The left keypad is engraved with indicators for embossed bell and embossed plus-minus. The right keypad is engraved with labels for emboss. The plastic kit is comprised of door battery, battery label, help card tray, cover for help card tray, battery pad support, cable tie, rear printer housing, front display case, grommet extruded, gray round rubber feet, adhesive.
The kit part is comprised of user interface board PWA board, anti-static bag, anti-static label, carton box with foam and BOM label. Please contact Service Shop Team to learn how to gain access to this content. United States. Please Enter Valid Text. Your cart has been saved and will be available when you login next time. You have a cart already in session. What action do you want to perform? Continue Checkout. I Agree. View Cart Continue Shopping.
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Please enter appropriate Account ID. Patient Applied Parts. Packaging Material. Equipment Description. Product Configurations. Basic Components. Front Panel. Product Compliance. Theory of Operation. Overall Principles of Operation. Systolic Search. Functional Description. Main Board PWA. SpO2 PWA. Optical Switch. Right-Side Panel. Rear Panel. Powering the Monitor. Power Sources. Battery Charging. Battery Alarms. E13 Battery Low.
Unpacking and Preparation for Installation. Configuring Your V Monitor. Operating Modes. Clinical Mode. Configuration Mode. Advanced Configuration Mode. Service Mode. Host Communications Connector. DB15 Connector Pin Assignments. Connection Details.
Preventative Maintenance. Integrity of Hoses and Cuffs. Visual Inspection. Cleaning the Monitor. Temperature Devices. SpO2 Sensors. Long-Term Storage. Battery Care. Replacing the Battery. Parameter Level Functional Testing. Parameter Test Procedures. Test Results Form. Alarm Code Interpretation.
System Failures. Alarm Conditions and Error Codes. Error Log. Error Codes. Ordering Parts. Service Parts. Compatible Parts. FRU List. FRU Photos. Monitor Disassembly Procedure. Rear Case. SpO2 Board. Front Bezel. Main Board. Display Board. Ohmeda SpO2. Nellcor SpO2. Masimo SpO2. Default Settings. NIBP Accuracy. B-3 Clinical vs. Simulator Readings. B-4 Why Use Simulators? B-5 Summary. Recommended Separation Distances. Compliant Cables and Accessories.
Each page of this manual has a revision letter located at the bottom of the page. This letter identifies the revision level of the entire manual. This may be important if you have different manuals and you do not know which is the most current. For the initial release, all pages have the revision letter A.
For the second update, all pages receive the revision letter B. The latest letter of the alphabet added to the table below corresponds to the most current revision. B Updated CE marking information. This manual supplies technical information for service representatives and technical personnel so they can maintain the equipment to the assembly level.
Use it as a guide for maintenance and electrical repairs considered field repairable. Where necessary the manual identifies additional sources of relevant information and technical assistance. See the operator's manual for the instructions necessary to operate the equipment safely in accordance with its function and intended use.
A paper copy of this manual will be provided upon request. Contact your local GE representative and request the part number on the first page of the manual. The information presented in this section is important for the safety of both the patient and operator. This chapter describes how the terms Danger, Warning, Caution, Important, and Note are used throughout the manual. In addition, standard equipment symbols are defined.
GE is responsible for the effects on safety, reliability, and performance only if:. This device is intended for use under the direct supervision of a licensed health care practitioner. This device is not intended for home use. Federal law restricts this device to be sold by or on the order of a physician. Contact GE for information before connecting any devices to the equipment that are not recommended in this manual.
Periodically, and whenever the integrity of the device is in doubt, test all functions. Consideration relating to the choice shall include:. If the installation of the equipment, in the USA, will use V rather than V, the source must be a center-tapped, V, single-phase circuit.
Extreme care has been taken to use fictitious names and related information in the examples and illustrations provided herein. Any similarity of this data to persons either living or dead and to either current or previously existing medical institutions should be regarded as coincidental. The terms danger, warning, and caution are used throughout this manual to point out hazards and to designate a degree or level or seriousness. Familiarize yourself with their definitions and significance.
Hazard is defined as a source of potential injury to a person. WARNING indicates a potential hazard or unsafe practice which, if not avoided, could result in death or serious injury. NOTE provides application tips or other useful information to assure that you get the most from your equipment. There have been reports of sensors causing patient burns when operating in an MRI environment. The use of approved accessories will provide protection from burns during HF surgery.
To help prevent unintended current return paths with the use of high frequency HF surgical equipment, ensure that the HF surgical neutral electrode is properly connected. To avoid personal injury, do not perform any servicing unless qualified to do so. These Monitors should not be used on patients who are connected to cardiopulmonary bypass machines.
If powering the Monitor from an external power adapter or converter, use only GE Medical Systems Information Technologies -approved power adapters and converters. The Monitor does not include any user-replaceable fuses. Refer servicing to qualified service personnel. To reduce the risk of electric shock, do not remove the cover or the back. Refer servicing to a qualified service person.
Use of portable phones or other radio frequency RF emitting equipment near the system may cause unexpected or adverse operation. The equipment or system should not be used adjacent to, or stacked with, other equipment. If adjacent or stacked use is necessary, the equipment or system should be tested to verify normal operation in the configuration in which it is being used. The use of accessories, transducers and cables other than those specified may result in increased emissions or decreased immunity performance of the equipment or system.
Do not use replacement batteries other than the type supplied with the Monitor. The V Monitor is designed to conform to Electromagnetic Compatibility EMC standard IEC and will operate accurately in conjunction with other medical equipment which also meets this requirement. To avoid interference problems affecting the Monitor, do not use the Monitor in the presence of equipment which does not conform to these specifications. Place the V Monitor on a rigid, secure surface.
Monitor must only be used with mounting hardware, poles, and stands recommended by GE Medical Systems Information Technologies. Verify calibration of NIBP parameter temperature and pulse oximeter do not require calibration.
Ensure that the display is functioning properly before operating the V Monitor. Do not immerse the Monitor in water. If the Monitor is splashed with water or becomes wet, wipe it immediately with a dry cloth. The V Monitor, when used with GE Medical Systems Information Technologies-approved applied parts and accessories, is protected against defibrillator damage. NOTE: The electromagnetic compatibility profile of the V Monitor may change if accessories other than those specified for use with the V Monitor are used.
NOTE: The model of the monitor determines which symbols appear on it. Manufacturer: This symbol is accompanied by the name and the address of the manufacturer. Manufacturing Date: This symbol is accompanied by the date of the manufacturing. European authorized representative. Packaging label depicting the transportation and storage atmospheric pressure range of to hPa. Please contact an authorized representative of the manufacturer for information concerning the decommissioning of your equipment.
Vertically falling drops shall have no harmful effects to the Monitor. Any unauthorized attempt to repair equipment under warranty voids that warranty. Failure on the part of the responsible individual, hospital or institution using this equipment to implement a satisfactory maintenance schedule may cause undue equipment failure and possible health hazards.
Regular maintenance, irrespective of usage, is essential to ensure that the equipment will always be functional when required. This manual is intended for service representatives and technical personnel who maintain, troubleshoot, or repair this equipment.
The V Monitor is intended to monitor one patient at a time in a clinical setting. Federal law U. To ensure patient safety, use only parts and accessories manufactured or recommended by GE Medical Systems Information Technologies. Parts and accessories used shall meet the requirements of EN Disposable devices are intended for single use only. They should not be reused. Periodically, and whenever the integrity of the monitor is in doubt, test all functions.
The warranty for this product is enclosed with the product in the shipper carton. All repairs on products under warranty must be performed or approved by Product Service personnel. Unauthorized repairs will void the warranty. Only qualified electronics service personnel should repair products not covered by warranty.
If the product fails to function properly, or if assistance, service or spare parts are required, contact Customer Support. Before contacting Customer Support, it is helpful to attempt to duplicate the problem and to check all accessories to ensure that they are not the cause of the problem. If you are unable to resolve the problem after checking these items, contact GE Medical Systems Information Technologies.
Prior to calling, please be prepared to provide:. If your product requires warranty, extended warranty or non-warranty repair service, call Customer Support and a representative will assist you.
Replacement batteries are available from GE. NOTE The model of the monitor determines which symbols appear on it. Page 19 Manufacturer: This symbol is accompanied by the name and the address of the manufacturer.
Manufacturing Date: This symbol is accompanied by the date of the manufacturing. Page 20 WEEE : This symbol indicates that the waste of electrical and electronic equipment must not be disposed as unsorted municipal waste and must be collected separately.
Page Related Manuals If you are unable to resolve the problem after checking these items, contact GE. Page Packing Instructions As you use the monitor, you will accumulate solid wastes that require proper disposal or recycling. These include batteries, patient applied parts, and packaging material.
Dispose of these materials according to local or national regulations. Page Batteries At the end of its service life, the product described in this manual, as well as its accessories, must be disposed of in compliance with the guidelines regulating the disposal of such products.
If you have questions concerning disposal of the product, please contact GE or its representatives. The contents of the pack vary according to model. Unpack the items carefully. If an accessory is missing or if an item is in a nonworking condition, contact GE Customer Service immediately.
Temperature probe holster: stores Alaris temperature probe. Page Right-Side Panel less than 45 minutes when solid; 5 minutes or less when flashing. Temperature window: indicates measured temperature. Page Rear Panel Printer door. Host communication port The host communication port is used to interface the CARESCAPE V vital signs monitor with other electronic devices a central nurse's station or remote alarm device , or with the Exergen scanner.
For further information, reference the Host Communication manual. Page Product Compliance GE sales representative for the latest information on connectivity solutions for your monitor. Pressure transducers PT1 and PT2 monitor pressure information. Page Dinamap Superstat Algorithm The figure shows a full determination sequence for an adult patient.
In Stat mode, some steps may require only one pulse. Page 34 The algorithm will inflate above the initial target pressure to obtain more data in the systolic region. The pressure is limited to the maximum allowed for the selected patient type. Page Dinamap Classic And Auscultatory Reference Algorithm At each step the microprocessor stores cuff pressure, the matched pulse amplitude, and the time between successive pulses. Page Reference Used To Determine Nibp Accuracy For neonatal mode, the reference is always the intra-arterial pressure monitoring method.
Page Temperature The Turbo Temp or Tri-Site temperature options support two different temperature measurement modes of operation: fast predictive or continuous monitor. Page Exergen Temperature The Power processor is powered at all times. The temperature processor controls the temperature parameter. The information is sent to the Main Board via the optically coupled electrically isolated serial connection. The primary processor receives the data and routes it to the UI board for display.
The data is also sent to the printer if specified. Page Printer Optical switch The optical switch indicates whether the Alaris temperature probe is inserted in the probe holder or not. The Main Board powers the switch. NOTE Use only the original cord, a power cord recommended by GE, or a regulatory-approved cord for the country of use. If the alarm is not acknowledged, the alarm is re-issued every 8 seconds.
To continue with other changes, press the Menu button. Page 51 Press the Menu button until n0d averaging time appears in the Pulse Rate window. Press the Menu button once. On the back of the scanner, loosen the single screw at the bottom and remove the cover.
Page Advanced Configuration Mode After a moment, this version information is cleared, and the monitor displays the first page of configuration mode which simply displays ACF in the Systolic display window indicating that the monitor is in advanced configuration mode. To save settings in service mode, advance to the last page page 6 , then press and hold the Menu button until the second of two tones sound. When a high-priority alarm condition is displayed on the monitor, the remote alarm signal becomes active within 0.
Contact your GE sales representative for further information. The sole responsibility rests with the individuals, hospitals, or institutions utilizing the device. WARNING Use of unapproved cleaning agents can cause case damage resulting in unintended fluid ingress and a potential for compromising electrical safety. Page Scanner Do not use bleach or other cleaning solutions on the sensor lens. Allow 2 hours for drying.
The user has the responsibility to validate any deviations from the recommended method of cleaning and disinfection. For additional information on infection control procedures, contact GE Technical Support. Page Cleaning The Exterior Surfaces Of The Alaris Temperature Devices If you question the effect your specific cleaning agent or disinfectant has on your instrument, contact your local GE Healthcare sales and service office or distributor. Do not use alcohol, ammonia, or ammonium chloride-based agents, as they could damage the plastic exterior of the probe.
Page Battery Care It is best to keep the battery charged as fully as practical and never store the monitor with the battery in a discharged condition. When the battery will no longer hold a charge, remove the battery and replace it with a GE-approved battery. Failure to use a GE-approved battery may cause the monitor to shut down.
When the battery is replaced, all user settings are lost and return to default values. Replacement batteries can be obtained from GE. Looking at the bottom of the monitor, remove the battery compartment cover by removing the four screws that secure the cover and help card tray. Page Exergen Temporal Scanner Battery Replacing the Exergen temporal scanner battery Disconnect the scanner cable from the monitor.
Page Fuses DC input, the main battery, and the remote alarm output. Fuses are not replaceable. Page Parameter Level Functional Testing Take an oral or axillary temperature reading on yourself i. Verify that a predictive temperature begins once the probe is removed from its holster.
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