PowerPort® isp M.R.I.® Implantable Port
- Cosmetically appealing with compact size
- Lightweight for patient comfort
- Radio-translucent
- Reduced artifact
- Enables superior imaging
- Easily identifiable
- Power injectable
- Plastic port body
Available sizes:6 Fr. & 8 Fr. Polyurethane Catheter, 8 Fr. Groshong Catheter and 9.6 Fr. Silicone Catheter
Features
Feel and See the Standard of Care®
The PowerPort® isp M.R.I.® device provides the benefits of power injection (when used with the PowerLoc® Safety Infusion Set Family† device) with the ability to see through the port with minimal artifact. The PowerPort® isp M.R.I.® device is radio-translucent and allows patients to receive IV therapies and CECT scans without the need for repeated needlesticks.
It combines reliable venous access with the unique ability for power-injected Contrast-Enhanced Computed Tomography (CECT) scans. Power-injected CECT scans produce superior images to help better manage patient care. Such scans are often used to track tumor markers or perform pulmonary embolism studies.
Benefits of the PowerPort® isp M.R.I.® Implantable Port Device
Polyurethane 6 Fr. & 8 Fr. Catheter
Taxol™/Taxotere™ drug resistant
Cosmetically appealing with compact size
Lightweight for patient comfort
Radio-translucent ability to see through the port
Reduced artifact better imaging capability
Unique Patient Discharge Packet
The palpation bumps and unique triangular shape of PowerPort® Implantable Ports make them easily distinguishable from non-power ports. PowerPort® devices offer easy, flexible placement and access.
- Suture Plugs (open or silicone-filled options available)
- Unique triangular
port shape - Soft palpation bumps
on septum
Enables Superior Imaging
Power Injection and CECT Scan Compatible when used with PowerLoc® Safety Infusion Set
Indicated for power injection of contrast media up to 5 mL/sec
Power Injected CECT Scans Produce Superior Images to help better-manage patient care
Click here to view MR Conditional Statement
Radiopaque identifier on the bottom of the port to aid in:
- Identification of the PowerPort® device under X-ray
- Identification of a flipped port under X-ray
(Roll over image to view X-ray)
Enables Reliable Venous Access
Receive IV therapies
Reduce repeated needle sticks
Receive contrast-enhanced CT scans
Easy, flexible placement and access
The PowerLoc® safety infusion set is the ideal device for accesing PowerPort® devices. This combination of power injectable devices enables contrast agents to be power-injected. As a result, tissues show up more clearly in CECT scans, making it easier to monitor patient condition.
A variety of PowerLoc® safety infusion set options are also available as accessory kits for continued PowerPort® device access needs.
Power Injectable
300 psi, 19 gauge and 20 gauge needles with 5 mL/s maximum infusion rate
300 psi, 22 gauge needle with 2 mL/s maximum infusion rate
Comfortable for the Patient
Small foot print
Easy to dress
Ultra low profile
Lower insertion and penetration force than other non-siliconized port access needles
This product does not contain DEHP
This product does not contain natural rubber latex
† E.g. PowerLoc®, PowerLoc® Max safety infusion set.
Please consult product labels, IFU, and package inserts for any indications, contraindications, hazards, warnings, cautions, and instructions for use.
Comparison
Feel and See the Standard of Care®
The palpation bumps and unique triangular shape of PowerPort® Implantable ports make them easily distinguishable from non-power ports. The PowerPort® devices offer easy, flexible placement and access.
| PowerPort® Slim Device | PowerPort® Ti isp Device | PowerPort® MRI® isp Device | PowerPort® Ti Device | PowerPort® MRI® Device | PowerPort® Duo Device | PowerPort® Alternative Bump Device | |
|---|---|---|---|---|---|---|---|
| MRI Conditional | • | • | • | • | • | • | • |
| Titanium Port Body | • | • | • | • | |||
| Plastic Port Body | • | • | • | • | |||
| Single Lumen | • | • | • | • | • | • | |
| Dual Lumen | • | ||||||
| 6 Fr. (Pu) | • | • | • | • | |||
| 8 Fr. (Pu) | • | • | • | • | • | ||
| 8 Fr. Groshong® Catheter (Heparin Opt) | • | • | • | • | • | • | |
| 9.6 Fr. (Si) | • | • | • | ||||
| 9.5 Fr Dual Catheter (Pu) | • | ||||||
| Silicone Filled Suture Holes | • | • | • | • | • | • | • |
| Open (non-silicone filled ) Suture Holes | • | • | • | • | • | • |
• = Yes
• = Either/Or
(Pu) = Polyurethane Catheter
(Si) = Silicone Catheter
Specifications
| Product Code | Code Description | Suture Plugs | Kit Type |
|---|---|---|---|
| 4808060 | PowerPort® isp M.R.I.® device with 8.0 Fr, Attachable Polyurethane Catheter, and Alternative Bumps | Silicone Filled | Intermediate |
| 4808061 | PowerPort® isp M.R.I.® device with 8.0 Fr, Attachable Polyurethane Catheter, and Alternative Bumps | Open (Non-Silicone Filled) | Intermediate | 1806060 | PowerPort® isp M.R.I.® device with 6.0 Fr Attachable Polyurethane Catheter | Silicone Filled | Intermediate |
| 1806061 | PowerPort® isp M.R.I.® device with 6.0 Fr Attachable Polyurethane Catheter | Open (Non-Silicone Filled) | Intermediate |
| 1806050 | PowerPort® isp M.R.I.® device with 6.0 Fr Attachable Polyurethane Catheter | Silicone Filled | Microintroducer |
| 1806051 | PowerPort® isp M.R.I.® device with 6.0 Fr Attachable Polyurethane Catheter | Open (Non-Silicone Filled) | Microintroducer |
| 1808060 | PowerPort® isp M.R.I.® device with 8.0 Fr Attachable Polyurethane Catheter | Silicone Filled | Intermediate |
| 1808061 | PowerPort® isp M.R.I.® device with 8.0 Fr Attachable Polyurethane Catheter | Open (Non-Silicone Filled) | Intermediate |
| 1808050 | PowerPort® isp M.R.I.® device with 8.0 Fr Attachable Polyurethane Catheter | Silicone Filled | Microintroducer |
| 1808051 | PowerPort® isp M.R.I.® device with 8.0 Fr Attachable Polyurethane Catheter | Open (Non-Silicone Filled) | Microintroducer | 4808560 | PowerPort® isp M.R.I.® device with 8.0 Fr, Attachable Groshong® Catheter, and Alternative Bumps | Silicone Filled | Intermediate |
| 4808561 | PowerPort® isp M.R.I.® device with 8.0 Fr, Attachable Groshong® Catheter, and Alternative Bumps | Open (Non-Silicone Filled) | Intermediate |
| 1808560 | PowerPort® isp M.R.I.® device with 8.0 Fr Attachable Groshong® Catheter | Silicone Filled | Intermediate |
| 1808561 | PowerPort® isp M.R.I.® device with 8.0 Fr Attachable Groshong® Catheter | Open (Non-Silicone Filled) | Intermediate |
| 1808550 | PowerPort® isp M.R.I.® device with 8.0 Fr Attachable Groshong® Catheter | Silicone Filled | Microintroducer |
| 1808551 | PowerPort® isp M.R.I.® device with 8.0 Fr Attachable Groshong® Catheter | Open (Non-Silicone Filled) | Microintroducer |
| 1809660 | PowerPort® isp M.R.I.® device with 9.6 Fr Attachable Silicone Catheter | Silicone Filled | Intermediate |
| 1809661 | PowerPort® isp M.R.I.® device with 9.6 Fr Attachable Silicone Catheter | Open (Non-Silicone Filled) | Intermediate |
| 1859660 | PowerPort® isp M.R.I.® device with 9.6 Fr Pre-Attached Silicone Catheter | Silicone Filled | Intermediate |
| 1859661 | PowerPort® isp M.R.I.® device with 9.6 Fr Pre-Attached Silicone Catheter | Open (Non-Silicone Filled) | Intermediate |
ChronoFlex* Polyurethane Catheters
ChronoFlex* polyurethane catheters have been proven to exhibit superior biodurability compared with other polyurethane catheters, making them ideal for long-term, blood-contacting devices. In vivo studies indicate the ChronoFlex* polyurethane catheter has less propensity for surface biodegradation, making it more resistant to environmental stress cracking.
- Given the inherent material strength of ChronoFlex* polyurethane, it is superior to Tecoflex* urethane for use with Taxol* or Taxotere* drugs.
- Firmness and rounded tip facilitate advancement into vein.
- Thin catheter walls offer increased flow-rate capabilities.
- ChronoFlex* polyurethane catheters are exclusive to Bard Access Systems’ implanted ports.
Groshong* Catheters
The three-way Groshong* valve allows infusion and blood aspiration while reducing the risk of air embolism, blood reflux and clotting. Flushing frequency is decreased because the valve prevents blood from backing into the catheter and clotting. Because the system is closed, routine maintenance is simplified and the need for heparin is eliminated.
- Negative pressure opens valve inward, permitting blood aspiration.
- Positive pressure opens valve outward, allowing infusion.
- At neutral pressure, valve remains closed, reducing risk of air embolism, blood reflux and clotting.
Open-Ended Silicone Catheters
Bard Access Systems’ open-ended central venous catheters continue to set the standard for performance and reliability.
- Soft, atraumatic tip offers added safety during implantation.
- Medical-grade radiopaque silicone construction ensures biocompatibility.
- Available in attachable and pre-attached configurations.
Literature
Please refer below to the Instructions for Use (IFUs) for any indications, contraindications, hazards, warnings, and cautions.