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General| Device Type | Insertable Cardiac Monitor (ICM) |
|---|---|
| Communication | Wireless telemetry |
| Implantation Depth | Subcutaneous |
| Sensing Method | Single-lead ECG sensing |
| Weight | 2.4 grams |
| Battery Life | Approximately 3 years |
| Data Storage | 30 minutes of ECG data |
| MRI Compatibility | MR Conditional |
| Size | Approximately 1 cubic centimeter |
| Connectivity | Wireless connectivity with CareLink network |
| Indication | Monitoring for cardiac arrhythmias |
| Compatibility | Compatible with Medtronic CareLink Network |
| Detection Capabilities | Atrial fibrillation, bradycardia, tachycardia |
| Data Transmission | Automatic and manual data transmission |
Conformité Européenne (European Conformity). This symbol means that the device fully complies with European Union Acts.
Explains the Medtronic Reveal LINQ system, its components, and how it records heart activity for diagnosis.
Details the Reveal LINQ cardiac monitor, its insertion, function, and ECG recording methods.
Describes the Patient Assistant model PA96000 for recording symptoms and its use with the cardiac monitor.
Explains the MyCareLink Patient Monitor for transmitting recorded data to the clinic.
States that there are no known contraindications for the use of this device.
Provides answers to common questions from new patients. Contact doctor for more questions.
Details the simple procedure for implanting the cardiac monitor, taking 15-20 minutes.
Warns about risks like swelling, warmth, drainage, or fever, and the potential for infection.
Explains scheduling of follow-up appointments, which can be in-clinic or remote.
Describes using CareLink Service and MyCareLink for remote data transmission to the clinic.
Details screens displayed on the MyCareLink Patient Monitor and actions required for Reveal LINQ.
Provides an overview of items that may temporarily interfere with data collection capabilities.
Outlines precautions to be taken regarding certain types of medical procedures.
Explains which household electrical items can affect the data stored in the cardiac monitor.
Lists wireless communication devices that can affect the cardiac monitor and required distances.
Details household and hobby items with motors that can cause EMI and required distances.
Discusses home power tools and their potential effects, providing minimum distances for interference avoidance.
Lists industrial equipment that may cause EMI and require avoidance or precautions.
Determines safe distances between radio transmitter antennas and cardiac monitors.
Provides precautions for passing through electronic antitheft and airport security systems.
Warns to inform doctors before medical procedures and lists procedures requiring precautions.
Details Industry Canada compliance requirements for the device.
States that the product conforms with essential requirements of Directive 1999/5/EC.
