{"AlternateComparison":true,"RelatedProducts":false,"Specification":true,"FeatureBenefit":false}
GuardIVa™ Port Access Kits with GuardIVa™ Antimicrobial Hemostatic IV Dressing

MiniLoc® Safety Infusion Set PAK + GuardIVa® Dressing with Y-Injection Site, 22 G x 1.5 in

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1.714.283.2228
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1.714.283.8424
oem@carefusion.com
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1.844.8.BD.LIFE (1.844.823.5433)
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1.800.847.2220
Overview
  • Designed to standardize port access procedures
  • Provides the convenience of necessary kit components in a common package
  • Kit components are organized to facilitate sterile “best practices” for port access related procedures
  • Assists clinicians in complying with guidelines for sterile port access outlined by nursing societies and the CDC
  • Procedural Checklist included in every kit:
    • Educate and assist in sterile port access technique
    • Convenient documentation and tracking of port access procedure
    • Procedural checklist for simplified protocol documentation

The GuardIVa® dressing significantly lowered re-growth of skin microflora at day 7 and day 10 compared to the control.1

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Features and Benefits
Promotional Story
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References

1. As demonstrated through in vivo testing. Data on file.

Vescia, S. et al., Management of Venous Port Systems in Oncology: A review of current evidence, Annals of Oncology, Sept 2007, 19:9-15.

Groeger, Jeffrey S. et.al., Infectious Morbidity Associated with Long-Term Use of Venouos Access Devices in Patients with Cancer, Annals of Internal Medicine, 1993; 119:1168-1174.

Grannan, Kevin I., et.al., Early and Late Complications of Totally Implantable Venous Access Devices, Journal of Surgical Oncology, 1990, 44:52-54.

Pegeus, David, et.al., Comparison of Infections in Hickman and Implanted Port Catheters in Adult Solid Tumor Patients, Journal of Surgical Oncology, 49: 156-162 (1992). Groeger, Jeffrey S. et.al., Venous Access in the Cancer Patient, Principles and Practice of Oncology, 1991; vol. 5 no. 3

† Survey results on file at C. R. Bard, Inc.

Please go to the product specific page to find the Safety Information link for inserts and labels, as well as indications, directions for use, contraindications, hazards, warnings, and precautions.

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Specification

GTIN - Case

10801741095846

5

GTIN - each

00801741095849

1


Gauge Size

22 Ga

Length

1.5"

With Y-Site Product Code

with Y-Injection Site

GTIN

GTIN - Case 10801741095846 5
GTIN - each 00801741095849 1

Product Basic Specification

Gauge Size 22 Ga
Length 1.5"
With Y-Site Product Code with Y-Injection Site
References
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Resources
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Frequently Asked Questions
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References
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Alternatives Comparison
  • Alternatives Comparison

    • Product Name
    • Gauge Size
    • Length
    • With Y-Site Product Code
    • Product Name
    • Gauge Size
    • Length
    • With Y-Site Product Code
    • Product Name
    • Gauge Size
    • Length
    • With Y-Site Product Code
    • Product Name
    • Gauge Size
    • Length
    • With Y-Site Product Code
    • Product Name
    • Gauge Size
    • Length
    • With Y-Site Product Code
    • Product Name
    • Gauge Size
    • Length
    • With Y-Site Product Code
  • Product Image
    • Product Name

      MiniLoc® Safety Infusion Set PAK + GuardIVa® Dressing with Y-Injection Site, 22 G x 1.5 in
    • Gauge Size

      22 Ga
    • Length

      1.5"
    • With Y-Site Product Code

      with Y-Injection Site
  • Product Image
    • Product Name

      MiniLoc® Safety Infusion Set PAK + GuardIVa® Dressing, 22 G x 1.5 in
    • Gauge Size

      22 Ga
    • Length

      1.5"
    • With Y-Site Product Code

      without Y-Injection Site
Related Products
RELATED PRODUCTS NOT AVAILABLE
References
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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