The recommended application sites are illustrated in the User Guide.
Applying the I-Port™ is simple and requires minimal training. Instructions can be found in the User Guide.
If applying the I-Port™ for the first time, perform the application in the presence of a healthcare professional.
Using the I-Port™ is simple and requires minimal training. Instructions can be found in the User Guide.
The I-Port™ is suitable for use on adults and children. Check with your healthcare professional to see if the I-Port™ is right for you.
Remove and replace the I-Port™ every 72 hours according to Centers for Disease Control guidelines or per your healthcare professional's instructions.
Yes, the I-Port™ is intended for use during normal daily activities, including showering, bathing or swimming.
The I-Port™ is 1½ inches (38mm) in diameter and rises only 1/3 inch (8.5mm) above the skin.
The cannula is the small soft, flexible tube used to deliver the medication into the subcutaneous tissue.
Yes, the soft, flexible cannula of the I-Port™ is available in two lengths for varying body types:
6 mm - Lean weight individuals
9 mm - Average to above average weight individuals
Talk to your healthcare professional about which cannula length is right for you.
The maximum needle length for use with the I-Port™ is 5/16 inch (8mm), a standard needle length for insulin syringes.
The thickest needle size for use with the I-Port™ is a 28 gauge needle.
The I-Port™ contains less than 0.005 mL of dead space (residual space), equivalent to 0.5 units of insulin.
No, the I-Port™ functions as a drug delivery channel directly into the subcutaneous tissue (the tissue layer located just beneath the skin). Visit the How it Works page to learn more.
The I-Port™ comes packaged in a box of 10 individually packaged devices, or roughly a one month supply.
Do not attempt to reuse the I-Port™ after the 72 hour wear period has elapsed. Do not attempt to reuse the I-Port™ after it has been removed or dislodged.
The discomfort associated with applying the I-Port™ is comparable to the discomfort associated with receiving an injection. Immediately after applying the device, you may feel the adhesive or cannula; however this feeling typically subsides quickly.
If discomfort remains for an extended period of time, remove the I-Port™ and replace with a new device. Should suggested actions not provide a resolution, contact your physician or healthcare professional.
Patton Medical Devices is currently exploring an auto-insertion device to be used with the I-Port™. Details regarding the availability of this product will be available soon.
Infection, irritation or inflammation from using the I-Port™ is rare, however the potential exists. Typically, these occurrences may result from inadequate cleansing of the skin surface before application, improper application to the body, and/or improper maintenance of the insertion site.
Remove and discard the I-Port™ and apply a new device to a different location on the body, at least 3 inches (76mm) from the original site. If infection, irritation or inflammation persists or worsens, discontinue use of the I-Port™ and contact your healthcare professional.
Remove and discard the I-Port™ and apply a new device to a different location on the body.
Test blood sugar per your healthcare professional's instructions to ensure that insulin dose and absorption at the delivery site are appropriate.
In the case of unexplainably high blood sugar, remove and discard the I-Port™ and apply new I-Port™ to a different location on the body since the cannula could be dislodged, crimped (bent) or partially clogged. If any of these instances occur, medication delivery may be limited. When using the I-Port™ to inject insulin, remember to test blood sugar 2 to 4 hours after use to ensure insulin performs as anticipated. Should suggested actions not provide a resolution to your high blood sugar, contact your healthcare professional.
Avoid applying and using a new I-Port™ just prior to bedtime, unless blood sugar can be checked 2 to 4 hours after injection.
Yes, insulin pens may be used with the I-Port™ as long as the needle length does not exceed 5/16 inch (8mm).
Speak with your healthcare professional to determine if the I-Port™ is right for you and to obtain a product sample.
The price of the I-Port™ is determined by the distributor and/or your health insurance plan. To find out if your health insurance plan will provide reimbursement for the I-Port™, fill out the I-Port™ Prescription Form, and have your doctor sign and fax the form into Patton Medical Devices at 866.286.1401. Our Customer Care team will contact you within 24 hours to discuss reimbursement and the next steps for obtaining the I-Port.
If your health insurance plan does not currently provide reimbursement for the I-Port™, please contact your plan administrator, healthcare professional and/or pharmacist to see if they can help us attain reimbursement for you.
After obtaining a prescription from your healthcare professional, you can purchase the I-Port™ through an authorized I-Port™ distributor. For more details about where you can purchase the I-Port™, please call our toll free number at 877-763-PORT to speak with a customer service representative.
If the I-Port™ packaging is damaged please call our toll free number at 877-763-PORT to speak with a customer service representative.
If the I-Port™ is damaged please call our toll free number at 877-763-PORT to speak with a customer service representative.
