User's Manual
Table Of Contents
- general description
- Description
- Indications for Use
- Intended Use
- Contraindications
- Programmer Warnings and Cautions
- General
- Electrostatic Discharge (ESD)
- S-ICD System Warnings and Cautions
- General
- Use of Other Medical Therapies/Diagnostic Procedures
- Electromagnetic Interference (EMI) Outside the Hospital Environment
- S-ICD System Clinical Investigation
- Potential Adverse Events
- Setup of the Q-TECH Programmer
- Packaging
- Programmer Controls and Connections
- Charging the Programmer
- Using the Q-TECH Programmer
- Turning the Programmer On
- Changing the Programmer Volume Level
- Placing the Programmer in Suspend Mode
- Turning the Programmer Off
- Using the Programmer Touch Screen
- Using the Wand
- Navigation
- Screen Header
- Navigation Bar
- Restarting the Programmer
- Configuring the Q-TECH Programmer
- Configuring Programmer Settings
- Date and Time Format
- Time Zone
- Language Preference
- Printer Selection
- Programmer Software Version
- Modes of Operation for the Q-TECH Programmer
- Online Behavior
- Offline Behavior
- Modes of Operation for the SQ-RX Device
- Shelf Mode
- Therapy On Mode
- Therapy Off Mode
- Connecting and Disconnecting from the SQ-RX Device
- Scanning For SQ-RX Devices
- Connecting to the SQ-RX Device
- Connecting to an SQ-RX Device in Shelf Mode:
- Ending a Patient Session
- Programming the SQ-RX Device at Implant
- Entering Electrode Information
- Creating the Patient Chart
- Automatic Setup
- Programming Therapy Parameters
- Defibrillation Testing
- Performing an SQ-RX Follow-up
- Sensing Configuration and Automatic Setup
- Viewing SQ-RX Device Status
- Viewing Stored Episodes
- Printing Reports from the Programmer
- Printing Reports
- Summary Report
- Captured S-ECG Report
- Episodes Report
- S-ECG Features
- S-ECG Rhythm Strip Markers
- S-ECG Scale Settings
- Capture and View S-ECG Strips
- Utilities Menu
- Acquire Reference S-ECG
- Capture All Sense Vectors
- Beeper Control
- Manual Setup
- Smart Charge
- Additional Programmer Functions
- Rescue Shock
- Manual shock
- S-ICD System Magnet Model 4520
- Charging the Programmer
- Cleaning the Programmer
- Service
- Maintenance Check
- Safety Measurements
- Programmer End of Life
- Inability to Print
- No Printer Available
- Touch Screen Inactive while Connected to AC Power
- Loss of Communication with Printer
- Inability to Communicate With the SQ-RX Device
- Federal Communications Commission (FCC) US
- Essential Performance
- EMI/RFI
- Declarations tables
- Table 3: Declaration Electromagnetic Emission
- Table 4: Declaration Electromagnetic Immunity Part 1
- Table 5: Declaration Electromagnetic Immunity Part 2
- Table 6: Recommended Separation Distances
- Table 7: EMI/RFI Information: Programmer–to–pulse generator
- Table 8: EMI/RFI Information: Programmer–to–printer (Bluetooth®)
- Specifications
- Table 9: Product Guidelines
- Table 10: Specifications
- Table 11: Nominal Specifications
- Definition of package label symbols
- Table 12: Packaging Symbols: Q-TECH Programmer
- Table 13: Packaging Symbols: Q-TECH Programmer Wand
- Warranty
- Limited Warranty
1
QTECH™ PROGRAMMER: GENERAL DESCRIPTION
Description
The Q-TECH Programmer (the “programmer”), Model 3200, is a component of the Cameron Health/
Boston Scientic S-ICD System, which is prescribed for patients when cardiac arrhythmia management
is warranted. The other components of the S-ICD System include the SQ-RX Pulse Generator (the “SQ-
RX device”), Q-TRAK Subcutaneous Electrode (“electrode”) and the Q-GUIDE Subcutaneous Electrode
Insertion Tool (“EIT”).
The programmer is a non–sterile, non–implantable, tablet computer controlled by a graphic user
interface (GUI) displayed on a touchscreen. The programmer is powered by either AC line power
or an internal lithium ion battery pack. The programmer uses a connected RF telemetry wand to
communicate wirelessly with the SQ-RX device to enable adjustment of programmable settings as well
as collection of data.
The S-ICD System is designed for ease of use and simplicity of patient management. The S-ICD System
has a number of automatic functions designed to reduce the amount of time required for implantation,
initial programming and patient follow-up.
Indications for Use
The S-ICD System is intended to provide debrillation therapy for the treatment of life-threatening
ventricular tachyarrhythmias in patients who do not have symptomatic bradycardia, incessant
ventricular tachycardia, or spontaneous, frequently recurring ventricular tachycardia that is reliably
terminated with anti-tachycardia pacing.
Intended Use
The programmer is intended to communicate with the SQ-RX device. The programmer software controls
all SQ-RX device communication functions.
Contraindications
Unipolar pacemakers are contraindicated for use with the S-ICD System.
Programmer Warnings and Cautions
General
• External debrillation equipment should be available for immediate use during the
implantation procedure and follow-up.
• Use the programmer only with the external power supply packaged with the programmer.
Using other accessories may cause damage to the programmer.