The features of BD Nexiva were designed by clinicians like you to meet your needs as you care for your patients. Every feature was designed with ease of use and enhanced clinical outcomes in mind. In addition, the BD Instafl ash Needle Technology is designed to reduce hit-and-miss insertion by confi rming vessel entry, enabling you to stay focused on the insertion site. Clinically-proven BD Vialon Biomaterial has longer indwell times and softens up to 70% in the vessel, reducing the chance of mechanical phlebitis by up to 50%
The only all-in-one PIVC shown to preserve sites for longer
Catalog No. | Color | Gauge | Catheter Length (in) | Catheter ID (mm) | Catheter OD (mm) | Gravity Flow Rate (mL/min) | Packaging |
383536 | Pink | 20 | 1.00 | 0.7874 – 0.8636 | 1.0668 – 1.1430 | 3660 | 20/Box 80/Case |
Integrated extension tubing and stabilization platform is designed to reduce manipulation and movement at the site and has been shown to reduce dislodgement and phlebitisby up to 50%.
Clinically demonstrated to reduce accidental dislodgement and complies with the Infusion Therapy Standards of Practice and CDC guidelines5Â for catheter stabilization.
98% reduced blood exposure during insertion due to the BD Nexiva IV catheter preassembled systems.
Proprietary BD Vialon biomaterial softens up to 70% in the vein, enabling longer dwell times and reducing the chance of mechanical phlebitis by up to 50%.
In a randomized study comparing the BD Nexiva IV catheter to an open catheter system, the median dwell time for BD Nexiva IV catheters was 144.5 hours and 96 hours for the open system.
By preserving sites for longer, the BD Nexiva IV catheter helps patients get the medication they need as scheduled, potentially decreasing their length of stay.
In a 2014 clinical study, the longer dwell time (6 days)Â of the BD Nexiva IV catheter led to cost reductions of approximately $1 million per year per 1000 beds compared with an open system.
What MRI safety information does the labeling contain? | Labeling does not contain MRI Safety Information |
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437): | No |
Device labeled as “Not made with natural rubber latex”: | No |
For Single-Use: | Yes |
Prescription Use (Rx): | Yes |
Over the Counter (OTC): | No |
Kit: | No |
Combination Product: | No |
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P): | No |
At Health Supply 770 Inc. speed is key. We take great pride in our ability to quickly prepare quotes, ship, and deliver high-quality medical equipment . Which makes us the ideal destination for all your medical needs.
Customer Service: 770-874-0431
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7111 Bayou George Dr. Panama City
Florida 32404