Cardiocap™/5 a Technical Reference Manual ‘Oo Document Number 6050-0006-345 February 2003NOTICE Intended use The Datex Ohmeda Cardiocap/'S and accessories are indicated for indoor manitoring of hemodynamic (EC, impedance respiration, NIBP, temperature, Sp02, and invasive pressure). respiratory (C02, 02, N20, respiration rate, anesthetic agent, and agent identification), ventilatory (airway pressure, volume, and flow), and relaxation status (NMD of ll hospital pationts With the N-OSAT option, monitoringaf arteriat oxygen saturation includes monitoring hospital patents during conditions of clinical patient mation. Cardioeap/S is indicate for patients weighing 5 kg (11 i.) or more, Impedance respiration measurement is indicated for patients ages 3 years and older. ‘The monitoris indicated for use by qualified medical personnel only. CAUTION: US Federal lew restricts this device to sale by or on the order of a licensed medical practitioner. Outside the USA, check local laws for any restriction that may apply. Classifications ee 60601-2: = Typeot protection agains electric shock: Class equipment | Degree of protection against electric shock (indicated by a symbol an the panel beside each connector Type BF applied part or ype CF applied pan. The equipment isnot suitable for use in the presence ofa flammable anesthetic mixture wit a or with oxygen or nitrous oxide * Made of operation: Continuous. IEC 60529 (degree of protection against harmful ingress of water): PX1 EU Medical Device Directive: Ib Responsibility of the manufacturer atex Ohmeda Division, Instrumentarium Comp. is responsible for the safety, reabilty and performance of the equipment only if ‘+ Assembly, operation, extensions, eadustments, mocifications, service, and repairs are camied out by personnel authorized by Datex Ohmeda ‘© Electnical installation complies with appropriate requirements, ‘© The equipment is used in accordance with the Cardiocap/' User's Guide and serviced and maintained in ‘accordance with the Cardiocap/'5 Technical Reference Manual. Datex-Ohmeda assumes no esponsibility forthe use or reliability ofits software on equipment tat isnot ‘umished by Dates-Ohmeda. Trademarks Datex®, Ohmedat®, and other trademarks (Cardiocap/9, AS/3, CS/3. /', 6/5 light, Delite, Ped-Ite, Dtend, Dfend+, MemCard, ComWheel, EarSat, flexSat, OxyTip, Patient Op, and Patient Spirometry) are the property of nstrumentarium Corp ois subsidiaries Nello is a registewed trademark of Mallinckeodt Ine All other product and company names are the property af their respective owners, © 2003 Datex-Ohmeda, tne. All rights reserved,Cardiocap/5 Technical Reference Manual “Part |- General Service Guide Overview ES Monitor Structure Safety Precautions Product Specifications Installation and Functional Check 2 Installation Interfacing Functional Check Functional Check Form: Planned Maintenance 3 Planned Maintenance Instructions Planned Maintenance Form Troubleshooting 4 Messages Troubleshooting Charts Part Il - Product Service Guide Frames and Software 5 Hemodynamic Frame (F-MX) Hemodynamic with Airway Gases Frame (F-MXG) Anesthesia and Critical Care Software Measurement Parameters 6 Parameter Unit (NESTPR) Invasive Pressures and Second Temperature Option (N-XP) Nelicor Pulse Oximetry Option (N-XNSAT) Datex-Ohmeda Enhanced Pulse Oximetry Option (N-XOSAT) Airway Gas Options (N-XC, N-XCO, N-XCAiO) Patient Spirometry Option (N-XV) NeuroMuscular Transmission Option (N-XNM1) Service Procedures 7 Repair and Replacement Checks, Adjustments, and Calibration ServiceMenus 8 SpareParts 9