLE
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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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