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Powerflow™ Not Applicable PowerFlow™ IV Port Access Systems

PowerFlow™ IV Port Access Systems with 14 G BD lnsyte™ Autoguard™ Shielded IV Catheter

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Overview

PowerFlow™ IV Port Access Systems are convenient all-in-one kits designed specifically for the PowerFlow™ Implantable Apheresis IV Port. Kit components are organized to facilitate sterile “best practices” for PowerFlow™ IV Port access procedures, and to help clinicians comply with nursing society and CDC guidelines for sterile port access.

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Features and Benefits
Promotional Story
false
References

Please consult Instructions for Use for product indications for use, contraindications, warnings, precautions, complications, adverse events and detailed safety information.

true
Specification

GTIN - Box

20801741136638

10

GTIN - Case

10801741136631

5

GTIN - each

00801741136634

1


Quantity - Case

10/case

Minimum Order Quantity

1 case

GTIN

GTIN - Box 20801741136638 10
GTIN - Case 10801741136631 5
GTIN - each 00801741136634 1

Packaging

Quantity - Case 10/case
Minimum Order Quantity 1 case
References
false
Resources
References
false
Frequently Asked Questions
false
References
false
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
Recall Notifications
These recall notices provide current information on medical device recalls.
Learn more
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References
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