Connex® Spot Monitor Directions for use
© 2015 Welch Allyn. All rights are reserved. To support the intended use of the product described in this publication, the purchaser of the product is permitted to copy this publication, for internal distribution only, from the media provided by Welch Allyn. No other use, reproduction, or distribution of this publication, or any part of it, is permitted without written permission from Welch Allyn.
iii Contents Introduction ............................................................................................. 1 Intended use ........................................................................................................ 1 Contraindications ................................................................................................. 1 Symbols and definitions ......................................................................... 3 About warnings and cautions .....................
iv Contents Connex® Spot Monitor Alarm limits ........................................................................................................ 47 Alarm reminder signal ........................................................................................ 47 Alarm types ........................................................................................................ 47 Alarm notification locations ................................................................................
Directions for use Contents v Guidance and manufacturer's declaration ........................................ 143 EMC compliance .............................................................................................. 143 Emissions and immunity information ............................................................... 143 Appendices .......................................................................................... 147 Approved accessories ...............................................
vi Contents Connex® Spot Monitor
1 Introduction This manual describes the capabilities and operation of the Connex Spot Monitor (monitor). The information, including the illustrations, pertains to a monitor configured with noninvasive blood pressure (NIBP), body temperature, pulse oximetry (SpO2), and pulse rate. If your monitor configuration lacks any of these options, some information in this manual might not apply. Before using the monitor, read the sections of the manual that pertain to your use of the monitor.
2 Introduction Connex® Spot Monitor
3 Symbols and definitions Documentation symbols WARNING The warning statements in this manual identify conditions or practices that could lead to illness, injury, or death. Warning statements appear with a grey background in a black and white document. CAUTION The caution statements in this manual identify conditions or practices that could result in damage to the equipment or other property, or loss of data. This definition applies to both yellow and black and white symbols.
4 Connex® Spot Monitor Symbols and definitions Rated power input, DC Rated power input, AC Lithium-ion battery Direct current (DC) Connectivity symbols Bluetooth® Ethernet RJ-45 USB Nurse call Wireless signal strength • Best (4 bars) • Good (3 bars) • Fair (2 bars) • Weak (1 bar) • No signal (no bars) • No connection (blank) Miscellaneous symbols Manufacturer Defibrillation-proof Type BF applied parts Product Identifier Serial number Reorder number China RoHS markings for control of polluti
Directions for use Symbols and definitions 5 Light below FCC ID IPX1 Prescription only The identification number assigned by the Federal Trade Commission IC ID Industry Canada identification number.
6 Symbols and definitions Connex® Spot Monitor
7 About warnings and cautions Warning and caution statements can appear on the monitor, on the packaging, on the shipping container, or in this document. The monitor is safe for patients and clinicians when used in accordance with the instructions and the warning and caution statements presented in this manual. Before using the monitor, familiarize yourself with the sections of this directions for use that pertain to your use of the monitor.
8 About warnings and cautions Connex® Spot Monitor WARNING Patient injury risk. Any external compression of the blood pressure hose or cuff may cause patient injury, system errors, or inaccurate measurements. WARNING Patient injury risk. Wash hands to reduce the risk of crosscontamination and nosocomial infection. WARNING Patient injury risk. Do not place the monitor in any position that might cause it to fall on the patient. WARNING Patient injury risk.
Directions for use About warnings and cautions 9 WARNING Electric shock hazard. All signal input and output (I/O) connectors are intended for connection of only devices complying with IEC 60601-1, or other IEC standards (for example, IEC 60950), as applicable to the monitor. Connecting additional devices to the monitor may increase chassis or patient leakage currents. To maintain operator and patient safety, consider the requirements of IEC 60601-1-1.
10 Connex® Spot Monitor About warnings and cautions WARNING Liquids can damage electronics inside the monitor. Prevent liquids from spilling on the monitor. If liquids are spilled on the monitor: 1. 2. 3. 4. Power down the monitor. Disconnect the power plug. Remove battery pack from the monitor. Dry off excess liquid from the monitor. Note If liquids possibly entered the monitor, remove the monitor from use until it has been properly dried, inspected, and tested by qualified service personnel. 5.
Directions for use About warnings and cautions 11 CAUTION United States Federal law restricts this monitor to sale, distribution, or use by or on the order of a physician or licensed healthcare professional. CAUTION Electromagnetic interference risk. The monitor complies with applicable domestic and international standards for electromagnetic interference. These standards are intended to minimize medical equipment electromagnetic interference.
12 About warnings and cautions Connex® Spot Monitor
13 Controls, indicators, and connectors Your model might not contain all of these features. Note Front-Left view No. Feature Description 1 LCD screen 7" color touchscreen provides a graphical user interface. 2 Thermometry Secures the SureTemp unit to the monitor 3 Battery charge and power-up status indicator The LED indicates the charging and power-up status when connected to AC power: • Green: The battery is charged. • Amber: The battery is charging. • Flashing: the monitor is powering up.
14 Connex® Spot Monitor Controls, indicators, and connectors No.
Directions for use Controls, indicators, and connectors Back-Bottom-Left view 9 1 8 7 6 5 4 3 2 No.
16 Connex® Spot Monitor Controls, indicators, and connectors APM This section applies only to devices with an Accessory Power Management (APM) stand. The APM is an accessory stand with work surface, power supply for enhanced device run time, and organizational bins to arrange sensors and cables for available parameters. Front-Top-Left view 1 2 No.
Directions for use Controls, indicators, and connectors Back-Bottom-Right view 1 2 3 4 5 6 7 8 9 No.
18 Controls, indicators, and connectors Connex® Spot Monitor
19 Setup Supplies and accessories For a list of all approved supplies and accessories, see Approved Accessories in the Appendices. WARNING Patient injury risk. Clean all accessories, including cables and tubes, before storing the accessories on the device or cart. This helps reduce the risk of cross contamination and nosocomial infection. Refer to 'Clean the equipment' in "Maintenance and service" for directions. Connect the battery This procedure applies to first-time setup of the monitor.
Connex® Spot Monitor 20 Setup Mount the monitor The Connex Spot Monitor can be mounted on either the MS3 Connex Spot Classic Mobile Stand, Accessory Power Management (APM) stand, or wall mount. When mounted on an MS3 stand, a separate power supply is required. This power supply connects directly to the mains outlet. Follow the assembly instructions or directions for use included with your stand or wall mount. If you have an APM stand, follow all instructions regarding the equipotential terminal.
Directions for use Setup Connect AC power to MS3 Classic stand and monitor This section applies only to devices with Classic (MS3) stands. 1. Thread the power cable from the power supply through one of the spaces next to the pole to reach the monitor. 2. Attach the power supply to the underside of the basket using the 2 Phillips screws provided. 3. Connect the power cable to the monitor. 4. Connect the power cord to the mains outlet. 5. Power up the monitor.
22 Connex® Spot Monitor Setup Remove the temperature probe and probe well Follow these steps to disconnect the probe cable and remove the probe well. 1. On the underside of the probe well, press the spring tab on the SureTemp probe connector and pull it out of the probe well. 2. Remove the SureTemp probe from the probe well. 3. Grasp the probe well and pull it up to remove it from the monitor. Connect the NIBP hose 1. Place your thumb and forefinger on the hose connector spring tabs and squeeze firmly.
Directions for use Setup 23 CAUTION Connect cables in a manner that minimizes entangling. Detach an accessory To detach an accessory from the monitor, follow the instructions that accompanied the accessory. Disconnect AC power CAUTION Never move the monitor or mobile stand by pulling on any of the cords. This may cause the monitor to tip over or damage the cord. Never pull on the power cord when disconnecting the cord from the mains outlet.
24 Setup Connex® Spot Monitor
25 Startup Power The Power button, located on the lower-left corner of the monitor, performs multiple functions. • Powers up the monitor • Wakes the monitor from Sleep mode • Opens a pop-up dialog with controls to sign out, power down, and enter Sleep mode (except when an alarm condition is active) CAUTION Do not use a long press of the Power button to power down the monitor when it is functioning normally. You will lose patient data and configuration settings.
26 Connex® Spot Monitor Startup Type of alert Color Low Alarm Steady amber Very Low Alarm Cyan Information message Blue WARNING Steady amber indicates a low-level alarm. Flashing amber indicates a medium-level alarm. Flashing red indicates a high-level alarm. WARNING Always observe the monitor during power-up.
Directions for use Startup Image Description Bluetooth icon appears in Status area Bluetooth radio is ON Bluetooth icon is blinking on / off slowly The monitor is pairing with the laptop Bluetooth icon is blinking on / off quickly The monitor is connecting with the laptop Bluetooth icon appears with a border around the icon in the Status area The monitor and the laptop are connected and the monitor is ready to transmit data 27 In order to transmit data, you must first pair and then connect the
28 Connex® Spot Monitor Startup 3. Repeat the process as needed, or touch Cancel to dismiss the Bluetooth connection screen. Rename a laptop You can rename a paired laptop from a system or generic name to a specific name. 1. Select the arrow button to the right of the laptop name you want to edit in the paired list. A screen appears that allows you to change the laptop name to a preferred name. 2. Enter the name, and then touch Save. The new name appears in the list of paired devices.
Directions for use Startup 29 4. Touch one of the options. The monitor will either sign you out as a clinician so that another clinician can sign in, power down, go into Sleep mode, or return to the prior screen, depending on the option you choose. The battery continues to charge when in Sleep mode. Reset the monitor 1. If the monitor stops functioning, press and hold of the monitor, to reset the monitor. , located on the lower-left corner 2.
Connex® Spot Monitor 30 Startup Exit Sleep mode 1. Press either or tap the screen. The Login dialog box appears. 2. If you are the current user and are in a facility-specific login format, use the scanner or keypad to enter your ID and password. If you are logging back into the monitor, the monitor returns to the screen that previously was visible, keeps the patient's context, and maintains the vital signs that could have been previously captured. 3.
Directions for use Startup 31 The Clinician ID appears in the Clinician ID field on this tab and in the Status area on the Home tab. Use a barcode scanner The monitor enables the scanning of patient and clinician barcodes to enter ID information. The barcode scanner (scanner) supports linear and two-dimensional barcodes. If you have not done so previously, use the instructions provided with the scanner to attach the scanner to the monitor.
32 Connex® Spot Monitor Startup • WiFi and ethernet capability Office profile The Office profile is optimized for ambulatory vitals capture with external patient context and optional Bluetooth® functionality.
Directions for use Startup Intervals profile The Intervals profile is optimized for unattended episodic interval monitoring of a single patient with single patient review and alarms.
34 Connex® Spot Monitor Startup Profile feature comparison The monitor offers multiple profiles, including Spot, Office, and Interval. Profile feature comparison The following table compares the features of the profiles.
Directions for use Startup 35 Select a profile from the log in area If your facility has configured the Connex Spot Monitors with a facility-specific format, the Log in screen appears when the monitor is powered up 1. Sign in to the monitor. The Profile selection screen appears and displays up to three profiles. 2. Touch the desired profile. The Home tab appears for the chosen profile.
36 Connex® Spot Monitor Startup Icon Description OK key captures entered data and closes keypad or keyboard being used to enter data. Cancel key closes the keypad or keyboard without capturing entered data. Alpha key in the upper-left corner returns the keyboard to the basic alpha layout. Symbol key in the upper-left corner changes the keyboard from the basic alpha layout to the symbols and special characters layout.
Directions for use Startup 37 Item Description 3 Primary navigation Based on which profile is in use, the primary navigation tabs for that profile appear at the bottom of the screen. Battery status The battery status indicator displays the state of the battery. The battery status is represented by icons in the upper-right corner of the monitor display. The status represents several possible situations. • The monitor is connected to a power source and the battery is charging or is fully charged.
38 Connex® Spot Monitor Startup Alarm and information messages The Device Status area provides alarm and information messages that are either temporary or exist as long as the condition to which the message applies remains. Alarm or information messages may also include controls or behavior that you can use to manage alarm and information messages. When the monitor detects an alarm condition, the vitals frame relating to the alarm flashes and an alarm message appears.
Directions for use Startup 39 Manual entry and parameter modifiers You can change parameters manually by toggling between parameter values or using a pop-up screen to enter specific values. Change a parameter unit The units of measure for NIBP can be manually changed on the Home tab. Touch the NIBP frame. The NIBP changes between SYS/DIA and MAP. Note An authorized person can change the temperature unit of measure in Advanced settings. Change a frame manually 1. Press and hold a frame, such as NIBP.
40 Connex® Spot Monitor Startup • Patient • Alarms • Review • Settings Vertical tabs The vertical tabs on the left side of the screen enable you to navigate to additional areas of a primary tab. The vertical tabs displayed are determined by the primary tab chosen. Command buttons Command buttons, such as the Start Intervals button, enable you to navigate and perform actions. Shortcuts Shortcuts provide an efficient means of navigation.
Directions for use Startup 41 Alarms tab The Alarms tab contains vertical tabs. • General • NIBP • Pulse rate • SpO2 • Temperature. The General tab contains parameter controls for alarm limits, volume controls, audio controls, and alarm reset. Review tab The Review tab displays patient data that has been previously captured. Data can be viewed for a single patient or for multiple patients. The Review tab displays both core and custom parameters and also provides controls.
42 Startup Connex® Spot Monitor
43 Patient data management Patient data is managed through the Patient tab. From the Patient tab, you can do the following: • Scan a patient ID with the barcode scanner and return an Admit/Discharge/Transfer (ADT) patient name match. • Enter additional patient information. WARNING Patient injury risk. To ensure data integrity and patient confidentiality, save readings and clear the monitor's display between patients.
44 Connex® Spot Monitor Patient data management Add a patient Note This option is available in the Spot and Intervals profiles. 1. Touch the Patient tab. 2. Touch in any field and then enter patient information. 3. Touch Next to cycle through the patient data fields. Note You can use a barcode scanner to enter a patient ID in the Patient ID field. Touch the barcode, and touch OK. in the Patient ID field, scan 4. Touch OK to save and return to the Home tab.
Directions for use Patient data management Note You can configure the Intervals profile, to automatically send measurements to the network. Note Patient measurements older than 24 hours are automatically deleted from the patient records list on the Review tab. Note Modifying the date and time on the device modifies the date and time on all saved readings on the device. 45 Modifiers The Modifiers tab enables you to enter additional information for current measurements. Set modifiers 1.
46 Patient data management Connex® Spot Monitor
47 Alarms The monitor presents physiological alarms and technical alarms. Physiological alarms occur when vital sign measurements fall outside of set alarm limits, but they occur only in the Intervals profile. Technical alarms occur in all profiles. If the alarm system is powered down, the alarm log is maintained on the monitor for 14 days. Note The three modes of data communication—USB, Ethernet, and IEEE 802.11 —are not intended for real-time alarms.
48 Connex® Spot Monitor Alarms Type • Priority Color Alarm audio tone Some technical alarms Alarm notification locations WARNING Patient injury risk. If you are relying on visual alarm notifications, maintain a clear line of sight with the monitor and/or Nurse Call. Set the volume as needed considering the environment and ambient noise levels. WARNING Patient injury risk. Do not set the alarm parameters to extreme levels.
Directions for use Alarms 49 Icons in parameter frames Icon Name and status Alarm off. No visual or audio alarms or Nurse Call notification will occur for this parameter. Alarm on. Audio and visual notifications and Nurse Call are enabled. Alarm audio off. Only visual notifications, including Nurse Call, will occur. Alarm audio paused. The default audio pause alarm duration is 1 minute. The icon remains until the paused time counts down to 0. Authorized personnel can configure this parameter.
50 Connex® Spot Monitor Alarms Reset (pause or turn off) audio alarms Audio alarm characteristics • After you reset an audio alarm, some tones do not return, but others return after a pause interval if the condition that caused the alarm persists. Settings in the Advanced tab determine the length of the pause interval. • If a new alarm condition occurs during a pause interval, a new audio tone occurs. Pause or turn off an audio alarm 1. In the Device Status area, touch .
Directions for use Alarms 51 Adjust vital sign alarm limits You can adjust vital sign alarm limits or turn off alarm limit checking for individual parameters. WARNING Alarm limits are user adjustable. All alarm limit settings should take into account the patient's condition and acute care needs. Appropriate alarm limits should be set accordingly for each patient. CAUTION Loss of power will cause the monitor to return to default settings.
52 Connex® Spot Monitor Alarms If you turn off audio alarms, visual alarm signals still occur in the Device Status area and on the Home tab in parameter frames. The in the Device Status area indicates alarm audio turned off, and a similar bell will appear in the parameter frames . If an alarm condition occurs, the bell will be red or amber in the alarming frame, according to the priority of the alarm, as shown here: • or .
Directions for use Alarms Alarm messages Priority Alarm limit exceeded. SpO2 LOW. High Alarm limit exceeded. Temperature HIGH. High Alarm limit exceeded. Temperature LOW. High 53 Nurse Call The monitor can be connected to a Nurse Call system through a cable that connects to the Nurse Call connector. When the Nurse Call cable is connected and Nurse Call is enabled, the monitor immediately notifies the Nurse Call system when any alarm condition occurs that exceeds the preset threshold.
54 Alarms Connex® Spot Monitor
55 Patient monitoring Required parameters If a parameter is required, a Skip button appears at the bottom of the parameters, and a Next button appears in the lower-right corner of the screen. Parameters may require three types of inputs. • Numerics • Drop-down lists • Parameter option buttons If you choose not to record information for the parameter, a dialog box appears to confirm that the parameter is not being recorded.
56 Connex® Spot Monitor Patient monitoring 3. Proceed to the second and third parameters and enter the required information either manually or enter the data with the format presented. 4. If there is a required parameter that you choose not to complete, then touch Skip. An override dialog box appears explaining that it is a required parameter and the EMR will note that it was not captured. 5. Touch Cancel, return and complete the parameter, or touch OK to continue to the next parameter. 6.
Directions for use Patient monitoring 57 WARNING Patient harm risk. Do not use intervals on neonates out of your hearing range. Verify that the audio can be heard from where you intend to be. Automatic intervals You can configure the monitor to take automatic NIBP measurements at consistent intervals. Note An alarm does not turn off intervals. Subsequent automatic measurements continue to occur as scheduled. Start Automatic intervals 1. Place the proper cuff around the patient’s bare upper arm. 2.
58 Connex® Spot Monitor Patient monitoring Stat intervals You can configure the monitor to take NIBP measurements continuously. When you select Stat on the Intervals tab in Settings, the monitor takes repeated NIBP measurements for 5 minutes, starting a new cycle each time the cuff deflates below safe venous return pressure (SVRP) for 2 seconds. WARNING Patient injury risk.
Directions for use Patient monitoring 59 NIBP NIBP measurements WARNING Patient injury risk. Do not install luer connectors on blood pressure tubing. Using luer connectors in manual or automated blood pressure systems creates the risk of inadvertent connection to intravenous (IV) tubing, which can introduce air into the patient’s circulatory system. WARNING Patient injury risk. Any external compression of the blood pressure hose or cuff may cause patient injury, system errors, or inaccurate measurements.
60 Connex® Spot Monitor Patient monitoring For information about obtaining blood pressure measurements, refer to Blood pressure guidelines at www.welchallyn.com/. NIBP measurement display In all profiles, the frame can display systolic and diastolic measurements, and MAP calculations. Authorized personnel can configure the default view in Advanced settings. The last NIBP measurement remains on the screen unless you touch Save or Clear, or until a new measurement is taken.
Directions for use Patient monitoring 61 Obtain a single NIBP measurement 1. Touch START to begin a single measurement. The START button becomes an orange STOP button. NIBP always displays the current inflation rate. When complete, the NIBP parameter displays the completed NIBP measurement. 2. Touch Save to save the displayed measurement in the patient's record The measurement will continue to be displayed until you save it or you start another NIBP measurement.
62 Connex® Spot Monitor Patient monitoring Temperature Configure temperature alarms You must be in the Intervals profile to set alarm limits. 1. Touch the Alarms tab. 2. Touch the Temperature vertical tab. 3. Using either the keypad or ▲ or ▼, enter the desired upper and lower alarm limits. 4. Touch the Home tab. The new alarm settings appear in the Alarm Limit control button.
Directions for use Patient monitoring 63 Site selection Remove the temperature probe and touch the Temperature site control to toggle between sites. Icon Description Pediatric axillary Adult axillary Oral Rectal. Monitors configured with the temperature module and the red rectal probe well and probe default to the rectal mode. Ear mode. The monitor displays the ear mode when it receives a temperature measurement from the ear thermometer.
64 Connex® Spot Monitor Patient monitoring Temperature buttons The buttons on the right side of the frame enable you to perform different tasks, depending on the profile you are using. The profile you choose determines which functions are available. Icon Button name Description Temperature alarm Displays alarm limits and status. Touch the button to display the Alarms tab. Direct mode Touch the button to enter Direct mode.
Patient monitoring Directions for use 65 WARNING Never use a damaged temperature probe. The thermometer consists of high-quality precision parts and should be protected from severe impact or shock. Do not use the thermometer if you notice any signs of damage to the probe or monitor. If the thermometer probe is dropped or damaged, remove it from use and have it inspected by qualified service personnel. WARNING Inaccurate measurement risk.
66 Connex® Spot Monitor Patient monitoring CAUTION The monitor does not retain Direct mode temperatures in memory unless there is a physiological temperature alarm condition. If there is a physiological temperature alarm condition, the monitor automatically saves the measurement in the patient record.
Directions for use Patient monitoring • Remove the probe from the probe well, load a probe cover, select a temperature site, and expose the probe to ambient air for more than 60 seconds. The temperature frame changes to "MODE: Direct...". • If you have a patient whose body temperature is below the normal temperature range and you follow the previous step, the probe sensor identifies this condition and turns off the probe preheater in order to accommodate the lower body temperature measurement.
68 Connex® Spot Monitor Patient monitoring Take a temperature at the rectal site WARNING Patient injury risk. When taking rectal temperatures, insert the probe tip only 5/8 inch (approximately 1.5 cm) inside the rectum of adults and only 3/8 inch (approximately 1 cm) inside the rectum of children to avoid the risk of bowel perforation. WARNING Cross-contamination or nosocomial infection risk. Thorough hand-washing greatly reduces the risk of cross-contamination and nosocomial infection.
Directions for use Patient monitoring 69 Braun ThermoScan® PRO 6000 thermometer The Braun ThermoScan Pro 6000 thermometer enables you to transfer an ear temperature measurement to the monitor. Read the thermometer manufacturer's directions for use before attempting to configure, use, troubleshoot, or maintain the thermometer. WARNING Liquids can damage electronics inside the thermometer. Prevent liquids from spilling on the thermometer.
70 Connex® Spot Monitor Patient monitoring CAUTION Inaccurate measurement risk. If ear drops or other ear medications have been placed in one ear canal, take the temperature in the untreated ear. Note A temperature measurement taken in the right ear might differ from a measurement taken in the left ear. Therefore, always take the temperature in the same ear. Note When the monitor receives an ear temperature measurement, it displays the measurement on the Home tab.
Directions for use Patient monitoring 71 1. Place the thermometer in the accessory dock. 2. Make sure that the monitor is connected to AC power. 3. Make sure that the monitor is powered on. The LED on the dock indicates the charging status of the battery pack: • Orange: The battery pack is charging. • Green: The battery pack is charged. • Not illuminated: The battery pack is not charging. Note The battery pack continues to charge while the monitor is in Display power saving mode.
72 Connex® Spot Monitor Patient monitoring and varies between monitoring sites and from patient to patient, as physiological conditions vary. Masimo displays the LofP as a numeric value and refers to it as Perfusion Index. Nonin displays the LofP as a color value (yellow or red) only when the LofP is low, based on the sensor's algorithm. During sensor placement, the LofP can be used to evaluate the appropriateness of an application site by looking for the site with the highest LofP number.
Directions for use Patient monitoring 73 WARNING Inaccurate measurement risk. Severe anemia may cause erroneous SpO2 readings. WARNING Inaccurate measurement risk. The pulse oximeter can be used during defibrillation, but the readings may be inaccurate for up to 20 seconds. WARNING Inaccurate measurement risk. Misapplied sensors or sensors that become partially dislodged may cause either over or under reading of actual arterial oxygen saturation. WARNING Inaccurate measurement risk.
74 Connex® Spot Monitor Patient monitoring WARNING Use the pulse oximeter as an early warning device. As you observe a trend toward patient hypoxemia, use laboratory instruments to analyze blood samples to better understand the patient's condition.
Directions for use Patient monitoring 75 CAUTION Do not modify or alter the sensor in any way. Alterations or modification may affect performance and/or accuracy. 1. Verify that the sensor cable is connected to the monitor. WARNING Patient injury risk. The sensor and extension cable are intended only for connection to pulse oximetry equipment. Do not attempt to connect these cables to a PC or any similar device. Always follow the sensor manufacturer's directions for care and use of the sensor. 2.
76 Connex® Spot Monitor Patient monitoring WARNING Inaccurate measurement risk. Pulse rate measurements generated through the blood pressure cuff or through SpO2 are subject to artifact and might not be as accurate as heart rate measurements generated through ECG or manual palpation. Configure pulse rate alarms You must be in the Intervals profile to configure the pulse rate alarms. 1. Touch the Alarms tab. 2. Touch the Pulse rate vertical tab. 3.
Directions for use Patient monitoring 77 Enter manual parameters Note Authorized personnel can select and configure the Manual parameters frame in Advanced settings. Only four parameter types appear in the Manual parameters frame. 1. On the Home tab, press and hold the parameter desired. 2. Using either the keypad or ▲ or ▼, manually enter information for the parameter chosen. Ensure that the current patient ID is correct before saving. Note 3. Touch Ok to capture the parameter that you entered.. 4.
78 Patient monitoring Connex® Spot Monitor
79 Maintenance and service Perform periodic checks 1. Verify the following at least daily. • The audio speaker tone, especially at startup • The touchscreen alignment • The date • The time 2. Visually inspect the following at least weekly.
80 Connex® Spot Monitor Maintenance and service 4. Remove the old battery from the battery compartment. 5. Disconnect the battery connector from the battery connection port on the monitor. 6. Insert the battery connector for the new battery into the battery connection port on the monitor. 7. Insert the new battery into the battery compartment. 8. Replace the battery cover, and then tighten the captive screw at the bottom of the battery cover. Note Do not overtighten the screw.
Directions for use Maintenance and service 81 3. Gently lift the latch with one hand and pull the tab on the top of the battery with your other hand to remove the battery from its slot. 4. Slide the new battery into the slot. Note Ensure that the tab is facing you on the top of the battery. 5. Replace the battery cover and tighten the captive screw on the bottom of the APM work surface.
82 Connex® Spot Monitor Maintenance and service CAUTION Do not sterilize the monitor. Sterilizing the monitor could harm the device. If liquids are spilled on the monitor: 1. 2. 3. 4. Power down the monitor. Disconnect the power cord from the mains outlet and the power source. Remove battery pack from the monitor. Dry off excess liquid from the monitor.
Directions for use Maintenance and service 83 Section 2.
84 Connex® Spot Monitor Maintenance and service WARNING Electric shock hazard. Do not open the monitor or attempt repairs. The monitor has no user-serviceable internal parts. Only perform routine cleaning and maintenance procedures specifically described in this manual. Inspection and servicing of internal parts shall only be performed by qualified service personnel. CAUTION Sterlizing the monitor could damage the device. 1. Disconnect the AC power cord from the mains outlet. 2.
Directions for use Maintenance and service 2. Remove the thermometer from the dock and clean the metal electrical contacts on the thermometer with the cotton swab. 3. Place the thermometer aside for 1 minute, allowing the contacts to air dry. 4. Clean the metal electrical contacts on the device dock with the cotton swab. 5. Allow the contacts to air dry for 1 minute. 6. Optional step to improve performance: On the dock only, apply DeoxIT Gold® to the tip of each electrical contact.
86 Maintenance and service Connex® Spot Monitor
87 Troubleshooting This section presents tables of technical alarm and information messages, as well as problem descriptions that do not generate messages, to help you troubleshoot issues on the monitor. Note Problem descriptions without messages appear at the end of this section. When the monitor detects certain events, a message appears in the Device Status area at the top of the screen. Below are the message types. • Information messages, which appear on a blue background.
88 Connex® Spot Monitor Troubleshooting Message Possible cause Unable to determine NIBP; check connections; limit patient movement. 050003 The NIBP measurement may be Make sure the NIBP settings/patient Medium inaccurate, patient motion mode is appropriate. If the problem occurred, or the settings for persists, replace the module. patient readings obtain might not be accurate Unable to determine NIBP; check connections; limit patient movement.
Directions for use Troubleshooting Message Possible cause Suggested action Alarm priority patient movement. 05000F NIBP not functional. 050105 WACP message CRC mismatch on Internal malfunction. If the problem NIBP module persists, replace the module. Very low NIBP not functional. 050201 This message is not implemented Internal malfunction. If the problem by the NIBP module persists, replace the module. Very low NIBP not functional. 050202 This message is not supported by Internal malfunction.
90 Connex® Spot Monitor Troubleshooting Message Possible cause Suggested action Alarm priority Invalid algorithm. Select Invalid NIBP Algorithm. NIBP correct algorithm and component software tried to retry. 05050A configure the sensor in an illegal manner Verify the algorithm. If the problem persists, replace the module. Very low NIBP not functional. 050513 Internal malfunction. If the problem persists, replace the module. Very low Invalid NIBP initiation code Invalid patient mode.
Directions for use Troubleshooting Message Possible cause Suggested action Alarm priority Stat mode requested too NIBP excessive stat mode time. Internal malfunction. If the problem soon. Clear to retry. The time between readings is less persists, replace the module. 050609 than one minute and the readings plus time between readings result in the device taking over 15 minutes to complete the averaging cycle.
92 Connex® Spot Monitor Troubleshooting Message Possible cause Suggested action Alarm priority Check cuff inflation settings. Cuff inflation target was overridden due to max pressure being too low Change cuff inflation target or maximum pressure so that the cuff inflation target is at least 20 mmHg lower than maximum pressure. Information Tube type does not match device configuration.
Directions for use Troubleshooting Message Possible cause Suggested action Alarm priority Tube type does not match device configuration. The tube type settings and the actual tube type do not match Change the tube type setting to match the actual tube type. Information SpO2 messages General SpO2 messages Message Possible cause Suggested action Alarm priority SpO2 not functional. 044800 The SpO2 power on self test failed Internal hardware malfunction in SpO2 module. Replace the module.
94 Connex® Spot Monitor Troubleshooting Message Possible cause Suggested action Alarm priority tester. If the message persists, replace the module. Replace the SpO2 cable. The SpO2 cable is incompatible 040800 with the monitor Replace the SpO2 cable. If the Very low problem is still present, verify module functionality by replacing the sensor with an applicable SpO2 tester. If the message persists, replace the module. Replace the SpO2 cable. The SpO2 cable is not recognized Replace the SpO2 cable.
Directions for use Troubleshooting Message Possible cause Suggested action Alarm priority Replace the SpO2 sensor. 040f00 The SpO2 sensor is defective Replace SpO2 sensor. If the problem Very low is still present, replace the SpO2 cable. If the problem is still present, verify the module functionality by replacing the sensor with an applicable SpO2 tester. If the message persists, replace the module. Replace the SpO2 sensor. Replace the SpO2 cable.
96 Connex® Spot Monitor Troubleshooting Message Possible cause Suggested action Alarm priority applicable SpO2 tester. If the message persists, replace the module. Searching for pulse signal. 041800 SpO2 pulse search Pulse search is part of normal operation, and does not have an associated corrective action. Low perfusion index. Clear to retry. 041a00 There is marginal SpO2 pulse quality or artifact. Reapply the sensor to the patient.
Directions for use Troubleshooting Message Possible cause Suggested action Alarm priority the board is out of specification. In this case, the failure may be cleared once the underlying cause is removed. Second, the board has an actual hardware failure and recovery is not possible. It is recommended that the SpO2 module be replaced, and if problem is still present replace the monitor's main board. SpO2 rebooting. 042100 There is an SpO2 watchdog failure A malfunction is detected.
98 Connex® Spot Monitor Troubleshooting Message Possible cause SpO2 rebooting. 042500 There is an SpO2 SRAM task queue overrun Suggested action Alarm priority A malfunction is detected. There are Very low two possible causes of these failures. First, the power provided to the board is out of specification. In this case, the failure may be cleared once the underlying cause is removed. Second, the board has an actual hardware failure and recovery is not possible.
Directions for use Troubleshooting Message Possible cause Suggested action Alarm priority that the SpO2 module be replaced, and if problem is still present replace the monitor's main board. SpO2 rebooting. 042a00 There is a problem with the SpO2 A malfunction is detected. There are Very low LED ground two possible causes of these failures. First, the power provided to the board is out of specification. In this case, the failure may be cleared once the underlying cause is removed.
100 Connex® Spot Monitor Troubleshooting Message Possible cause Suggested action Alarm priority removed. Second, the board has an actual hardware failure and recovery is not possible. It is recommended that the SpO2 module be replaced, and if problem is still present replace the monitor's main board. SpO2 rebooting. 042f00 There is a problem with the SpO2 A malfunction is detected. There are Very low positive detector voltage two possible causes of these failures.
Directions for use Troubleshooting Message Possible cause Suggested action Alarm priority the board is out of specification. In this case, the failure may be cleared once the underlying cause is removed. Second, the board has an actual hardware failure and recovery is not possible. It is recommended that the SpO2 module be replaced, and if problem is still present replace the monitor's main board. SpO2 rebooting. 043400 There is a problem with the SpO2 A malfunction is detected.
102 Connex® Spot Monitor Troubleshooting Message Possible cause Suggested action Alarm priority SpO2 rebooting. 044200 The SpO2 module received a bad packet There is an internal software Very low malfunction in the main PCBA. Update the software. If the problem persists, replace the module. SpO2 rebooting. 044300 The SpO2 module received an invalid command There is an internal software Very low malfunction in the main PCBA. Update the software. If the problem persists, replace the module.
Directions for use Troubleshooting Message Possible cause Suggested action Alarm priority SpO2 rebooting. 043d00 SpO2 module hardware error A module hardware error is detected. Replace module. Very low SpO2 rebooting. 043e00 SpO2 module software error A module hardware error is detected. Replace module. Very low SpO2 rebooting. 043f00 The SpO2 module received a bad message This error indicates a bug in the main Very low board software. Call for service. Replace the SpO2 sensor.
104 Connex® Spot Monitor Troubleshooting Message Possible cause Suggested action Alarm priority tester. If the message persists, replace the module. 1Pulse search is a normal part of operation and does not have an associated corrective action. Temperature messages SureTemp messages Message Possible cause Suggested action Alarm priority Temperature not functional. 30105 WACP message CRC mismatch on temperature module Internal malfunction. If the problem persists, replace the module.
Directions for use Troubleshooting Message Possible cause Suggested action 105 Alarm priority module state prohibits the request/action. Temperature not functional. 3020B The temperature Internal malfunction. If the problem module requested item persists, replace the module. is not currently available due to the module state. Very low Temperature not functional. 30503 The temperature Internal malfunction. If the problem module factory persists, replace the module.
106 Connex® Spot Monitor Troubleshooting Message Possible cause Suggested action Alarm priority ambient or patient limits. Temperature not functional. 30803 The temperature module internal calibration resistor (RCAL) on the board is damaged or contaminated (pulse too long). Internal malfunction. If the problem persists, replace the module. Very low Temperature not functional.
Directions for use Troubleshooting Message Possible cause Suggested action Alarm priority detection mechanism detected an error Temperature not functional. 3080D The temperature module log error detection mechanism detected an error Probe malfunction. Replace probe. If the problem persists, replace the module. Very low Temperature not functional. 3080E The temperature Probe malfunction. Replace probe. If the module calibration error problem persists, replace the module.
108 Connex® Spot Monitor Troubleshooting Message Possible cause Suggested action Alarm priority Probe malfunction. Replace probe. If the problem persists, replace the module. Very low indicates on when turned off. Unable to detect new The temperature temperature. Retry measurement. module heater 30819 indicates off when turned on. Temperature not functional. 3081A The temperature Internal malfunction. If the problem module HTR_Q is on persists, replace the module.
Directions for use Troubleshooting 109 Message Possible cause Suggested action Alarm priority Temperature not functional. 30825 The temperature module is under min battery volts Internal malfunction. If the problem persists, replace the module. Very low Temperature not functional. 30826 The temperature module battery volts not set Internal malfunction. If the problem persists, replace the module. Very low Temperature not functional.
110 Connex® Spot Monitor Troubleshooting Message Possible cause Suggested action Alarm priority Temperature not functional. 03CE01 Upgrade file directory could not be accessed Retry the device update Very low Direct mode reading timed out Direct mode reading times out Direction mode reading times out Information Tissue contact lost. Lost tissue contact Check the tissue contact and try the while attempting to measurement again.
Directions for use Troubleshooting Suggested action Alarm priority Message Possible cause Temperature not functional. 3F0208 The object provided Internal malfunction. If the problem with the message could persists, replace the module. not be deserialized. Very low Temperature not functional. 3F0209 The object could not be Internal malfunction. If the problem serialized. persists, replace the module. Very low Temperature not functional. 3F020A The message is Internal malfunction.
112 Connex® Spot Monitor Troubleshooting Possible cause Temperature not functional. 3F0824 The battery is over the Internal malfunction. If the problem maximum voltage persists, replace the module. Very low Temperature not functional. 3F0833 The sensor not functional Internal malfunction. If the problem persists, replace the module. Very low Temperature not functional. 3F0E04 Low battery Recharge the battery. If the problem persists, check the battery.
Directions for use Troubleshooting 113 Alarm priority Message Possible cause Suggested action Unable to identify clinician. Invalid ID or system password. Clinician authentication failure Information status message; press OK button Information to dismiss. Unable to identify clinician. Account disabled/expired. Clinician authentication failure Information status message; press OK button Information to dismiss. Unable to identify clinician. Password expired/reset required.
114 Connex® Spot Monitor Troubleshooting Alarm priority Message Possible cause Suggested action Clinician ID required to start intervals. A Clinician ID is required to start intervals Information status message; press OK button Information to dismiss. Patient ID match required to save data. A Patient ID match is required to save data N/A Information Patient ID match required to start intervals.
Directions for use Troubleshooting Alarm priority Message Possible cause Suggested action Radio not functional. 350002 Permissions. There is an internal software error on the radio Check for a software update and apply it. Very low If still present, replace the radio. Radio not functional. 350003 Unsupported operating system. Check for a software update and apply it. Very low There is an internal software error If still present, replace the radio. on the radio Radio not functional.
116 Connex® Spot Monitor Troubleshooting Alarm priority Message Possible cause Suggested action Radio not functional. 350010 Missing interface. There is an internal software error on the radio indicating a Linux kernel error or failure to initialize the network interface Check for a software update and apply it. Very low If still present, replace the radio. Radio not functional. 350011 Unknown interface.
Directions for use Troubleshooting Alarm priority Message Possible cause Suggested action Radio not functional. 35001f Invalid power mode. There is an internal software error on the radio Check for a software update and apply it. Very low If still present, replace the radio. Radio not functional. 350020 Post results missing. There is an internal software error on the radio Check for a software update and apply it. Very low If still present, replace the radio. Radio not functional.
118 Connex® Spot Monitor Troubleshooting Alarm priority Message Possible cause Suggested action Radio not functional. 350033 Serialization failure. There is an internal software error on the radio or the monitor Check for a software update and apply it. Very low If still present, replace the radio. Radio not functional. 350034 Missing PAC file. There is a misconfiguration of the radio (configured for EAP-FAST and manual PAC but none supplied) Check the radio configuration.
Directions for use Troubleshooting Alarm priority Message Possible cause Suggested action Radio not functional. 350041 Unable to configure DHCP 60 on the radio Check the radio configuration. If the Very low problem is still present, reset the radio to factory defaults. If the problem persists, check for software update and apply it. If still present, replace the radio. Radio not functional. 350042 DHCP option corrupt.
120 Connex® Spot Monitor Troubleshooting Connectivity messages Message Possible cause Suggested action Alarm priority Unable to obtain wired device IP address. 210000 No wired connection Verify DHCP functionality and configuration. Very low Network not found; check network cable connection. 210100 Lost ethernet DHCP address Check wired connection into device then verifiy DHCP functionality and configuration. Very low Unable to communicate Cannot communicate with NRS with NRS.
Directions for use Troubleshooting Message Possible cause Suggested action 121 Alarm priority Error in record. Try again Connectivity NACK recieved for NRS/ECS/CS/NCE NRS/ECS/CS/NCE NACK that is record Information specific and can be fixed by a clinician in the next record Send successful.
122 Connex® Spot Monitor Troubleshooting Alarm priority Message Possible cause Suggested action Update unsuccessful. Reboot and retry. 1C1008 The software update failed Restart the monitor. If the problem is still present, replace the main PCBA. Host battery not charging. 1C100A The host battery is not charging Restart the monitor. If the problem is still Very low present, check cable connections. If the problem is still present, perform functional checks for host.
Directions for use Troubleshooting Suggested action 123 Alarm priority Message Possible cause Firmware update successful. The software successfully updated Information status message; press OK button to dismiss. Information Audio alarms are off. The monitor alarm audio is off Information status message; press OK button to dismiss. Information Advanced settings unavailable.
124 Connex® Spot Monitor Troubleshooting Message Possible cause Suggested action Alarm priority Software Update: Invalid token file. There was an invalid token file Verify and update the token file. Information Software Update: The manifest file was not found Unable to find manifest on the server file on server. Verify the manifest file is on the server. Information Software Update: The manifest file signature Unable to verify verification failed. manifest file signature.
Directions for use Troubleshooting 125 Message Possible cause Suggested action Alarm priority Bluetooth device connection successful The Bluetooth device connected None. Information Bluetooth device disconnected The Bluetooth disconnected None. Information Message Possible cause Suggested action APM not functional. 1C1001 The APM is detected as connected Restart the monitor and the APM.
126 Connex® Spot Monitor Troubleshooting Message Possible cause Suggested action Alarm priority message persists, replace the main PCBA on the monitor. APM not functional. 1C1004 The APM PIC cannot communicate Restart the monitor and the APM. If the Very low with the accelerometer problem is still present, check the cable connections from the monitor to APM. If the problem still present, replace APM. If the message persists, replace the main PCBA on the monitor. APM not functional.
127 Specifications Physical specifications Protection classifications, all monitor configurations Characteristic Specification Electrical rating 100 – 240 V AC, 50 – 60 Hz, 0.8X– 1.
128 Connex® Spot Monitor Specifications Protection classifications, all monitor configurations Graphical display resolution Dimensional outline 6.5 in. (W) x 4.1 in. (H) x 0.13 in. (D) (164.9 mm [H] x 103.8 mm [W] x 3.40 mm [D] ) Active area 6.1 in. (W) x 3.4 in. (H) (154.08 mm [W] x 85.92 mm [H]) Resolution 800 x 480 pixels Pixel arrangement RGB (red, green, blue) Pixel size 63.2 µm (W) x 179 µm (H) Luminance 530 cd/m2 Speaker volume Minimum Output sound pressure 60 dB at 1.
Directions for use Specifications 129 Hours of use 2 Cell battery specifications1 Acute care continuous 10 minute cycles - 49 patient cycles - BP, temp, SpO2, no radio, 8.22 no scanner (Nellcor) Acute care continuous 10 minute cycles - 50 patient cycles - BP, temp, SpO2, no radio, 8.37 no scanner (Nonin) Acute care continuous 10 minute cycles - 49 patient cycles - BP, temp, SpO2, no radio, 8.
130 Connex® Spot Monitor Specifications NIBP specifications Blood pressure determination time Typical: 15 seconds Maximum: 150 seconds Blood pressure accuracy Meets or exceeds ANSI.AAMI SP10:2002 standards for noninvasive blood pressure accuracy (±5 mmHg mean error, 8 mmHg standard deviation) Mean Arterial Pressure (MAP) range The formula used to calculate MAP yields an approximate value.
Directions for use Specifications 131 SpO2 specifications Refer to sensor manufacturer's directions for use for additional information. WARNING Functional testers cannot be used to assess the accuracy of a pulse oximeter monitor. While functional testers may be useful for verifying that the pulse oximeter sensor, cabling, and monitor are functional, they are incapable of providing the data required to properly evaluate the accuracy of a system's SpO2 measurements.
132 Connex® Spot Monitor Specifications SpO2 specifications (Masimo specifications, see footnotes 1, 2, 3, 4, 5, and 6) No motion: ± 3 digits Motion: ± 5 digits Saturation Note Saturation accuracy varies by sensor type. Refer to the sensor Directions for use for additional accuracy information.
Directions for use Specifications 133 SpO2 specifications (Masimo specifications, see footnotes 1, 2, 3, 4, 5, and 6) Finger Clip: ± 2 digits Flex: ± 3 digits Flex: ± 3 digits Soft Sensor: N/A Soft Sensor: ± 2 digits 8000R: N/A 8000R: ± 3 digits 8000 Q: N/A 8000 Q: ± 4digits Motion Motion Finger Clip: ± 3 digits Finger Clip: ± 2 digits Flex: ± 4 digits Flex: ± 3 digits Soft Sensor: ± 4 digits Soft Sensor: ± 3 digits Low Perfusion Low Perfusion All Sensors: ± 3 digits All Sensors: ± 2 d
134 Connex® Spot Monitor Specifications 7 Some models of commercially available bench-top functional testers and patient simulators can be used to verify the proper functionality of Nellcor pulse oximeter sensors, cables and monitors. See the individual testing device's operator's directions for use for the procedures specific to the model of tester being used.
Directions for use Specifications 135 802.11n (OFDM,HT20,MCS 0-7): 6.5,13,19.5, 26, 39,52, 58.5, 72.2 Mbps Agency approvals US: FCC Part 15.247 Subpart C, FCC Part 15.407 Subpart E Europe: EN 300 328 (EDR) (v1.8.1), EN 300 328 (LE) (v1.8.1), EN 301 489-1 (v1.9.2), EN 301 489-17 (v2.2.1), EN 301 489-17 (v2.2.1), EN 62311:2008, EN 60950-1 Canada: (IC) RSS-210 standard.
136 Connex® Spot Monitor Specifications GPIO Four configurable lines (1.8V/3.3V configurable by VDD_PADS HCI Host Controller Interface over USB HID proxy mode Human Interface Device EEPROM 2-wire 64K bits Coexistence 802.
137 Standards and compliance General compliance and standards The monitor complies with the following standards: 21 CFR Subchapter H – Medical Devices – US Food and Drug Administration 2002 No.
138 Standards and compliance Connex® Spot Monitor Electrical Equipment (WEEE). If this product is contaminated, this directive does not apply. For more specific disposal or compliance information, see www.welchallyn.com/weee, or contact Welch Allyn Customer Service at +44 207 365 6780. General radio compliance The wireless features of this monitor must be used in strict accordance with the manufacturer’s instructions as described in the user documentation that comes with the product.
Directions for use Standards and compliance 139 Industry Canada (IC) emissions This device complies with RSS 210 of Industry Canada. Operation is subject to the following two conditions: (1) this device may not cause interference, and (2) this device must accept any interference, including interference that may cause undesired operation of this device.
140 Standards and compliance Connex® Spot Monitor tout brouillage radioélectrique subi, même si le brouillage est susceptible d'en compromettre le fonctionnement. European Union Czech Welch Allyn tímto prohlašuje, ze tento RLAN device je ve shodě se základními požadavky a dalšími příslušnými ustanoveními směrnice 1999/5/ES.
Directions for use Standards and compliance 141 Spanish Por medio de la presente Welch Allyn declara que el RLAN device cumple con los requisitos esenciales y cualesquiera otras disposiciones aplicables o exigibles de la Directiva 1999/5/CE Swedish Härmed intygar Welch Allyn att denna RLAN device står I överensstämmelse med de väsentliga egenskapskrav och övriga relevanta bestämmelser som framgår av direktiv 1999/5/EG.
142 Standards and compliance Connex® Spot Monitor
143 Guidance and manufacturer's declaration EMC compliance Special precautions concerning electromagnetic compatibility (EMC) must be taken for all medical electrical equipment. This device complies with IEC EN 60601-1-2:2007. • All medical electrical equipment must be installed and put into service in accordance with the EMC information provided in this Directions for use. • Portable and mobile RF communications equipment can affect the behavior of medical electrical equipment.
144 Connex® Spot Monitor Guidance and manufacturer's declaration Electromagnetic emissions Voltage fluctuations/ flicker emissions IEC 61000-3-3 Complies WARNING This equipment/system is intended for use by healthcare professionals only. This equipment/ system may cause radio interference or may disrupt the operation of nearby equipment a. It may be necessary to take mitigation measures, such as re-orienting or relocating the monitor or shielding the location.
Directions for use Guidance and manufacturer's declaration 145 Electromagnetic immunity from the equation applicable to the frequency of the transmitter. Recommended separation distance Conducted RF IEC 61000-4-6 3 Vrms 150 kHz to 80 MHz 3 Vrms Radiated RF IEC 61000-4-3 3 V/m 80 MHz to 1 GHz 3 V/m d= (1.17) d= (1.17) 80 to 800 MHz d= (2.33) 800 MHz to 2,5 GHz whereP is the maximum output power rating of the transmitter in watts (W) andd is the recommended separation distance in meters (m).
146 Connex® Spot Monitor Guidance and manufacturer's declaration Recommended separation distances between portable and mobile RF communications equipment and the monitor 0.1 0.36894 0.36894 0.73785 1 1.1667 1.1667 2.3333 10 3.6894 3.6894 7.3785 100 11.667 11.667 23.
147 Appendices Approved accessories The following tables list approved monitor accessories and applied parts. For information about options, upgrades, and licenses, refer to the service manual. WARNING Use only Welch Allyn approved accessories and applied parts, and use them according to the manufacturer’s directions for use.
148 Connex® Spot Monitor Appendices Nellcor pulse oximetry Part number Model Description DS-100A OxiMax Durasensor adult oxygen transducer DOC-10 OxiMax Extension cable (10 feet) DOC-8 OxiMax Extension cable (8 feet) DOC-4 OxiMax Extension cable (4 feet) Nonin pulse oximetry Part number Model Description 6083-001 1m Nonin Extension Cable 6083-003 3m Nonin Extension Cable SureTemp Plus thermometry Part number Description 02895-000 Oral probe and well kit (9ft. / 2.
Directions for use Appendices 149 Mounting options Part number Description 7000-APM Accessory Power Management (APM) — organized mobile stand with battery and basket 7000-MS3 Connex Spot Classic Mobile Stand, MS3 Miscellaneous items Part number Description 104894 Pro6000 Rechargeable Battery 718584 Tether for PRO 6000 with 9 ft Cord 7000-APM Connex Spot Accessory Power Mgt Stand 7000-MS3 Connex Spot Classic Mobile Stand MS3 BATT99 Lithium-ion battery 9 Cell — Extended Life 7000-100S Ca
150 Connex® Spot Monitor Appendices Part number Description PWCD-P Line cord P, Thailand PWCD-Z Line cord Z, Brazil 6000-NC Nurse call cable 6000-916 Honeywell 1900 2D Scanner 6000-916HS Jadak 2D Scanner 4500-925 USB cable for wired connectivity 7000-BOX Connex Spot Packaging (Empty Box Set) 660-0321-00 Patch cable, 50' 660-0320-00 Patch cable, 100' 660-0138-00 Patch cable, 5' 6000-50 VSM 6000 USB Configuration Memory Stick 7000-PS Connex Spot 35 Watt Power Supply 4600-90E BP A
Directions for use Appendices Part number Description S4-CSM-5 CSM, Warranty Extension, 5 years 151 Literature/Documentation Part number Description 7000-DFU-CD Connex Spot CD Kit (Directions for use, Quick reference cards, Startup guide, Service manual) Applied parts FlexiPort cuffs Part number Model Description Neo-1-1 Neo 1 with new fitting Neo-2-1 Neo 2 with new fitting Neo-3-1 Neo 3 with new fitting Neo-4-1 Neo 4 with new fitting Neo-5-1 Neo 5 with new fitting Reuse-06 Reusable
152 Connex® Spot Monitor Appendices Part number Model Description Soft-07 Disposable CUFF, Welch Allyn, INFANT Soft-08 Disposable CUFF, Welch Allyn, SMALL CHILD Soft-09 Disposable CUFF, Welch Allyn, CHILD Soft-10 Disposable CUFF, Welch Allyn, SMALL ADULT Soft-11 Disposable CUFF, Welch Allyn, ADULT Soft-11L Disposable CUFF, Welch Allyn, ADULT LONG Soft-12 Disposable CUFF, Welch Allyn, LG ADULT Soft-12L Disposable CUFF, Welch Allyn, LG ADULT LONG Soft-13 Disposable CUFF, Welch
Directions for use Appendices 153 Part number Model Description LNCS-Inf-3 LNCS Disposable adhesive finger sensor - Infant (20 per case) Inf-Wrap-RP LNCS Replacement wrap for infant adhesives (100 per case) YI-AD LNCS Multisite adhesive wrap adult/pediatric/neonatal for YI sensor (100 per case) YI-FM LNCS Multisite foam wrap adult/pediatric/neonatal for YI sensor (12 per case) Nellcor pulse oximetry Part number Model Description DS-100A OxiMax Durasensor adult oxygen transducer D-YS
154 Connex® Spot Monitor Appendices Part number Description 0739-000 8001J NONIN NEONATAL FLEX SENSOR WITH 25 WRAPS 4777-000 8008JFW NONIN NEONATE REPLACEMENT WRAPS 25/PACK 7426-001 6000CA NONIN ADULT CLOTH DISPOSABLE 24/BX 7426-002 6000CP NONIN PEDIATRIC CLOTH DISPOSABLE 24/BX 7426-003 6000CI NONIN INFANT CLOTH DISPOSABLE 24/BX 7426-004 6000CN NONIN NEONATE CLOTH DISPOSABLE 24/BOX Braun thermometry Part number Description 06000-005 Disposable probe covers (5,000 covers, packaged 200/box
Directions for use Appendices 155 Warranty Welch Allyn warrants the product to be free of defects in material and workmanship and to perform in accordance with manufacturer's specifications for the period of two years from the date of purchase from Welch Allyn or its authorized distributors or agents. The warranty period shall start on the date of purchase.
