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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PowerFlow™
PowerFlow™ IV Port Access Systems
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PowerFlow™ IV Port Access Systems with 14 G BD lnsyte™ Autoguard™ Shielded IV Catheter
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1.844.8.BD.LIFE (1.844.823.5433)
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1.844.8.BD.LIFE (1.844.823.5433)
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850 W Rio Salado Pkwy, Tempe, AZ 85281 United States
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1.844.8.BD.LIFE (1.844.823.5433)
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1.800.440.5376
- Overview
- Specifications
- eIFUs and Resources
- FAQ
- Product Notifications
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FEATURE AND BENEFIT CARDS NOT AVAILABLE
FEATURE AND BENEFIT CARDS NOT AVAILABLE
false
Please consult Instructions for Use for product indications for use, contraindications, warnings, precautions, complications, adverse events and detailed safety information.
true
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 |
false
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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
Recall Notifications
These recall notices provide current information on medical device recalls.
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