Stryker iSwitch Operation And Maintenance Manual
Stryker iSwitch Operation And Maintenance Manual

Stryker iSwitch Operation And Maintenance Manual

Wireless universal foot control
Hide thumbs Also See for iSwitch:

Advertisement

Endoscopy
iSwitch
Wireless Universal
Foot Control
Operation and Maintenance Manual
PATENTS PENDING

Advertisement

Table of Contents
loading

Summary of Contents for Stryker iSwitch

  • Page 1 Endoscopy iSwitch Wireless Universal Foot Control Operation and Maintenance Manual PATENTS PENDING...
  • Page 2: Table Of Contents

    Table of Contents Table of Contents ..................... 1 Warnings and Cautions .................. 2 Symbol Definitions ..................3 Product Description / Intended Use ............4 The Footswitch ..................... 5 The Receiver ....................6 Front Panel....................6 Rear Panel ....................7 Setting Up the Footswitch System ..............
  • Page 3: Warnings And Cautions

    Warnings and Cautions Please read this manual and follow its instructions carefully. The words warning, caution, and note carry special meanings and should be carefully reviewed: WARNING The personal safety of the patient or physician may be involved. Disregarding this information could result in injury to the patient or physician.
  • Page 4: Symbol Definitions

    WARNING by, or on order of, a physician. Stryker Endoscopy reserves the right to make improvements to the product described herein. The product therefore may not agree in detail to the published design or specifications. All specifications are subject to change without notice.
  • Page 5: Product Description / Intended Use

    The iSwitch is intended for use in surgical procedures where footswitch-operated devices, such as the Stryker TPS or SERFAS systems, are normally used. The iSwitch consolidates the functions of these devices into one wireless footswitch, freeing the operating room from excessive cables and foot controls.
  • Page 6: The Footswitch

    The Footswitch The footswitch rests on the operating-room floor and provides foot control of all devices connected to the iSwitch system. The footswitch houses three buttons and two pedals, which enable the user to alternate between operating-room devices and perform device-specific functions. When a button or pedal is pressed, the footswitch transmits a radio signal to the receiver, where the command is then routed to the appropriate device.
  • Page 7: The Receiver

    The Receiver The receiver connects to the devices that will be controlled by the iSwitch system. It receives commands sent from the footswitch and routes them to the appropriate device. The receiver also determines how footswitches are used and which devices they will control.
  • Page 8: Rear Panel

    Rear Panel Figure 5: The receiver rear panel TPS output: Provides a dedicated connection to the TPS console, enabling the commands issued from the footswitch to be routed to the TPS console. SERFAS output: Provides a dedicated connection to the SERFAS console, enabling the commands issued from the footswitch to be routed to the SERFAS console.
  • Page 9: Setting Up The Footswitch System

    Setting up the iSwitch Setting Up the Receiver Position the receiver on a Stryker cart or other sturdy platform. Connect the AC Power. • Connect the AC power cord to the AC input on the rear receiver panel. • Connect the other end to a hospital-grade receptacle.
  • Page 10: Setting Up The Footswitch

    Setting Up the Footswitch Insert the Stryker Battery Pack (P/N 277-300-100). It is recommended to use the Stryker Battery Pack to achieve Note maximum battery life and prevent improper insertion. • Twist off the cap on the side of the footswitch by turning 1/2 turn counterclockwise.
  • Page 11: System Settings

    System Settings Using the 2 mode buttons on the Receiver, the system Settings may be modified as listed below: To enter the Settings mode Press and hold both mode buttons on the Receiver for 5 seconds • In this mode, the left (Footswitch 1) mode button toggles among options.
  • Page 12: Operating The Footswitch System

    Note recommended to keep the footswitch clean during use. Contact your local Stryker representative for ordering information. The iSwitch system is operated through the controls on the footswitch and the controls on the receiver. Using the Footswitch Controls Press the mode button to select which device the footswitch will control.
  • Page 13: Serfas Mode

    Increase Cut Level Coag Using the Receiver Controls While the footswitch controls the devices connected to the iSwitch system, the receiver controls how the footswitch functions. Receiver controls are used for selecting which device the footswitch will control, unsynchronizing footswitches, and merging footswitches.
  • Page 14: Cleaning And Maintenance

    The batteries may explode or leak if recharged, inserted improperly, or disposed of by fire. Note Replace the battery pack with a Stryker Battery Pack (P/N 277- 300-100) for optimal battery performance. Battery Disposal The batteries must be disposed of according to local laws and hospital practices.
  • Page 15: Troubleshooting

    Troubleshooting Problem Possible Solution No results when the • Press buttons I or III to wake Footswitch. Footswitch is pressed. • Synchronize the Footswitch. • Replace batteries. The Footswitch will not • Hold the Footswitch synchronization icon synchronize with the within one inch of the receiver synchroni- receiver.
  • Page 16: Technical Specifications

    Technical Specifications Environmental Specifications Operating Temperature: 10° to 40°C Humidity: 35% to 75% RH Shipping/Storage Operating Temperature: 10° to 40°C Humidity: 35% to 75% RH System Input Power Requirements Voltage: 100-240 VAC Frequency: 50/60 Hz Current: 0.6 Amps Fuse Rating: 1.0A/250V Classifications Receiver: Class I Equipment...
  • Page 17 Wireless USB Specifications Frequency range: 2.402 Hz -- 2.478 GHz Modulation: Direct Sequence Spread Spectrum (DSSS) Power: 0 dBm RFID Specifications Frequency: 125 KHz Modulation: Binary Pulse Length Modulation (BPLM) Power: <0.001W FCC ID SSH-WUF IC ID 4919C-WUF Standards Compliance IEC 60601-1:1988 + A1:1991 + A2:1995 IEC 60601-1-2: 2001 IEC 60601-2-2:1998...
  • Page 18: Electromagnetic Compatibility

    Guidance and Manufacturer's Declaration: Electromagnetic Emissions iSwitch is intended for use in the electromagnetic environment specified below. The customer or the user of iSwitch should ensure that it is used in such an environment. Emissions test...
  • Page 19 Guidance and Manufacturer's Declaration: Electromagnetic Immunity iSwitch is intended for use in the electromagnetic environment specified below. The customer or the user of iSwitch should ensure that it is used in such an environment. Electromagnetic IEC 60601 Test Immunity Test...
  • Page 20 To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the iSwitch system is used exceeds the applicable RF compliance level above, the iSwitch system should be observed to verify normal opera- tion.
  • Page 21 Recommended Separation Distances Between Portable and Mobile RF Communications Equipment and the iSwitch System The iSwitch system is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The user of the iSwitch system can help prevent electromagnetic interference by maintaining a mini- mum distance between portable and mobile RF communications equipment (transmitters) and the iSwitch sys- tem as recommended below, according to the maximum output power of the communications equipment.
  • Page 22: Warranty Statement

    (i.e. neglect, dropping, or denting) or by failure to follow the procedures outlined in this manual or demonstrated by Stryker Endoscopy representatives. Unauthorized repair or modifications to the iSwitch may void the warranty and invalidate the user’s authority to use the product.
  • Page 23: Other Service

    Other Service For service in the U.S.A., call your Stryker Endoscopy representative or call Stryker Endoscopy Customer Service at 1-800-624-4422. Outside of the U.S.A., please contact your Stryker Endoscopy distributor at one of the following locations: Stryker Corporation Stryker European Rep - RA/QA Manager...
  • Page 25 Stryker Finland Stryker Middle East / Africa PL 80 (Makelankatuz) Via Della Posta FIN 00501 Helsinki 6934 Bioggio FINLAND Switzerland Phone:358 (0) 9 7744 680 Phone:(4021) 212-1122 Fax:358 (0) 9 7744 6820 Fax:(4021) 212-1133 Stryker Korea NV Stryker SA (Belgium) 11F Dong Sung Bldg.

Table of Contents