C.R. Bard 0600510 - PowerHohn Catheter without VitaCuff Antimicrobial Cuff, Single Lumen, 5 Fr, Basic Tray, Each

C.R. Bard 0600510 - PowerHohn Catheter without VitaCuff Antimicrobial Cuff, Single Lumen, 5 Fr, Basic Tray, Each

C.R. Bard 0600510 PowerHohn Catheter without VitaCuff Antimicrobial Cuff

he PowerHohn provides enhanced The PowerHohn provides enhanced over the wire placement due to catheter over the wire placement due to catheter design, construction and material. The PowerHohn catheters allow The PowerHohn catheters allow injection of contrast media for power injection computed tomography scans at a maximum of 5 cc/sec and a power injector alarm setting at a maximum of 300 psi.

The reverse taper hub gently plugs the The reverse taper hub gently plugs the insertion site and provides superior kink resistance PowerHohn catheters with the PowerHohn catheters with the VitaCuff Antimicrobial Cuff help reduce the possibility of infection in the tunnel tract PowerHohn catheters incorporate an PowerHohn catheters incorporate an exclusive bifurcation design and are clearly labeled to differentiate them from non-power injection catheters

• Power Injectable is printed on each extension leg for easy identification after catheter placement.
• Easily identifiable I.D. tags indicate maximum injection rate and prompts users to check catheter patency.
• Reverse taper hub gently plugs the insertion site and provides superior kink-resistance.
• All PowerHohn catheters are StatLock compatible.
• VitaCuff Antimicrobial Cuff discourages bacterial migration into the exit site and tunnel, and enhances catheter securement.
• PowerHohn catheters have depth markings every 1 cm on the catheter body

C.R. Bard 0600510 PowerHohn Catheter without VitaCuff Antimicrobial Cuff Basic Tray Contents

• Reverse Taper Polyurethane Radiopaque Catheter
• Dilator
• Guidewire
• Injection Cap(s)
• Needle, Introducer
• Scalpel
• Syringe
• Tunneler

Device Characteristics of C.R. Bard 0600510 PowerHohn Catheter without VitaCuff Antimicrobial Cuff

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":	Yes
For Single-Use:	Yes
Prescription Use (Rx):	Yes
Over the Counter (OTC):	No
Kit:	Yes
Combination Product:	No
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P):	No