Related Manuals for GE MAC 800
Summary of Contents for GE MAC 800
- Page 1 GE Healthcare MAC™ 800 Resting ECG Analysis System Software Version 1 Operator's Manual 2031504-182 Revision F...
- Page 2 Archivist, CardioSoft, CASE, Hookup Advisor, MAC, Mactrode, Multi-Link, MUSESilverTRACE, and 12SL are trademarks owned by GE Medical Systems Information Technologies, a division of General Electric Company going to market as GE Healthcare. All other marks are not owned by GE and are instead owned by their respective owners.
- Page 3 Contents Introduction Manual Information ........... 1-2 Purpose .
- Page 4 Using the MAC 800 Keyboard........
- Page 5 Recording ECGs of Pacemaker Patients .......5-13 Recording ECGs during Defibrillation ........5-14 Arrhythmia Mode Recording Introduction .
- Page 6 Replacing the Battery ..........10-10 Conditioning the MAC 800 Battery Pack ......10-11 Supplies and accessories .
- Page 7 Equipment Problems ..........A-2 System Will Not Power Up .
- Page 8 MAC™ 800 Resting ECG Analysis System 2031504-182F...
- Page 9 Introduction 2031504-182F MAC™ 800 Resting ECG Analysis System...
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Page 10: Manual Information
Introduction Manual Information Purpose This manual describes the safe and effective operation of the MAC™ 800 Resting ECG Analysis System. Intended Audience This manual is written for clinical professionals who use, maintain, and/ or troubleshoot the MAC™ 800 Resting ECG Analysis System. Clinical professionals are expected to have a working knowledge of appropriate medical procedures, practices, and terminology used in the treatment of patients. -
Page 11: Product References
Indicates you must press the “Enter” or “Return” key on the keyboard. Do not type “enter”. Product References The name of the product described in this manual is MAC 800 ECG Analysis System. It will be referred to as “the system” or “the device” throughout this document. - Page 12 NOTE provides application tips or other useful information to assure that you get the most from your equipment. Applicable Messages The following safety information applies to the MAC 800 ECG Analysis System. WARNING ACCIDENTAL SPILLS — If liquids have entered a device, take it out of service and have it checked by a service technician before it is used again.
- Page 13 Patient signal inputs labeled with the CF symbol with paddles are protected against damage resulting from defibrillation voltages. To ensure proper defibrillator protection, use only GE-recommended cables and leadwires. Proper placement of defibrillator paddles in relation to the electrodes is required to ensure successful defibrillation. WARNING ELECTRODES —...
- Page 14 Introduction WARNING OPERATOR — Medical technical equipment such as this system must only be used by qualified and trained personnel. WARNING SHOCK HAZARD — Improper use of this device presents a shock hazard. Strictly observe the following warnings. Failure to do so may endanger the lives of the patient, the user, and bystanders.
- Page 15 Introduction WARNING BURN PROTECTION — To ensure defibrillator protection and protection against high-frequency burns, use only GE-recommended cables and leadwires. Otherwise, serious injury could result. WARNING HIGH-FREQUENCY PRECAUTIONS — Do not use the device with high-frequency surgical units. CAUTION ACCESSORIES (SUPPLIES) — To ensure patient safety, use only parts and accessories manufactured or recommended by GE.
- Page 16 If you have questions concerning disposal of the product, please contact GE or its representatives. CAUTION EQUIPMENT DAMAGE — Devices intended for emergency application must not be exposed to low temperatures during storage and transport to avoid moisture condensation at the application site.
- Page 17 Introduction CAUTION OPERATOR — Medical technical equipment such as this electrocardiograph system must only be used by persons who have received adequate training in the use of such equipment and who are capable of applying it properly. CAUTION POWER REQUIREMENTS — Before connecting the device to the power line, check that the voltage and frequency ratings of the power line are the same as those indicated on the unit's label.
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Page 18: Legal Notice
The parts of the product described in this operator’s manual, including all accessories, that come in contact with the patient during the intended use, fulfill the biocompatibility requirements of the applicable standards. If you have questions in this matter, please contact GE or its representatives. Legal Notice Our equipment contains several fields which can be filled in before performing an ECG. -
Page 19: Responsibility Of The Manufacturer
Responsibility of the Manufacturer GE is responsible for the effects of safety, reliability, and performance only if: Assembly operations, extensions, readjustments, modifications, or ... -
Page 20: Modulating Effects In Digital Systems
If the installation of this equipment, in the USA, will use 240 V rather than 120 V, the source must be a center-tapped, 240 V, single-phase circuit. Contact GE for information before connecting any devices to this equipment not recommended in this manual. Parts and Accessories To ensure patient safety, use only parts and accessories manufactured or recommended by GE.