WARNINGELECTRIC SHOCK HAZARD/SYSTEM MALFUNCTIONLiquids inside a device can cause electric shock or system malfunction.Do not allow liquids to enter the device. If liquids enter the device, turn it off and informyour service technician. Do not use the device until it is checked by a service technician.WARNINGELECTRIC SHOCKImproper connection of this equipment may cause electric shock.To avoid risk of electric shock, this equipment must only be connected to a supply mainswith protective earth.NOTEFollow the instructions provided. Do not position equipment in a way that makes it difficult todisconnect the device when using an appliance coupler, mains plug, or other separable plugas a means of isolation.1.5.3 Classification of Medical DeviceThe device is classified as follows, according to IEC 60601-1:Category ClassificationType of protection against electrical shock Class I internally powered equipmentDegree of protection against electrical shock Type CF defibrillation-proof applied partDegree of protection against solids The IP code for this device is IP20.Protected against solid foreign objects with a diameter of 12.5mm and greater.The object probe, a sphere 12.5 mm diameter, shall not fullypenetrate. The jointed test finger 12 mm diameter, 80 mmlength, shall have adequate clearance from hazardous parts.Degree of protection against harmful ingress of liquids(IP20)The IP code for this device is IP20.Non-protectedThis device is ordinary equipment (enclosed equipment with-out protection against ingress of liquids).Degree of safety of application in the presence offlammable anesthetic mixture with air or with oxygenor with nitrous oxideEquipment is not suitable for use in the presence of a flamma-ble anesthetic mixture with air or with oxygen or with nitrousoxide.Method(s) of sterilization or disinfection recommen-ded by the manufacturerNot applicableMode of operation Continuous operationOperator Manual 1.5 Regulatory and Safety Information2053535-002 Revision T MAC 2000 ECG Analysis System 15/198