Neonatal Monitoring Electrode, Pre-Wired with Soft Cloth, 0.9 inch × 0.9 inch
(2,2 cm × 2,2 cm) with 18 inch Metal Leadwires
Neonatal Monitoring Electrode, Pre-Wired with Soft Cloth, 0.9 inch × 0.9 inch
(2,2 cm × 2,2 cm) with 26 inch Radiolucent Leadwires
Neonatal, Pre-wired Limb Band Monitoring Electrode, 0.9 inch × 0.7 inch
(2,2 cm × 1,7 cm) with 18 inch Radiolucent Leadwires
Soft Cloth Monitoring Electrode 2.4 inch dia.
(6 cm dia.) with Solid Gel and Lift Tab
™
Micropore
Paper Tape Monitoring Electrode 2.4 inch dia.
(6 cm dia.) with Solid Gel, Abrader and Lift Tab
™
Micropore
Paper Tape Monitoring Electrode 1.75 inch dia.
(4,4 cm dia.) with Solid Gel and Lift Tab
Clear Tape Monitoring Electrode with Preattached Disposable Leadwire,
1 inch × 1.56 inch (2,5 cm × 4 cm) with 28 inch Radiolucent Leadwires
Clear Tape Monitoring Electrode with Preattached Disposable Leadwire,
1 inch × 1.56 inch (2,5 cm × 4 cm) with 48 inch Radiolucent Leadwires
Clear Tape Monitoring Electrode with Preattached Disposable Leadwire,
1 inch × 1.56 inch (2,5 cm × 4 cm) with 28 inch Radiolucent Leadwires
Diaphoretic Soft Cloth Monitoring Electrode 2.2 inch × 2 inch
(5,1 cm × 5,5 cm) with Solid Gel and Lift Tab
300 electrodes/case, 3/bag, 100 bags/case
300 electrodes/case, 3/bag, 100 bags/case
300 electrodes/case, 3/bag, 100 bags/case
1,000 electrodes/case, 50/bag, 20 bags/case
1,000 electrodes/case, 50/bag, 20 bags/case
1,000 electrodes/case, 50/bag, 20 bags/case
500 electrodes/case, 5/bag, 100 bags/case
500 electrodes/case, 5/bag, 100 bags/case
300 electrodes/case, 3/bag, 100 bags/case
1,000 electrodes/case, 50/bag, 20 bags/case
MRI Information
• This information is a consolidated summary of the MR conditions that are applicable to all the electrodes in the list.
For the conditions specic to each electrode, please refer to the product IFU.
• Disconnected 3M
in the MRI Safety Information labeling. Any deviation from those specic conditions may result in injury (e.g., burn) to the patient.
™
• 3M
MR Conditional electrodes have not been tested for MRI-related issues with any MR Conditional monitoring system. Therefore, the acceptable
use of 3M MR Conditional electrodes when connected to an MR Conditional monitoring system is unknown.
The information below pertains to the following 3M products:
Product Number Description
2244 3M™ Foam Monitoring Electrode
2268 3M™ Red Dot™ ECG Monitoring Electrode (2268-3, 2268-5)
2269T 3M™ Red Dot™ Neonatal, Pre-wired Monitoring Electrode
2570 3M™ Red Dot™ Monitoring Electrode with Foam Tape and Sticky Gel (2570, 2570-3, 2570-5)
2660 3M™ Red Dot™ Repositionable Monitoring Electrode (2660-3, 2660-5)
2670 3M™ Red Dot™ Repositionable Monitoring Electrode (2670-3, 2670-5)
2330 3M™ Red Dot™ Resting EKG Electrode
2360 3M™ Red Dot™ Resting EKG Electrode
Important Notes: 3M™ MR Conditional EKG/ECG Electrodes have not been tested for MRI-related issues with any MR Conditional monitoring system. Therefore, the acceptable use of 3M™ MR
Conditional EKG/ECG Electrodes when connected to an MR Conditional monitoring system is unknown. Disconnected 3M™ MR Conditional Electrodes can be worn safely during an MRI examination
according to the conditions of use presented in the MRI Safety Information labeling. Any deviation from those specic conditions may result in injury (e.g., burn) to the patient. It is unknown if this
3M Red Dot ECG electrode is acceptable for use with an MR conditional ECG monitoring system designed to be used to monitor a patient undergoing an MRI procedure.
™
MR Conditional electrodes can be safely worn by a patient during an MRI scan according to the conditions of use presented
MRI Safety Information
MR Conditional
The 3M™ Red Dot™ Cardiac Monitoring Electrodes (2244, 2268, 2269T, 2570, 2660 or 2670) or 3M™ Red Dot™ Resting Electrodes (2330 or
2360) were determined to be MR Conditional. Non-clinical testing demonstrated that the 3M Red Dot cardiac monitoring electrodes (2244,
2268, 2269T, 2570, 2660 or 2670) or 3M Red Dot resting electrodes (2330 or 2360) are MR Conditional. A patient with these electrodes
can be scanned safely immediately after placement under the following conditions:
• Static magnetic eld of 3-Tesla or less
• Maximum spatial gradient magnetic eld of 4,000-gauss/cm (40-T/m)
• Maximum MR system reported, whole body averaged specic absorption rate (SAR) of 4-W/kg
for 15 minutes of scanning (i.e., per pulse sequence) in the First Level Controlled Operating Mode
Under the scan conditions dened, the 3M EKG/ECG electrode is expected to produce a maximum temperature rise of 2.7°C after
15-minutes of continuous scanning (i.e., per pulse sequence). For 2269T, lead positioned in a straight conguration (i.e., no loops or cross
over points).
In non-clinical testing, the image artifact caused by the 3M EKG/ECG electrode extends approximately 5 mm from this device when imaged
using a gradient echo pulse sequence and a 3-Tesla MR system.
To learn more about 3M™ Red Dot™ Electrodes, call the 3M Health Care Helpline at
1-800-228-3957 or visit www.3M.com/RedDot
Medical Solutions Division
3M Health Care
2510 Conway Avenue
St. Paul, MN 55144-1000 USA
Phone 1-800-228-3957
Web 3M.com/RedDot
What is Alarm Fatigue?
go.3M.com/AlarmFatigue
Sign-up for the 3M Alarm Fatigue Reduction
Program: go.3M.com/AlarmFatigueProgram
How to Apply and Remove ECG Electrodes:
go.3M.com/RedDotHowTo
How to Troubleshoot ECG Artifacts:
go.3M.com/TroubleshootingECGArtifacts