Astro Med PSGBASE PSG Base physiological signal recording User Manual AURA title

Astro-Med, Inc. PSG Base physiological signal recording AURA title

User Manual

Phone 401.828.4000 • Fax 401.822.2430 • Technical Support 877.472.7779 • E-mail grass-telefactor@astromed.comWeb site: www.grass-telefactor.comUSERS MANUALManual Part Number M636K05600 East Greenwich Avenue, West Warwick, RI 02893AURA® PSGGRASS-TELEFACTOR®WITH AURAPSG AMPLIFIER SYSTEMWIRELESS /AMBULATORY RECORDERRelease A
© COPYRIGHT 2005 ASTRO-MED, INC.This manual is copyrighted with all rights reserved. No part of this manualmay be reproduced, transmitted, transcribed, stored in a retrieval system, ortranslated into any language in any form by any means without writtenpermission of Grass-Telefactor, An Astro-Med, Inc. Product Group.Information in this document is subject to change without notice. Astro-Med,Inc. assumes no responsibility for any errors, omissions or inaccuracieswhatsoever. The software described in this document is furnished under asoftware license agreement. The software may be used only in accordancewith the terms of this agreement. Except as permitted by the software licenseagreement, no part of this software may be reproduced, transmitted,transcribed, stored in a retrieval system, or translated into any language, inany form or by any means, electronic, mechanical, magnetic, optical, chemical,or manual, including photocopying, anywhere in the world without thewritten permission of Astro-Med, Inc.TRADEMARKSAURA®, Aurora®, Beehive®, Beehive Millennium®, Brain Navigator®,BrainTree®, Comet®, EZM®, EC2®, FASS™, Gamma®, GrassLab®, Heritage®,H2O®, Panorama®, PolyVIEW®, SAFELEAD®, SleepTrek®, Sonoma®, SzAC®,TWin® and TWinLOOK® are trademarks of Astro-Med, Inc.CompactFlash® is a trademark of SanDisk Corporation.Windows® is a trademark of Microsoft Corporation.Bluetooth™ is a trademark of Bluetooth SIG, Inc.PureLight® is a trademark of Nonin Medical, Inc.Other brand and product names are trademarks or registered trademarks oftheir representative holders.Printed in the United States of America
AMPLIFIER SYSTEM IDENTIFICATION DATACongratulations. Your Grass-Telefactor purchase is an investment in the finest ofstate-of-the-art medical technology. The information provided below lists the modelnumber and serial number of your Amplifier system. If, for any reason, it should benecessary for you to contact Astro–Med, Inc. regarding your purchase, please refer tothe following:Amplifier Serial Number: ______________________Base Station Serial Number:______________________IMPORTANTThis manual is subject to periodic review, update, and revision. Customers arecautioned to verify that the manual’s information applies to the software andhardware present in the equipment.This product performs as described in this manual, and in accompanying labelsand/or inserts, when assembled, operated, maintained, and repaired in accordancewith the instructions provided.This product must be cleaned and checked periodically. Do not use a defectiveproduct. Parts that are broken, missing, worn, or contaminated should be replacedimmediately. If repair or replacement becomes necessary, call or write to requestservice advice from Grass-Telefactor.This product must not be altered without the prior written approval ofGrass-Telefactor. The user of this product shall have the sole responsibility for anymalfunction that results from improper use, faulty maintenance, improper repair,unauthorized service, or alteration by anyone other than Grass-Telefactor.The safety, reliability, and performance of this device can only be assured under thefollowing conditions:•If the device has been used according to the accompanyingoperating instructions.•If changes or repairs have been carried out by Grass-Telefactor.•If it is used in buildings having ground equalization wiring that complieswith relevant UL, CSA, IEC or other local standards and regulations.
REGULATORY NOTICESThis device has been designed and certified to comply with the requirementsof the international standard EN60601-1 and EN60601-2-26, EN60601-1-2, andEN60601-1-1 the United States standard UL 60601-1, and the Canadianstandard CAN/CSA22.2 No.601.1.The device is classified:CLASS I, Type BF100-250 VAC, 50/60 Hz, 80 VAThe above classification is based on the condition that this device is installedand configured according to the instructions supplied. In order for thecomplete system to maintain compliance with the relevant standards, the hostcomputer must be approved to the IEC950 standard.This equipment has been tested and found to comply with the limits for aClass B digital device, pursuant to part 15 of the FCC Rules. These limits aredesigned to provide reasonable protection against harmful interference in aresidential installation. This equipment generates, uses and can radiate radiofrequency energy and, if not installed and used in accordance with theinstructions, may cause harmful interference to radio communications.However, there is no guarantee that interference will not occur in a particularinstallation. If this equipment does cause harmful interference to radio ortelevision reception, which can be determined by turning the equipment offand on, the user is encouraged to try to correct the interference by one or moreof the following measures:•Reorient or relocate the receiving antenna.•Increase the separation between the equipment and receiver.•Connect the equipment into an outlet on a circuit different from thatto which the receiver is connected.•Consult the dealer or an experienced radio/TV technician for help.This device complies with part 15 of the FCC Rules. Operation is subject to thefollowing two conditions:1. This device may not cause harmful interference, and2. This device must accept any interference received, includinginterference that may cause undesired operation.
EQUIPMENT CLASSIFICATIONSShock Prevention: Class 1Degree of Protection Against Harmful Ingress of Water: Ordinary Equipment, IPX0Degree of Safety in the Presence of Flammable Anesthetic Mixture with Air or withOxygen or Nitrous Oxide: Equipment not suitable for use in the presence of aflammable anesthetic mixture with air, oxygen, or nitrous oxide.Mode of Operation: ContinuousWARNINGSELECTRIC SHOCK HAZARDWarning: Connect the Base Station Power Supply only to a three-wire,grounded, hospital-grade receptacle. The three-connector plugmust be inserted into a properly wired three-wire receptacle. If athree-wire receptacle is not available, a qualified electrician mustinstall one in accordance with the governing electrical code.Warning: Do not use extension cords or adaptors of any kind. The powercord and plug must be intact and undamaged.Warning: The appliance coupler (AC Cordset) is the means fordisconnecting the Base Station from the power mains.Warning: Measure the system’s leakage current after completion ofinstallation, after disconnect/reconnection of parts of the system,and at regular periodic intervals. For instructions on how toperform this test please contact Grass-Telefactor TechnicalSupport. Forward and reverse polarity: 500 microamperesmaximum.EXPLOSION HAZARDWarning: Do not use this system in the presence of flammable anestheticsor other flammable substances.Warning: Use only the specified battery (part number 26759200) in theAURA PSG Amplifier. Use of unauthorized battery may causeexplosion/fire hazard.
PATIENT SAFETYWarning: The patient should be disconnected from the AURA PSG systemwhen high frequency surgical equipment is used.Warning: This system should not be used in place of electrocardiograph forvital signs monitoring.Warning: Use only by or on the order of medically trained personnel.Warning: Battery Charger must not be located in a patient area.Warning: Do not use in an MRI environment.Warning: Read manual before using.Warning: Protect from exposure to liquids. If the Amplifier Unit is exposed toliquids during recording, discontinue use by disconnecting theelectrodes from the Amplifier Unit and turning the Amplifier Unitpower off. Resumption of recording is to be performed only byqualified personnel.Warning: AURA PSG contains no user serviceable parts.Warning: AURA PSG is not intended to be sterilized.Warning: Use only Nonin-manufactured PureLight® pulse oximeter sensors.These sensors are manufactured to meet the accuracy specificationsfor Nonin pulse oximeters. Using other manufacturers’ sensors canresult in improper pulse oximeter performance. A list of compatiblesensors is provided in CHAPTER 5: ACCESSORIES AND REPLACEMENT PARTS.Warning: Loss of pulse oximeter monitoring can result if any objects hinderthe pulse measurement. Ensure that no blood flow restrictors (e.g.,blood pressure cuff) hinder pulse measurements.Warning: As with all medical equipment, carefully route cables andconnections to reduce the possibility of entanglement orstrangulation.Warning: This pulse oximetry system is designed to determine the percentageof arterial oxygen saturation of functional hemoglobin. Significantlevels of dysfunctional hemoglobin, such as methemoglobin, mightaffect the accuracy of the measurement.Warning: Inspect the pulse oximeter sensor application site at least every6 to 8 hours to ensure correct sensor alignment and skin integrity.Patient sensitivity may vary due to medical status or skin condition.Discontinue use of adhesive tape strips if the patient exhibits anallergic reaction to the adhesive material.Warning: The accuracy of the SpO2 measurement may be affected if the totalpulse oximeter cable length (including extension cables) is greaterthan 3 meters.
INTENDED USEThe AURA PSG amplifier system is intended for recording routineelectroencephalography (EEG) and polysomnography (PSG).The device is intended to be used only by physicians, technicians, or othermedical professionals that are trained in electroencephalography orpolysomnography.CAUTIONFederal law restricts this device to sale by or on the order of a licensedphysician (or properly licensed practitioner).Use only the Nonin probes as the optional pulse oximeter.Use only accessories and electrodes identified for use with this device(see instructions for the electrodes that are being used).Disconnect power supply before servicing.Disconnect the AURA PSG before using a defibrillator.The use of pulse oximeter accessories, sensors, and cables other than thosespecified by Grass Telefactor may result in increased emission and/ordecreased immunity of this device.The AURA PSG wireless mode uses the 2.4 GHz ISM band. Performance maybe impacted by other devices using this frequency, including Wi-Fi terminals,Bluetooth PDAs and some cordless phones.
AURA® PSG Wireless/Ambulatory Recorder 1-11Specifications & Symbols GlossarySpecificationsAURA PSG SYSTEM SPECIFICATIONSAmplifier__________ Grass-Telefactor AURA PSG system13 referential electrode inputs2 reference electrode inputs7 differential inputs2 DC coupled inputs1 connection for a Nonin pulse-oximeterAMPLIFIER SPECIFICATIONSREFERENTIAL ELECTRODE INPUTSInput Signal Range _ 4 mV peak to peak full-scaleInput Impedance ___ 12 Megohm or higher, all inputs including referenceDifferential Input Impedance _____ 20 Megohm or higherAmplitude Accuracy_ ±2.5 % (prior to software correction)Frequency Response 0.5 Hz to 50 Hz (-3 dB points, within 10%)Enhanced Low Frequency with TWin ______ 0.1 Hz (-3 dB, within 10%)CMR (60 Hz) _______ >80 dB (signal referenced) or >100 dB (earth reference)Noise ____________ <2 µV peak to peakInput Bias Current __ <4 nACross-Talk ________ 0.1% or lessMaximum Input ____ 4 mV
1-2 Chapter 1 Specifications & Symbols GlossaryDIFFERENTIAL INPUTSInput Signal Range _ 4 mV peak to peak full-scaleInput Impedance ___ 12 Megohm or higherAmplitude Accuracy_ ± 2.5 %Frequency Response 0.5 Hz to 50 Hz (-3 dB points, within 10%)Enhanced Low Frequency with TWin ______ 0.1 Hz (-3 dB, within 10%)CMR (60 Hz) _______ >80 dB (signal referenced) or >100 dB (earth reference)Noise ____________ <2 µV peak to peakInput Bias Current __ <350 nACross-Talk ________ 0.1% or lessMaximum Input ____ 4 mVISOLATED DC INPUTSInput Signal Range _ ±2.0 VFrequency Response 50 Hz (-3 dB points, within 10%)Cross-Talk ________ 1% or lessImpedance Test Mode ______ Referential inputs only: 1 kohms to 100 kohms, 10%Calibration Signal __ Referential inputs only: 500 µV peak to peak ±2%Sampling Rate _____ 200 samples/second/channelPower ____________ Rechargeable 3.6 V lithium batteryCapacity: 10 hours in the wireless mode, 12 hours in thetethered modeCharging: The battery must only be charged with theexternal Grass-Telefactor 42050100 Battery Charger thatoperates from a DC voltage supplied by the externalRPS-21903 Power Supply (see the separate BatteryCharger operating instructions)Physical Size ______ Amplifier Unit approximately:3.5" W x 5.9" H x 1.0" D (8.9 cm x 14.9 cm x 2.5 cm)Weight: 10 ozs. (280 g)
AURA® PSG Wireless/Ambulatory Recorder 1-3BASE STATION SPECIFICATIONSNON-ISOLATED DC INPUTSInput Signal Range _ ±2.5 VFrequency Response 50 Hz (-3 dB points, within 10%)Cross-Talk ________ 1 % or lessDC Channels ______ 2 channels±2.5 VConnectivity to Host PC ______ Standard 10Base-T Ethernet, TCP/IP protocolPower ____________ Medical-grade Isolated Power SupplyPhysical Size ______ Base Station approximately:7" W x 7.5" H x 2.7" D (17.8 cm x 19.1 cm x 6.9 cm)Weight: 2.3 lbs. (1.04 kg)BUILT-IN OXIMETER: USE ONLY WITH NONIN PURELIGHT SENSORSOximeter Saturation Range _________ 0 to 100%Pulse Rate Range __ 18 to 300 pulses per minuteMeasurement Wavelengths ____ Red: 660 nm at 3mW nominalInfrared: 910 nm at 3mW nominalAccuracy _________ SpO2 (70-100%) (±1SD*):No Motion: Adults, Pediatrics ±2 digitsNeonates ±3 digitsMotion: Adults, Pediatrics ±2 digitsNeonates ±3 digitsLow Perfusion: Adults, Pediatrics ±2 digitsNeonates ±3 digitsHeart Rate:No Motion (18-300 bpm): Adults, Pediatrics, Neonates ±3 digitsMotion (40-240 bpm): Adults, Pediatrics, Neonates ±5 digitsLow Perfusion (40-240 bpm): Adults, Pediatrics, Neonates ±3 digits* Standard Derivation is a statistical measure: up to 32% of the readings may fall outside these limits.
1-4 Chapter 1 Specifications & Symbols GlossaryOTHER SPECIFICATIONSRegulatory ________ AURA PSG System: certified toUL 60601-1CAN/CSA C22.2 No. 601.1IEC 60601-1-1IEC 60601-2-26EN 60601-1-2CE marked to EC MDD (93/42/EEC)Warranty__________ Lifetime Limited Warranty on Grass-Telefactormanufactured parts (see our full warranty for details)Software __________ Fully supported by TWinRPSAS40 MEDICAL-GRADE POWER SUPPLYInput _____________ 100 to 260 VACLine Frequency: 47 to 63 HzAmbient Operating Temperature: 0 to 40°CIEC320 Power Inlet, Removable 8-foot (2.4 m)Hospital-grade CordsetOutput ___________ +12 VDC Regulated, 1.2 Amperes maximumShort Circuit ProtectedLine/Load Regulation: ±5% OverallOutput Cable: 6 foot (1.8 m)Agency Approvals__ Conforms to UL2601-1 and certified toCAN/CSA C22.2 No.601.1,Certified to IEC60601-1 and TUV601.1 approvedPhysical Size ________ 3" W x 1.89" H x 4.75" L (7.6 cm x 4.8 cm x 12 cm)Weight: 1 lb. (0.45 kg)SYSTEM TRANSPORT OR STORAGE SPECIFICATIONSAmbient Temperature Range __________ -40° C to +70° CRelative Humidity Range __________ 10% to 100%, including condensationAtmospheric Pressure Range __ 500 hPa to 1060 hPa(All specifications subject to change without notice.)
AURA® PSG Wireless/Ambulatory Recorder 1-5Direct CurrentCourant ContinuOn (only for a part of equipment)Marche (seulement pour une partie de l’appareil)Off (only for a part of equipment)Arret (seulement pour une partie de l’appareil)Attention, consult accompanying documentsAttention, consulter les documents d’accompagnementProtective EarthTerre de ProtectionIsolated InputsEntrées IsoléesNon-ionizing electromagnetic radiationRayonnement électromagnétique non ionisantGLOSSARY OF SYMBOLS
1-6 Chapter 1 Specifications & Symbols Glossary
AURA® PSG Wireless/Ambulatory Recorder 2-12IntroductionProduct DescriptionThe AURA PSG system is designed specifically for recording EEG and PSG.The system features a compact, wearable 24-channel Amplifier Unit and a BaseStation that can be mounted in a variety of locations.The AURA PSG system provides for patient safety isolation, signalconditioning (physiological signal amplification and filtering), and digitization.The host computer receives data according to a specific protocol.Grass-Telefactor TWin® software can be used on the host computer to receiveand process the data. The TWin software is powerful and easy to use,providing data acquisition, recording, and review capabilities in one flexiblepackage.By combining over 70 years of neurophysiological amplifier experience withthe latest digital design techniques, the AURA PSG continues with the quality,reliability, and simplicity that have made Grass-Telefactor famous in the field ofneurophysiology.FEATURES•Compact design that is rugged, lightweight and easy to use•Local analog to digital conversion for interference-free recordings•Easily connect to any PC with the on-board Ethernet connection•Built-in impedance checking and calibrations•Amplifier Unit is wearable for ambulatory applications•Wireless mode allows ambulatory applications within 25 feet (withoutobstructions) of the Base Station.
2-2 Chapter 2 IntroductionFigure 2-1: Amplifier UnitAMPLIFIER UNITThe unit is enclosed in a plastic housing approximately 3.5” W x 5.9” H x 1.0” D(8.9 cm x 14.9 cm x 2.5 cm) in size. It is small and light enough to be worncomfortably.The Amplifier Unit provides 22 isolated, analog waveform inputs along withtwo additional channels generated by a Nonin pulse oximeter. Electrode andsensor connection is direct to the unit with no adaptor required.Following is a list of the analog inputs with connector type:13 AC Referential SAFELEAD electrode connection1 AC Differential Pair of SAFELEAD electrode connections6 AC Differential 2-pin molded connectors2 DC 2-pin molded connectorsThere are also SAFELEAD electrode connections for two Ref inputs and one GND(common). The Amplifier Unit can operate in either standard or wireless modes.STANDARD MODEThe Amplifier Unit can be tethered to the Base Station, which streams data to ahost computer. When tethered, the Amplifier Unit connects to the Base Station viaa single cable that carries power and data through a proprietary serial interface.The Amplifier Unit is also capable of operating un-tethered. When un-tethered,it will run off a battery and save data on a CompactFlash® memory card.WIRELESS MODEThe Amplifier Unit uses Bluetooth® technology to stream data to a host computervia a wireless connection with the Base Station. The Amplifier Unit must be within25 feet (without obstructions) of the Base Station. The Amplifier Unit is poweredby a battery and does not use a CompactFlash card or Tether Cable.AURAPSGDC1RATSnoreAirflowSpO2PulseECG+CH13Chin3Chin1C3O1ROCA1REF
AURA® PSG Wireless/Ambulatory Recorder 2-3Figure 2-2: Base StationBASE STATIONThe Base Station is enclosed in a plastic housing approximately 7” W x 6” H x2” D (17.8 cm x 15.3 cm x 5.1 cm) in size and it can be attached to a cart arm,mounted on a wall next to a patient bed, or sit flat on a tabletop.The Base Station converts data from the Amplifier Unit to network protocolsfor transfer to a host computer. See CHAPTER 3 INSTALLATION, FIGURE 3-6.The LCD display with menu controls is located on the top surface of the BaseStation. Menu selections can be made for configuring the unit, communicatingwith the host computer, and implementing the electrode impedance test. TheLCD also displays status information such as electrode impedance test values.A Tether Cable connection port is also located on the top surface of the BaseStation. This is used to connect the Amplifier Unit to the Base Station via theTether Cable in standard mode. The Base Station also contains Bluetoothtechnology to receive data from the Amplifier Unit in wireless mode.AURA-PSG Base Station
2-4 Chapter 2 IntroductionPower is supplied to the Base Station through a rear sideconnector that attaches to the RPSAS40 Medical-gradePower Supply (+12 VDC). The RPSAS40 Power Supplymodule provides low-voltage (+12 VDC) to power theBase Station. Only certified Grass-Telefactor regulatedpower supplies can be used with the AURA PSG system.A 36-pin connector is also located on the rear side and itallows for the connection of an optional PatientEventbutton (CAB-21648-10). Two Auxiliary DC inputsare available for recording external voltage sources. Allother connections are also located on the rear side of theBase Station.BATTERY & BATTERY CHARGERA rechargeable 3.6 V lithium ion battery (267592000) provides power to theAmplifier Unit. The Battery Charger is a free-standing unit that can charge asingle battery. The Battery Charger is external and operates from a DC voltagesupplied by an external power supply.See the separate operating instructions for the Battery Charger.Warning: Battery Charger must not be located in a patient area.Figure 2-3: RPSAS40Power Supply
AURA® PSG Wireless/Ambulatory Recorder 2-5AUXILIARY DC INPUT MODULE (DCM8)The auxiliary DC Input Module, DCM8, is a small plastic enclosure witheight non-isolated 3.5 mm input jacks for DC inputs and one 3.5 mm input jackfor an event pushbutton. Four of the DC inputs are single ended and four aredifferential to allow for the greatest flexibility when connecting auxiliarydevice outputs.Figure 2-5: DCM8 DC Input ModuleThe DCM8 is supplied standard with the Model AUXL-P AURA PSG System,but is an opion with the Model AU-P AURA PSG Portable System.For more information regarding the compatibility of a device with the AURAPSG system, please contact Grass-Telefactor, Technical Support ServicesDepartment. The optional Nonin PureLight® Pulse Oximeter Sensors can beconnected directly to the Amplifier Unit.DCM8AUXILIARY DC INPUT MODULESINGLE ENDED DIFFERENTIALEVENT26153748
2-6 Chapter 2 IntroductionSYSTEM COMPONENTSSTANDARD SYSTEM COMPONENTSThe following components are included in the Model AUXL-P AURA PSGPC-based system:•AURA PSG Amplifier System withBuilt-in OximeterCompactFlash card and readerAmplifier Battery (2) with battery charger and power supplyPouch for AURA PSG Amplifier and 4 sizes of straps•Base Station withWall-mount bracketRPSAS40 Medical-grade Power SupplyTether cable (CAB-21916)•NET-CKIT Network cabling kit (Base Station to Host)•DCM8 DC Input Module with wall-mount bracket•20-button programmable keypad for notation entry and systemoperation•Medical-grade Isolated Power SystemThe following components are included in the Model AU-P AURA PSGPortable Laptop-based system:•AURA PSG Amplifier System withBuilt-in OximeterCompactFlash card and readerAmplifier Battery (2) with battery charger and power supplyPouch for AURA PSG Amplifier and 4 sizes of straps•Base Station withWall-mount bracketRPSAS40 Medical-grade Power SupplyTether cable (CAB-21916)•NET-CKIT Network cabling kit (Base Station to Host)OPTIONAL SYSTEM COMPONENTSRefer to CHAPTER 5: ACCESSORIES & REPLACEMENT PARTS, for a list of optionalsystem components.
AURA® PSG Wireless/Ambulatory Recorder 3-13InstallationSetting Up for OperationThe AURA PSG System is designed to be located in the vicinity of the testsubject, but with the ability to allow patient mobility for periods of time. TheAmplifier Unit can be placed inside a pouch worn by the patient.The Base Station itself, and the associated power supply, can be attached to acart or stand for routine EEG or PSG studies.Grass-Telefactor provides a full line of mobile carts and mounting brackets.Please consult Grass-Telefactor Customer Support for further details.Take care to locate these components away from dirt, dust, high-temperatures,and liquid spill hazards. Avoid locating the unit where the power switches orcontrols or cables could be bumped inadvertently.
3-2 Chapter 3 InstallationINSTALLATIONRefer to the interconnection diagram (Figure 3-6) for connection details andcable part numbers. To install the AURA PSG system, proceed with thefollowing steps.STEP 1: INSTALLING CABLINGSTEP 2: INSTALLING THE NETWORK INTERFACE CARD FOR ASSOCIATED COMPUTERSSTEP 3: SETTING UP THE RPSAS40 REGULATED POWER SUPPLYSTEP 4: SETTING UP THE BASE STATIONSTEP 5: CONNECTING THE TETHER CABLESTEP 6: CONNECTING AMPLIFIER UNIT INPUTSSTEP 7: CONNECTING OPTIONAL EQUIPMENT TO THE BASE STATIONSTEP 8: SETTING UP THE BATTERY CHARGERSTEP 9: SETTING UP WIRELESS COMMUNICATION (WIRELESS MODE ONLY)STEP 1: INSTALLING CABLINGGrass-Telefactor recommends that all cabling, network, video cabling, intercomcabling, and any other cabling for auxiliary instrumentation be run by qualifiedpersonnel under hospital supervision and according to local standards andregulations.It is good practice to use an approved isolation transformer wheninterconnecting multiple pieces of equipment to the AURA PSG system toavoid summation of leakage currents. The use of an isolation transformerreduces the leakage current to that of the isolation transformer. If an isolationtransformer is to be used it should be EN60601-1 approved and rated for115/240 VAC, 50/60 Hz, 600-800 VA.STEP 2: INSTALLING THE NETWORK INTERFACE CARDFOR ASSOCIATED COMPUTERSThe AURA PSG system may be supplied with an optional network interfacecard for computers associated with the AURA PSG system. Follow theinstructions that are supplied with this card to install and test the interface cardbefore connecting to the AURA PSG system.
AURA® PSG Wireless/Ambulatory Recorder 3-3STEP 3: SETTING UP THE RPSAS40 REGULATED POWER SUPPLYSelect an appropriate location that will allow for ventilation around the unitand the outlet to be within safe reach of the Base Station. The power cableshould be run so as it will be out of the way and not be a tripping hazard.POWER SUPPLY LINE VOLTAGEThe RPSAS40 will operate with line voltage within the range of 100 to 250volts, covering both 115 and 230 volts operation with no user intervention.The proper hospital-grade AC power cord is required.STEP 4: SETTING UP THE BASE STATIONThe Base Station can be located remotely from or locally to the hostcomputer. Depending on the setup, the network cable required will be either across-over or patch 10BaseT Ethernet cable rated category 5 or higher.If a direct connection is used, a single cross-over cable is required(CAB-20576-03). If going through a dedicated hub or switch, a patch cable isrequired (CAB-21064-025 or CAB-21064-010). A networking cable connector(CON-20486) is also provided. Select the appropriate cable and connect theBase Station to the host computer.
3-4 Chapter 3 InstallationSTEP 5: CONNECTING THE TETHER CABLEConnect one end of the tethercable to the Base Station byinserting the connectorinto place, as indicatedbelow. To disconnectthe tether cable(26802001), pull on theouter sleeve of theconnector to unlockit from the unit.AURA-PSG Base StationNote: Do not twist the connector or damage will result.Connect the other end of the tether cable to theAmplifier Unit.Figure 3-1: Base Station tether cable connection (standard mode)Figure 3-2: Amplifier Unit tether cable connection (standard mode)AURAPSGDC1RATSnoreAirflowSpO2PulseECG+CH13Chin3Chin1C3O1ROCA1REF
AURA® PSG Wireless/Ambulatory Recorder 3-5The following inputs are availablethrough the Amplifier Unit:•13 referential electrode inputs•2 reference electrode inputs•7 differential inputs•2 DC coupled inputs•1 connection for a NoninPureLight® pulse-oximeterA list of compatible sensors isprovided in CHAPTER 5: ACCESSORIESAND REPLACEMENT PARTS.STEP 6: CONNECTING AMPLIFIER UNIT INPUTSAttach the inputs to the Amplifier Unit.AURAPSGDC1RATSnoreAirflowSpO2PulseECG+CH13Chin3Chin1C3O1ROCA1REFREFA1ROCO1C3Chin1Chin3CH13ECG+REFGNDA2LOCO2C4Chin2CH12ECG-SpO2 PulseAirflow-Airflow+Snore-Snore+RAT-RAT+DC1GNDChest-Chest+Abd-Abd+LAT-LAT+DC2GNDFigure 3-4: Amplifier Unit inputsFigure 3-3:Amplifier Unitconnections
3-6 Chapter 3 InstallationSTEP 7: CONNECTING OPTIONAL EQUIPMENT TO THE BASE STATIONAttach any additional equipment. Refer to Figure 3-6 for required cable numbersand connection locations.Waveforms from AUX 1 and AUX 2 DC input ports are only recorded when theAmplifier Unit is tethered to the Base Station. Some connections are reservedand should not be used.STEP 8: SETTING UP THE BATTERY CHARGERSee the separate operating instructions for the Battery Charger.STEP 9: SETTING UP WIRELESS COMMUNICATION (WIRELESS MODE ONLY)If the Amplifier Unit is used in wireless mode, the wireless connection betweenit and the Base Station must be established. This process is not required for theAmplifier Unit in standard mode.1. Connect the tether cable between the Base Station and Amplifier Unit, asindicated in STEP 5 CONNECTING THE TETHER CABLE.2. Turn on the Base Station power.3. Turn on the Amplifier Unit power.4. Select Set Wireless Pairing on the Base Station menu. Then press theENTER key.5. The Base Station will display Setting up Wireless.6. The Base Station will exchange wireless device addresses with theAmplifier Unit automatically, and then confirm the wireless connection.7. The Base Station will display Wireless Confirmed.8. Any time the Base Station and Amplifier Unit are both on and no tethercable is connected, the paired units will attempt to connect with eachother. They will connect only with each other, and attempts by a thirdTo OptionalEvent Buttonor DCM8Reserved Ethernet Cableto Computer To RPSAS40Power SupplyFigure 3-5: Base StationConnectionsneed info onthe antenna
AURA® PSG Wireless/Ambulatory Recorder 3-7Figure 3-6: AURA PSG connectionsAURA PSG Setupneed info onthe antennaBase StationCAB-21064Ethernet PatchCableTo PCEthernetCardCAB-20576-03Ethernet Cross-overCableCON-20486 NetworkingCable ConnectororTo Ethernet Hub or SwitchTo GroundedWall OutletRPSAS40 RegulatedPower Supply AC PowerLine InCAB-21617Optional Event PushbuttonCAB-21648-10Amplifier UnitWireless Mode Requires No Tether CableTether Cable26802001DCM8AUXILIARY DC INPUT MODULESINGLE ENDED DIFFERENTIALEVENT26153748orDCM8Optional Event ButtonCAB-21648-10AURAPSGDC1RATSnoreAirflowSpO2PulseECG+CH13Chin3Chin1C3O1ROCA1REF
3-8 Chapter 3 Installationdevice to connect will be rejected.SIGNAL DEFINITIONSThe Amplifier Unit includes labels for each input as a convenience to the user. Theconnector marked SpO2 Pulse is intended for a Pulse Oximeter sensor. Only thosesensors listed in the Accessories section of this manual should be used.Other connector labels match the default montage used by TWin software forthe AURA PSG. Following are signal definitions associated with these.Referential Inputs (AC coupled) with SAFELEAD® connectionsO1 & O2 Occipital electrodes as defined by the 10/20 standardC3 & C4 Central electrodes as defined by the 10/20 standardA1 & A2 Auricular electrodes as defined by the 10/20 standardLOC & ROC Left and Right Outer Canthus electrodesChin There are three electrodes provided for the chinCH12 & CH13 Optional electrodesThe Referential Inputs are designed for surface electrodes such as thosemanufactured by Grass and suggested in ACNS 1994 Guideline 1 (2.1). The REFconnects to the electrode used as the reference for Referential Inputs. The twoinputs with this label are connected together inside the device so that redundantelectrodes can be used.Differential Inputs (AC coupled)ECG ECG electrode pair (SAFELEAD)Chest & Abd Respiratory effort sensors (such as belts)Airflow Airflow sensor (such as thermocouples and thermistors)Snore Snore sensor (such as a microphone)LAT & RAT Left and Right Anterior Tibialis muscle electrodesThe Differential Inputs are intended for electrodes and sensors specificallydesigned for use with electrode compatible inputs. Appropriate electrodes andcompatible sleep sensors are available from Grass-Telefactor as well as othervendors. Additional guidance can be found in ACNS 1994 Guideline 15.Auxiliary Inputs (DC coupled)DC1 & DC2 Optional signal inputsWarning: All these inputs are connected to the patient side of the isolationbarrier. Never connect any of these inputs to a monitor or otherdevice unless it is fully isolated for patient safety.Warning: ECG and pulse oximetry measurements are not intended for usein vital signs monitoring. In any critical care environments, anindependent monitor must be provided.
AURA® PSG Wireless/Ambulatory Recorder 3-9HOST COMPUTER SETUPPower up the Base Station and enter a valid IP address for the unit. Computersassociated with the AURA PSG system should have the recording applicationsoftware installed and configured to work with this IP address to control theBase Station. See below for more information.If Grass-Telefactor TWin software is used on the host computer, refer to theTWin software manual for details on the operation of the system. A systemcalibration and test recording should be preformed following the instructionssupplied in the TWin manual.AURA PSG IP ADDRESS SETUPThis section will provide instructions on programming the IP address of theAURA PSG system. If applicable, it is possible choose an IP address that isconsistent with the existing networking scheme of the hospital.1. Make sure the Base Station is powered on.2. On the Base Station, push the MENU key four times to display the Set IPAddress option, and then press the ENTER key.3. Use the left and right keys to toggle to the next numeric entry.4. Use the up and down keys to change the numeric value.An example IP address is: 172.016.008.2005. When the IP address is finished, push the ENTER key to accept the entry.Note: If the MENU key is pressed while changing the IP address, themodifications will not be saved.SUBNET MASK SETUPThis section will provide instructions on programming the Subnet Mask of theAURA PSG system.1. Make sure the Base Station is powered on.2. On the Base Station, push the MENU button five times to display theSet Subnet Mask option, and then press the ENTER button.3. Use the up and down buttons to change the numeric value.An example Subnet Mask is: 255.255.255.0004. When the Subnet Mask is finished, push the ENTER button to acceptthe entry.
3-10 Chapter 3 InstallationAURA VERSIONTo check the version of the AURA amplifier before connection to applicationsoftware on the host computer:1. Make sure the Base Station is powered on.2. On the Base Station, push the MENU button six times to display theAURA Version option, and then press the ENTER button.3. The version of firmware and software will be displayed.NETWORK INTERFACE CARD (NIC) IP ADDRESS SETUPThis section will provide instructions on configuring computers associated withthe AURA PSG system. The IP address used for this section is different than theone entered in the previous section. If applicable, it is possible to choose an IPaddress consistent with the existing networking scheme of the hospital.1. From the Windows task bar, select Start > Settings > Control Panel.2. Double-click on the Network and Dial up Connections icon.3. In the Network and Dial up Connections window, double-click on the iconthat represents your NIC. This may be listed as Local Area Connection.4. In the Status window, click on the Properties button.5. Highlight Internet TCP/IP protocol by clicking on it once, then clickProperties. The Internet Protocol (TCP/IP) Properties window will appear.
AURA® PSG Wireless/Ambulatory Recorder 3-11Figure 3-8: Internet Protocol (TCP/IP) Properties window6. Select Use the following IP address.7. Enter an IP address that fits within the same series as the AURA PSG.Remember, the IP address here cannot be the same as the one used in theAURA PSG IP Address. An example IP address is: 172.16.8.199, or172.16.8.201.8. It may be necessary to change the Subnet Mask to 255.255.0.0.9. Click OK when finished.10. Close all windows and reboot the computer.
3-12 Chapter 3 Installation
AURA® PSG Wireless/Ambulatory Recorder 4-14OperationThe AURA PSG requires a host computer with appropriate software to be attachedvia a network cable to setup the system parameters. This section is an overview ofthe controls, indicators, and other features available for use on the unit.BASE STATIONThe controls available on the Base Station include the DC power switch on the rearand eight keys associated with the LCD. There are eight pushbuttons, or keys, forinteracting with the Base Station and the host computer. Some of the selections inthe menu require the host computer to be connected to the Base Station.Figure 4-1: Base Station Front Panel ControlsAURA-PSG Base Station
4-2 Chapter 4 OperationMENU SYSTEMThe MENU key is used to toggle through the main menu items or to back out ofa menu selection or submenu. ENTER selects the item to execute or proceed toa submenu item. The following list describes each key on the Base Station and abrief description of its use.MENU key toggles through the menu items or backs out of amenu selection back to the previous level. While in asubmenu or selection the MENU key can be used to canceland return back to the main menu.Provides no function for AURA PSG.The left/right arrows are used to navigate through asubmenu list.The up/down arrows are used to scroll through statusinformation such as electrode impedance results.The ENTER key selects the item to execute or proceedsto a submenu.E-TEST provides a shortcut to turn the electrode testfunction on without going through the menu selectionprocess.The following menu options are available:Status Reports communication errors with the data transfer.Oximeter Display* Displays the current readings of the Nonin PureLight® PulseOximeter on the LCD.Set IP Address** Allows an IP address for the device to be entered. Used toset the IP address of the Base Station. The left/right keysactivate the number in IP address to be changed and theup/down keys increment/decrement the active number.ENTER accepts the IP address.
AURA® PSG Wireless/Ambulatory Recorder 4-3CheckImpedances* Requests the host computer monitoring software toperform an electrode test and return the results for display.Z limit impedance selections include: 0.1, 0.5, 1, 2, 5, 10, 20,100 kohm.Press ENTER to select and use the left/right keys in the Zlimit selection menu. ENTER to execute the request. Use theup/down keys to scroll through the results returned fromthe application software on the host computer. MENUreturns to the main menu item list.E-TEST key executes a request to the application softwareon the host computer to perform an impedance test usingthe last Z limit selected. Press ENTER to begin calibration.Warning: The electrode impedance test should not be used withintra-cranial electrodes.Calibrate* Requests the host computer monitoring software to performa calibration for each channel.* Only available when connected to application software on host computer.** Only available when not connected to application software on host computer.INDICATORSA power indicator is located above the LCD and is green when the Base Stationpower is on. The LCD displays the menus, electrode impedance results,connection status, and any error messages that may occur.Additionally, two indicator lights are used by the Ethernet connection on theback of the Base Station. The green light indicates the Base Station is attachedto an active node, and the yellow light indicates communication activity overthe connection.
4-4 Chapter 4 OperationAMPLIFIER UNITThe controls on the Amplifier Unit are used toturn the power on and off.POWER BUTTONSTurns the Amplifier Unit power off.The button must be held for up totwenty seconds to turn the poweroff. This feature helps ensure thepower is not turned off accidentally.In error conditions, it may be necessary tohold the Power Off button in for aminimum of 30 seconds to turn off theAmplifier Unit power.Turns the Amplifier Unit power on.Figure 4-2: Amplifier Unit ControlsAURAPSGDC1RATSnoreAirflowSpO2PulseECG+CH13Chin3Chin1C3O1ROCA1REF
AURA® PSG Wireless/Ambulatory Recorder 4-5INDICATORSThere are three indicator lights on the Amplifier Unit. One green indicator lightprovides information about the power status of the Amplifier Unit. Two amberindicator lights are provided. One amber light provides information about theconnection between the Amplifier Unit and Base Station. The other amber lightprovides information about the Nonin pulse oximeter.GREEN POWER INDICATORSteady Amplifier Unit is powered by the tether cable(standard mode).Flashing Amplifier Unit is powered by battery.Off Amplifier Unit is not functioning.AMBER LINK INDICATORSteady The Amplifier Unit is connected to the Base Stationvia the tether cable (standard mode).Flashing Once every two seconds: The Amplifier Unit isrecording to a CompactFlash Card (standard mode).Flashing Once per second: The Amplifier Unit is within rangeof the Base Station (wireless mode).Flashing Faster than once per second: The Amplifier Unit isfinishing writing data to the CompactFlash Card(standard mode). This happens when theCompactFlash has filled or if the user is attempting toturn off the amplifier while it is writing data to theCompactFlash. In the latter case the user can releasethe power off button, the amplifier will turn off whenit is finished, usually within 30 seconds.AMBER PULSE OXIMETER INDICATORFlashing The pulse oximeter is reading a pulse between20 and 200.
4-6 Chapter 4 OperationCOMPACTFLASH CARD & BATTERYThe Amplifier Unit in standard mode, when untethered, is powered by an internalbattery and saves data on a CompactFlash memory card. CompactFlash is anindustry standard removable storage media. The battery is capable of running theAmplifier Unit in standard mode for approximately 12 hours.The Amplifier Unit in wireless mode is powered by the same internal battery,but does not use a CompactFlash card. The battery is capable of running theAmplifier Unit in wireless mode for approximately 10 hours.To open the CompactFlash/Batterycompartment, press the tabon the battery cover andslide the cover outward.Set the cover aside.Figure 4-3: CompactFlash Card & BatteryThe CompactFlash card drive is located behind the battery compartment. Forstandard mode operation, slide the CompactFlash card into the drive. The topof the card must face the bottom of the Amplifier Unit to be oriented properlyfor insertion (see Figure 4-3). To remove the card, simply pull it out of thedrive. For wireless mode operation, do not insert a CompactFlash card.Two batteries are shipped with each Amplifier Unit and will need to becharged prior to each use. Insert a fully-charged battery into the batterycompartment. Be sure to orient the battery correctly (see Figure 4-3).Warning: Use only the specified battery (26759200) in the AURA PSG.Use of unauthorized battery may cause explosion/fire hazard.To reattach the cover, slide the cover back into position. The tab will lock thecover in place.
AURA® PSG Wireless/Ambulatory Recorder 4-7BATTERY CHARGERThe battery must be charged prior to each use. See the separate operatinginstructions for the Battery Charger.Warning: Battery Charger must not be located in a patient area.CALIBRATIONThe AURA PSG system includes a built-in calibration signal generator and themeans to connect this generator to the referential amplifier inputs at the first stagepreamplifier. The generator outputs a 5 Hz, 500 µV peak-to-peak square wave. Thefrequency of this source can be set by the host computer but is generally 5 Hz.Gain calibration and correction is critical to the accurate creation of montages fromthe referentially recorded data. It is recommended that a calibration procedure beperformed prior to every recording as standard practice.Calibration controls are only available in the application software. However arequest can be sent from the Base Station via a menu item to have the applicationsoftware automatically perform a calibration. Refer to the instructions forcalibrating the amplifier hardware in the TWin software manual for more details.Typically calibration involves starting the recorder software, putting the AURAPSG into calibration mode, recording a segment of the calibration signal thenconfirming the peak-to-peak value of the AC calibration signal. This data is thenused to automatically generate a list of correction values for both offset and gain.ELECTRODE IMPEDANCE TESTThe AURA PSG system includes a built-in electrode test circuit that tests theimpedance of each electrode, including the reference, for referential inputs. Thisfunction can be executed from either the application software or at the Base Stationitself. The E-TEST key on the Base Station calls this function and the results aredisplayed on the LCD, based on the preferences set in the application software. Ifthe application software is not present this function cannot be selected.Warning: The electrode impedance test should not be used withintra-cranial electrodes.
4-8 Chapter 4 OperationRECORDING OVERVIEWTETHERED RECORDINGDuring tethered recording, the Amplifier Unit is used in standard mode. Itoperates while connected to the Base Station via a tether cable. Signals arestreamed to the host via this connection.During tethered recording, use caution to avoid contact with the AmplifierUnit “Off” button. The “Off” button must be held for 10 to 20 seconds to turnthe power off. This feature helps ensure the power is not turned offaccidentally.Ensure the following components are available for tethered recording:•Amplifier Unit with Tether Cable —The Amplifier Unit with TetherCable will be used to send signals to the Base Station.•Base Station —The Base Station is used to configure the Amplifier Unit.•Host Computer with TWin Software —The computer and TWinsoftware is used to initiate remote recording and review recordings.•Electrodes & Sensors —These measurement components will be usedto connect the patient input signals to the Amplifier Unit.STARTING TETHERED RECORDINGThe process for starting tethered recording requires the following steps:1. Connect the Amplifier Unit to the Base Station via the Tether Cable.2. Connect the patient electrodes to the Amplifier unit.3. Configure the Amplifier Unit using the Base Station and associated TWinhost software.4. Initiate recording using the TWin Recording feature. Waveforms willdisplay in the TWin software waveform area.Warning: Protect the Amplifier Unit from exposure to liquids. If theAmplifier Unit is exposed to liquids during recording,discontinue use by disconnecting the electrodes from theAmplifier unit and turning off the Amplifier Unit power.Resumption of recording is to be performed only by qualifiedpersonnel.STOPPING TETHERED RECORDINGRecording is stopped using the TWin software.
AURA® PSG Wireless/Ambulatory Recorder 4-9AMBULATORY RECORDINGDuring ambulatory recording, the Amplifier Unit is used in standard mode.When untethered, the Amplifier Unit will run off a battery and save data on aCompactFlash® memory card. The battery is capable of running the AmplifierUnit for approximately 12 hours.During untethered recording, use caution to avoid contact with the AmplifierUnit Off button. The Off button must be held for 10 to 20 seconds to turn thepower off. This feature helps ensure the power is not turned off accidentally.Ensure the following components are available for tethered recording:•Amplifier Unit with Tether Cable —The Amplifier Unit with TetherCable will be used to set up and initiate the recording.•CompactFlash Card & Battery —A CompactFlash card and fully-charged battery should be installed in the Amplifier Unit prior torecording.•Base Station —The Base Station is used to configure the Amplifier Unit.•Host Computer with TWin Software —The computer and TWinsoftware is used to initiate remote recording and review recordings.•Electrodes & Sensors —These measurement components will be usedto connect the patient input signals to the Amplifier Unit.STARTING AMBULATORY RECORDINGThe process for starting ambulatory recording requires the following steps:1. Connect the Amplifier Unit to the Base Station via the Tether Cable.2. Connect the patient electrodes to the Amplifier Unit.3. Configure the Amplifier Unit using the Base Station and associated TWinhost software.4. Initiate recording using the TWin Recording feature.5. Turn the Amplifier Unit power off and disconnect it from the Base Station.6. To start ambulatory recording, turn the Amplifier Unit power onWarning: Protect the Amplifier Unit from exposure to liquids. If theAmplifier Unit is exposed to liquids during recording, thepatient should discontinue use by disconnecting the electrodesfrom the Amplifier Unit and turning off the Amplifier Unitpower. Resumption of recording is to be performed only byqualified personnel.
4-10 Chapter 4 OperationSTOPPING AMBULATORY RECORDINGTo stop ambulatory recording, press and hold the Off button on theAmplifier Unit until the Amplifier Unit is turned off. This process may requireup to 30 seconds. The Amplifier Unit will turn off and recording will stop.READING AMBULATORY DATAThe process for reading ambulatory data requires a computer with aCompactFlash Card reader and software that can open the data files on thecard. The Base Station cannot be used to upload the data to the computer.When the extended ambulatory recording process is complete, the resultingdata files will be stored on the CompactFlash Card in the Amplifier Unit. Thedata is stored using a specific protocol.Grass-Telefactor TWin software can be used on the host computer to read thefile and process the data. The TWin software is powerful and easy to use,providing data acquisition, recording, and review capabilities in one flexiblepackage.Remove the CompactFlash Card from the Amplifier Unit. Then insert it into theCompactFlash Card reader on the computer. Although TWin software can readdirectly from the CompactFlash Card, it is recommended that data files becopied to a different medium such as the computer’s hard disk for furtherreview and analysis.
AURA® PSG Wireless/Ambulatory Recorder 4-11WIRELESS RECORDINGThe Amplifier Unit in wireless mode uses Bluetooth® technology to streamdata to a host computer via a wireless connection with the Base Station.The Amplifier Unit must be within 25-feet (7.5 m), without obstructions, ofthe Base Station.The Amplifier Unit in wireless mode is powered by a battery and must nothave a CompactFlash Card or Tether Cable attached.Ensure the following components are available for recording:•Amplifier Unit — The Amplifier Unit will be used to send signals tothe Base Station.• Battery — A fully-charged battery should be installed in the wirelessAmplifier Unit prior to recording.•Base Station — The Base Station is used to configure the Amplifier Unit.•Host Computer with TWin Software — The computer and TWinsoftware is used to initiate remote recording and review recordings.•Electrodes & Sensors — These measurement components will be usedto connect the patient input signals to the Amplifier Unit.STARTING RECORDINGThe process for starting recording requires the following steps:1. Ensure the Amplifier Unit is within 25-feet (7.5 m) of the Base Station.2. Connect the patient electrodes to the Amplifier Unit.3. Configure the Amplifier Unit using the Base Station and associated TWinhost software.4. Initiate recording using the TWin Recording feature. Waveforms willdisplay in the TWin software waveform area.Warning: Protect the Amplifier Unit from exposure to liquids. If theAmplifier Unit is exposed to liquids during recording,discontinue use by disconnecting the electrodes from theAmplifier Unit and turning off the Amplifier Unit power.Resumption of recording is to be performed only by qualifiedpersonnel.STOPPING RECORDINGRecording is stopped using the TWin software.
4-12 Chapter 4 Operation
AURA® PSG Wireless/Ambulatory Recorder 5-15Accessories & Replacement PartsAccessories & Replacement PartsPart Number Description14193512 512 MByte CompactFlash Memory Card26759200 Rechargeable 3.6 V lithium ion battery42050100 Battery ChargerRPS-21903 Battery Charger Power SupplyRPSAS40 AURA PSG Regulated Power SupplyIPS115 Isolated power system, 115-volt operation onlyIPS230 Isolated power system, 230-volt operation onlyCAB-21648-10 Optional Event pushbutton, 10’ (3 m) cable length, otherlengths availableDCM8 DC Input Module for up to 8 DC channelsKBD-21203-20 20-button Keypad for notation entry and system operationKBD-21203-58 Optional 58-button Keypad for notation entry and systemoperation32760200 AURA PSG Amplifier Pouch32760404 AURA Pouch Strap, Adult Large32760403 AURA Pouch Strap, Adult Small32760402 AURA Pouch Strap, Pediatric Large32760401 AURA Pouch Strap, Pediatric SmallACS-21651 Dedicated Ethernet Card for Base Station connectionfor use with a PCACS-20944-01 Dedicated Ethernet/Modem Card for Base Stationconnection for lap-top use
5-2 Chapter 5 Accessories & Replacement PartsOXIMETER SENSORSPart Number Description8000J Adult Flex Sensor, straight, 3-foot (1 m) length cable,includes a package of 25 8000JFW FlexiWrap® SensorWraps8000JFW FlexiWrap® Sensor Wraps, package of 258008J Infant Flex Sensor, straight, 40" (1 m) length cable,includes a package of 25 8008JFW FlexiWrap® SensorWraps8008JFW Infant FlexiWrap® Sensor Wraps, package of 257000A Adult Finger Flexi-form Disposable Sensors, 40" (1 m)length cable, package of 107000P Pediatric Finger Flexi-form Disposable Sensors, 40" (1 m)length cable, package of 108000AA Adult Articulated Finger Clip Sensor, 40" (1 m)length cable8000AP Pediatric Finger Clip Sensor, 40" (1 m) length cable8500I Patient Extension Cable, 40" (1 m) length cableCABLES/ADAPTORSPart Number Description26802001 Tether cable, 30-foot (10 m) length (Amplifier to Base Station)CAB-21916 Interface cable, 1/8” phone plug to PLU-880,5-foot (1.5 m) length (CPAP to DCM8)CAB-21615-5 DCM8 to Base Station patch cable, 5-foot (1.5 m) cableCAB-21616-10 Phono to 3.5 mm 10-foot (3 m) cable. Used to connectthe CAB-21648 event button to the DCM8 (included withCAB-21648)CAB-21617 Event button to Base Station adaptor, used to connect anevent button directly to the base when an optionalDCM8 DC Input Module is not available,1-foot (0.3 m) cable lengthMCB-21678-03 AC Cordset IEC320, 3-foot (0.9 m) cableMCB-20018 Hospital-grade AC cordset, USA, 6-foot (1.8 m) cableCAB-21911 Adaptor: (2) 1.5 mm SAFELEAD to Key ConnectorNET-CKIT Network Cabling Kit includes:CAB-21064-010 Ethernet cable, patch. Used to connect Base Station to Hostvia a hub/switch, 10-foot (3 m) cableCAB-21064-025 Ethernet cable, patch. Used to connect Base Station to Hostvia a hub/switch, 50-foot (15 m) cableCAB-20576-03 Ethernet cable, cross-over. Used to directly connect BaseStation to Host, 3-foot (0.9 m) cableCON-20486 Ethernet cable connector. Used to daisy chain two Ethernetcables (RJ45 connectors) together.
AURA® PSG Wireless/Ambulatory Recorder 5-3CARTS & MOUNTING BRACKETSPart Number DescriptionIT8/L Mobile Cart for use with a lap-top computerIT9 Mobile Rack Cart with drawer for full size keyboard,for use with a desktop PCARM-AS40 Adjustable Arm for mounting the Base Station on a MobileCartAS40WMB Base Station wall-mount bracketAS40WMB-QR Optional Base Station wall-mount bracket with quick releaseGRS-8399 DCM8 wall-mount bracketARM-AS40-QR Optional Adjustable Quick Release Arm for mounting theAURA on a CartTWIN PSG REVIEW WORKSTATIONPart Number DescriptionTRW-PSG Latest high-performance PC*, network ready and modem,CD-R/RW internal, Grass-Telefactor TWin PSG Review/Analysis software, Archive Manager, TWinLOOK, MicrosoftOffice, pcAnywhere softwareFPM-18 18" flat-panel/LCD monitorFPM-20 20" flat-panel/LCD monitorACS-21789 Flat-panel/LCD monitor wall-mount bracket
5-4 Chapter 5 Accessories & Replacement Parts
AURA® PSG Wireless/Ambulatory Recorder 6-16MaintenanceMaintenanceThere is no routine maintenance required for the Grass-Telefactor AURA PSGsystems other than normal periodic checks for unusual wear, cable abrasion,and routine cleaning.CALIBRATIONThe AURA PSG includes a built-in calibration signal source for verifyingproper operation and to simplify cross-channel gain correction and offsetadjustment. The calibration mode should be used to periodically generate a listof correction factors for use during the display and processing of the signaldata. Refer to the appropriate recording software instructions for details.
6-2 Chapter 6 MaintenanceCLEANINGPerform cleaning as needed.Warning:Electric Shock Hazard. Before cleaning the AC power supply orany AC line powered equipment, always turn off the power anddisconnect the power cord from the AC power supply.Cautions•Do not autoclave or pressure sterilize the AURA PSG system.•Do not soak or immerse the AURA PSG system in any liquid.•Do not gas sterilize the AURA PSG system.•Do not use petroleum based or acetone solutions, or other harshsolvents to clean the AURA PSG system.To clean the AURA PSG system, use a soft cloth dampened with mild soap andwater solution. To disinfect the Amplifier unit use 70% isopropyl alcohol. Besure that the components are unplugged before cleaning and that thecomponents are completely dry before use.ELECTRODESRefer to the cleaning instructions supplied with the electrodes for details oncleaning, disinfection, and/or sterilization.STORAGE & TRANSPORTATIONFor storage and transportation, it is recommended that the system and itsaccessories be within the temperature range of -40 to 70° C, 500 to 1060 hPa,and 10 to 100% RH, including condensation. When returning from temperatureextremes, allow the system to stabilize to room temperature before use.END-OF-LIFE DISPOSALWhen disposing of the AURA PSG system components at the end of life, it isrecommended that federal, state and local laws be followed for proper disposalof printed circuit boards, lithium-ion batteries, and plastic parts.Never incinerate or dispose of lithium-ion battery cells into fire.For disposal of non-Grass-Telefactor accessories, please follow the instructionsincluded with these items.
AURA® PSG Wireless/Ambulatory Recorder 7-17Troubleshooting GuidemotpmySesuaCelbaborPnoituloSthgilrewopnoitatSesaB noton noitatSesaBrewoPffohctiws nonruTnoitatSesaBnoitatSesaBrewop nideggulptonelbac yllufsigulprewopCDehttahtkcehC signirgnikcolehtdnadetresniylluf thgitdnahtondrocCA04SASPR yllufnideggulp drocCA04SASPRehtkcehCslangistneitapoN tneserp tontinureifilpmA esaBotgnitcennoc ylreporpnoitatSylreporpdetaessitinureifilpmAkcehCreifilpmAerusne,edomsseleriwroF ehtfo)m5.7(teef-52nihtiwsitinu noitatSesaBnoitatSesaB evisnopsernu tonelbactenrehtE nideggulp nosnoitcennocelbactenrehtEkcehC sdnehtobtcerrocnisserddaPItinuehttasserddaPIGSPARUAyfireV tcerrocsierawtfosgnidrocerehtnidnaretemixoroeslupoN ehtmorfsgnidaer thgiLeruP®tcerrocnirosgnidaerdeggulptonretemixO rotinureifilpmAotni nideggulptonrosnesehtfosnoitcennocelbackcehC thgiLeruP®noitatSesaBehthtobtarosnesdnanotnemecalprosneS tcerrocnitneitap ehtnitneitapnodecalpsirosnesyfireV lasopsidehtdnanoitatneiroreporp regnifehtottiserucesevisehdano2&1stupniXUA toneranoitatSesaB gnidrocernitneserp erawtfosdeggulptoneraselbaC yllufni snoitcennocgnilbacyfireV
7-2 Chapter 7 Troubleshooting GuidemotpmySesuaCelbaborPnoituloSnoitatSesaBnosyeK lanoitcnufton notonrewoPnoitatSesaBotrewopnonruTerawtfosgnidroceR tuodekcol sutatserawtfosgnidrocerkcehCnoyekTSET-EesaBnoitatSlanoitcnuftontonerawtfosgnidroceR gninnur erawtfosgnidrocertratSstluserTSET-EdaBedortcelerooP noitacilppa ylppaerdnanoitacilppaedortcelekcehC dedeenfitontinureifilpmA yllufnideggulp ylreporpderehtetsitinureifilpmAkcehCytilauqlangisrooPedortcelerooP noitacilppa ylppaerdnanoitacilppaedortcelekcehC dedeenfitontinureifilpmA yllufnideggulp ylreporpderehtetsitinureifilpmAkcehCecnerefretnIfosecruosevomerdnaetacoL ecnerefretni
AURA® PSG Wireless/Ambulatory Recorder A-1AAppendix AConnector Pin-outsETHERNET CABLE, CROSS-OVERUsed to connect Base Station directly to the Host computer.Connector type: RJ45Pin 1 = Pin 3Pin 2 = Pin 6Pin 3 = Pin 1Pin 4 = Pin 4Pin 5 = Pin 5Pin 6 = Pin 2Pin 7 = Pin 7Pin 8 = Pin 8ETHERNET CABLE, PATCHUsed to connect Base Station and Host computer through a dedicatednetworking hub/switch.Connector type: RJ45Pin 1 = Pin 1Pin 2 = Pin 2Pin 3 = Pin 3Pin 4 = Pin 4Pin 5 = Pin 5Pin 6 = Pin 6Pin 7 = Pin 7Pin 8 = Pin 8
A-2 Chapter A Connector Pin-outs
AURA® PSG Wireless/Ambulatory Recorder B-1BAppendix BService Policy & WarrantyWarranty repair and service for this system must be performed by aGrass-Telefactor service representative or at the Grass-Telefactor factory.To contact Grass-Telefactor, refer to the SERVICE AND WARRANTY on thefollowing pages.Do not use malfunctioning equipment. Make all necessary repairs or have theequipment repaired by a Grass-Telefactor service representative. After repair,test the complete system to verify that it complies with the publishedspecifications.Warning Do not open or remove the covers of the components. Anoperator may only perform maintenance procedures specificallydescribed in this manual. Refer servicing to qualified servicepersonnel trained in the repair of this equipment.Detailed circuit diagrams, components part lists, mechanical drawings, etc. areavailable for service purposes on formal request from Grass-Telefactor.
B-2 Chapter B Service Policy & Warranty

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