User Guide

Directions
Open the MedLite ID peel pack and remove the three devices
from the pack.
Prior to connecting the primary medication line to patient,
apply a MedLite ID device below the drip chamber, at the primary
medication injection site and near attachment of the venous
access catheter (see figure) by running the infusion tubing
through the tubing grooves on the device.
Inspect tubing for twists or kinks, then close the clamshell
door until it clicks.
The MedLite ID device has two forms of identification for the
medication line, the attached device itself and an activated
light as well.
To activate, press one of the attached devices on the circular
squeeze point. This will activate the lights for all three devices
within a given set. The devices will turn off after about 45 seconds.
Pressing on any of the devices will turn all devices back on.
The devices are for one infusion set use and should be disposed
of when tubing is changed or treatment completed.
Warning and Disclaimer
This device should be installed by a medical professional. Do not use any component of the device if the
product packaging is damaged or opened. MedLite ID is not responsible for use of the product taken
from deteriorated packaging or used on non-medication intravenous lines. MedLite, ID is a single use
device with multiple components. Never reuse any portion of the device, even if the device appears
undamaged. All portions of the device should be discarded when tubing is changed, or the treatment
completed. Care must be taken after opening the device to protect from damage to the components.
Prior to installation, all portions of the device must be verified to be in good working order.
If any portion of these instructions are disregarded, the medical professional and their respective
employers, agents, members, managers, partners, officers, affiliates, parent entities, assigns, and all other
persons or entities who may be responsible for the disregard assume the risk of the use of the product.
Changes or modification to this unit not expressly approved by the party responsible for compliance
could void the user’s authority to operate the equipment.
By using this product, it is presumed that this warning and disclaimer has been read and understood.
For further information or to share comments or complaints about this product, please visit
www.medliteid.com.
RF Exposure Information
This equipment complies with FCC/ISED radiation exposure limits set forth for an uncontrolled
environment. In order to avoid the possibility of exceeding the FCC/ISED radio frequency exposure limits,
human proximity to the antenna shall not be less than 20 cm during normal operation.
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FOR PATIENT SAFETY this product is
intended for use with primary medication line only.
Warning !
Warning !
Patents: medliteid.com/patents
Attach MedLite ID to primary medication
line prior to connecting IV to patient.
To prevent reduced or obstructed infusion
set flow, be sure that when closing the
MedLite ID clamshell over the primary
medication line that the tubing is not
pinched or twisted.
This device complies with Part 15 of the FCC Rules and this device also contains
licence-exempt transmitter(s)/receiver(s) that comply with Innovation,Science and Economic
Development Canada’s licence-exempt RSS(s). Operation is subject to the following two
conditions: (1)this device may not cause harmful interference, and (2) this device must
accept any interference received, including interference that maycause undesired operation.
Contact: US www.medliteid.com
EU www.medliteid.com
FCC ID: 2ATMC-IDAO1US
IC: 26774-IDA01US
HVIN: IDA01US
IFU: 02.25.2021 - v7.9