instructions about the different therapies, see each respective therapy chapter. . Information . . . . . . . . . . . . . . . . . . Foreign objects on the scales can significantly alter, Leakages from the fluid bags can significantly alter fluid balance. . Rx Only. . . It. . . . . . . . . The labelling with a crossed-over waste bin indicates that the batteries shall not be, discarded in normal waste (see figure 1:1). . . . . that delivers the following: • from 100 (–10%) Vac to 240 (+10%) Vac; from 45 Hz to 65 Hz. Their use can impede. It also indicates that the notified body British Standards, Institution (BSI, No. . . . . . . . . . set and solution bag Instructions for Use before operating this device. . . . . . . . . . . . . Figure 2:5 on page 2:12 shows miscellaneous components. . . In this manual, Operator designates appropriately trained and qualified clinical staff, who is in charge of the Prismaflex control unit. . . . Instructions for Use of Prismaflex® Disposable Sets . Manufacturer. Prismaflex- Unidad de comunicación • Instrucciones paso a pasoque el operador sigue para configurar, administrar y finalizar los tratamientos. . . . . The Prismaflex control unit may not be able to detect all situations that can. . The PRISMAFLEX system is intended for: Continuous therapies – CVVHDF, CVVHD, CVVH, SCUF Plasma therapies – TPE. as its package and sterilization caps are removed. . . . Operate the Prismaflex control unit in accordance with this manual, the, Instructions for Use of the Prismaflex disposable set and solutions, and the, online instructions. . operator works within one meter from the front of the Prismaflex control unit. . . . . . . . . 0086) has approved the Quality Management System. . . . . . Variations in room temperature of ±3 °C (5.4 °F) or more can cause the scales, Before moving the Prismaflex control unit, check that the brake is released and. . Page 24. . . . . . . the detection of return disconnections, potentially resulting in severe blood loss. . . . . . . . . . . . connected to the Prismaflex control unit. . . . . . . . . . . . . . . . . . Additional multiple portable socket-outlets must not, Use only the Prismaflex hospital grade power cord to connect the. . . . . . . Check out our extensive catalog of New & Used Gambro AK95 Hemodialysis ... V2500 Manual Atari Cx 5200 Service Manual User Guide 2003 Chevy Trailblazer Manual Online Page 6/10. . . . . . . . . . . Blood or fluid leakage from a pod diaphragm or wetting of the fluid barrier, at the distal end of the monitor line will impair pressure monitoring in the, Prismaflex system and requires immediate troubleshooting. . . . . . . . . therefore be periodically verified by weighing the patient. . . . . . . . . . . . . . . . . . . . . 2:3. . Batteries found in Prismaflex control unit. . . . . The PRISMAFLEX TPE 2000 Set is indicated for use only with the PRISMAFLEX Control Unit, after having selected TPE therapy (therapeutic plasma exchange). The Prismaflex system consists of the Prismaflex control unit, a Prismaflex disposable, set, disposable solutions and optional accessories. In this manual, Responsible Organization means a function or a person who can identify, analyze, and control potential risks that could occur, for example, when connecting the, Prismaflex control unit to other equipment or when making changes to the equipment. . . . . . . . . . . . . Discarded electromedical equipment must not be disposed together with municipal waste, but must be collected separately in order to guarantee ecologically correct disposal to. . . . . Para obtener más información sobre los dispositivos mencionados aquí, consulte el Manual del Operador correspondiente. . . . This may require the use of, a new bag of priming solution and a new (empty) collection bag. If the equipment is used in accordance with this manual. Emissions and Immunity” on page 13:11 in this manual. . Certain components within this equipment are sensitive to electrostatic discharge. . . . . . . . The, CE conformity mark is only valid for the Prismaflex control unit. Rx Only. . . . On the disposable set the symbol is a relief. For the devices mentioned herein, please refer to the appropriate Operator's Manual. General Information . . . . . . . . . . . . . . . During the setup procedure, the operator selects the therapy desired. . . Calibration weights are to be removed before tilting the Prismaflex control. . . . . . . . The content of this page and media is intended for the Healthcare Professionals only and meant to guide on the safe and proper use of PrisMax control unit. . . . . . . . . . Before first use. . . . . . . . The use of incorrect solution/fluid can result in, The Prismaflex system is unable to detect all situations in which a fluid bag has, been attached to the wrong line or has been hung on an incorrect scale. . . . . . If Service mode. . If the electrical installation for powering the equipment complies with all applicable. . . . . . . There are no known contraindications to Continuous Renal Replacement Therapies. . . . . www.multiorgansupport.ch. . . . . . . . . . . . embolism. . Use aseptic technique when handling the blood and fluid lines in the disposable, Do not use the Prismaflex disposable set if the package is damaged, if the. . . . . . . . . . . . . . . Before connecting the blood return line to the patient, make sure the blood line. . . therapeutic or pharmacological action for the patient. . . Solutions . . . . . If found, refer to the manual. . For technical assistance, contact your local Gambro representative. Be, sure that the test is conducted using a container of water to substitute for the, The Prismaflex control unit weighs approximately 78 kg (172 lb). . . . . . than disposed together with other municipal waste; – the equipment was placed on the market after 13 August 2005. . . . for use of the set with the Prismaflex system. Upper and lower limits are expressed with, Humidity limitation. . . . . . . . . . . . . . . . . . . operator is obliged to periodically monitor the patient in person. . . . . . . Contraindications . . Prismaflex® Control Unit . . . . Specific therapy information is, CRRT in chapter 5: “Continuous Renal Replacement Therapies (CRRT)”, TPE in chapter 6: “Therapeutic Plasma Exchange (TPE)”, Anticoagulation in chapter 8: “Anticoagulation Methods”, Detailed operating instructions are incorporated in the software of the Prismaflex control, unit. . . . . . Prismatherm II extension line . . . . . . . . Calcium Infusion Line . . . . Depending on the, therapy in use, these processes can include fluid removal and/or solute clearance. . . . . . . . . . . . . . . . . . . treatment according to therapy configuration. . . . two people to lift it out of the shipping carton. . . . . . . . . Siamo lieti di presentare i miglioramenti all’interfaccia utente e alla versione 5.XX del software. . disposables. Certification Marks . Box 10101, Magistratsvägen 16, SE-220 10 Lund, Sweden, Tel: +46-46-16 90 00, Fax: +46-46-16 96 96. El sistema PRISMAFLEX está diseñado para: Terapias continuas, como CVVHDF, CVVHD, CVVH, SCUF Terapias de plasma, como la RPT. . . . . . . Since Gambro has no control over service work which is not performed by authorized, service technicians, Gambro will in no way be responsible or liable for any damages. ensure that the installation test has been successfully performed. . . Symbols . . Gambro does not accept any responsibility or liability for use of accessories, or disposables other than those specified in this manual or if any specified accessory, or disposable is not used in accordance with this manual, online instructions and the. . Device requires an alternating supply current. . . . . . . . . . . . . . . . . . . . . O sistema PRISMAFLEX só deve ser usado em pacientes com peso corporal superior a 20 kg (44 lb). . . . . . Disposal of Packaging Material . . shape in the plastic cover indicating the effluent pump. . . . . . . Gambro Prismaflex Operator Manual - www.wsntech.net Gambro AK95 Hemodialysis Machine for Sale. . . . for some minutes before taking a blood sample to obtain stabilized conditions. It is backed by Baxter’s broad acute product portfolio and commitment to the needs of ICU patients and practitioners. . . O sistema PRISMAFLEX destina-se a: Terapias contínuas – CVVHDF, CVVHD, CVVH, SCUF Terapias plasmáticas – TPT. . . . . . . . . . . . (See “Prismaflex® Disposable Sets”, The CSA (C-US) mark indicates that the Prismaflex control unit conforms to the, requirements related to safety of medical devices for the US and Canada. . . . The, CRRT – Continuous Renal Replacement Therapies, CVVH – Continuous Veno-venous Hemofiltration, CVVHD – Continuous Veno-venous Hemodialysis, CVVHDF – Continuous Veno-venous Hemodiafiltration, CRRT septeX – Continuous Renal Replacement Therapies with high cut-off, CVVHD+post – Continuous Veno-venous Hemodialysis + post infusion, CRRT MARS®– Continuous Renal Replacement Theapies supporting Molecular, Note: All therapies beside CRRT require a service configuration. . . . . . . . Patient Data Management Systems and Remote Alarms, If a Patient Data Management System (PDMS) is to be used with the, Prismaflex system, the Responsible Organization is obliged to verify, compatibility between the two systems. . . Per una guida completa, consultare il Manuale Operatore del sistema Prismaflex®. . . service manual which contains all necessary circuit diagrams, calibration instructions, and service information to enable authorized service technicians to repair those parts of this equipment which Gambro considers to be repairable. . . . . . . . . . . . Pull out scale completely before hanging bag. . . Do not connect additional devices between the, Collecting blood samples from improper sample sites in the set can lead to, incorrect blood chemistry results. . . . . . . . . Use aseptic technique whenever inserting needles into sample sites. . . . The Prismaflex system is intended for: Continuous therapies – CVVHDF, CVVHD, CVVH, SCUF Plasma therapies – TPE. . . 2009;28(2):135-43. . . . Consult physician's prescription. . . . . . . . . . . . . . . . . . . aromatic and aliphatic solvents or ketonic solvents. . Solo con prescripción médica. . . . . . . 8.1 . . Connected cables must have a Kitagawa RFC-10. . . . prevent dispersion of potential pollutants into the environment. . . . . . . There are no known contraindications to Therapeutic Plasma Exchange. . . . Lock brakes on the wheels to limit movement of the control unit that might pull. . . . . . . . . . . . . . . . . . . . The use of a PDMS not compatible, with the Prismaflex system can result in presentation of erroneous data. Selectable by the user in steps of 1.0 °C Operating mode continuous duty Excessive temperature alarm monitored by two independent sensors 43.6°C (± 0.5°C) Low Temperature Alarm Tset -3°C for >10 minutes ... (for use with low flow PRISMAFLEX System M60 Hemofilter Set) . . Responsibility and Disclaimer . . . . . . Honoré PM, Joannes-Boyau O, Collin V, Boer W, Jennes S. Continuous hemofiltration in 2009: what is new for clinicians regarding pathophysiology, preferred technique and recommended dose? . . . . . . . . . Prismaflex system, see chapter 2: “Description of the Prismaflex® System” on page 2:1. . . . . Control Unit . . . . The Prismaflex control unit operates from an electrical power source. . . . . The use of operating or maintenance procedures other, than those published by the manufacturer, or the use of accessory devices not. . . . . . . . . . . . Operator’s Manual . . . . This symbol is applied on the stand if the Prismaflex calibration weight kit is stored, inside. . . . . . . Atmospheric pressure limitation. Upper and lower limits are expressed with numeric values, Circle sign; placed as colored symbol on effluent scale and in the graphical user, interface in screens related to effluent. prismaflex CRRT machine version 6.xx user manual . . Nearby high-voltage conductors could be hazardous if contacted. . may contain toxic substances which, if released into the. . . . . technician. . The use of additional devices, such as three-way valves, stopcocks, or, extension lines, may impair return pressure monitoring. This symbol warns against an incline of the Prismaflex control unit of more than, Note: This warning label must be applied on the warmer holder before use. . . . . . . . . The Prismaflex system has been tested and validated for use with these accessories and. . . . should be disposed of according to local regulations. . . . The THERAPY INFO softkey provides information on the therapy possibilities such as SCUF, CVVH, CVVHD, or CVVHDF. . . Pay particular attention to the extracorporeal blood volume. . . . . The overall fluid balance must. Installation, Service and Transport . . . . Disposal . . Devices connected to the RS232 serial communication port or the Ethernet port, must comply with IEC 60950. . . . . . . . . . . Disposal of Waste Batteries and Accumulators, According to Directive 2006/66/EC and RAEE Directive concerning batteries the, manufacturer shall provide instructions how to replace/remove batteries in a safely and, environmentally friendly manner. . . . . . . . . . . . . . . . . . Please refer to the Operators Manual for further information. . . . . Cautions . . . View online or free download from eBooks-go.com The Prismaflex System - Gambro The Prismaflex System. . . Nxstage crrt user manual - free download - Nxstage crrt user manual pdf. . . When a set is loaded, the bar code reader automatically scans the Misinterpretation of ECG readings due to artefacts may, Carefully observe the Prismaflex treatment system, including the disposable, Monitor patient blood chemistry to ensure electrolyte balance and, Monitor patient temperature to avoid hypo- or hyperthermia. . Bookmark File PDF Gambro Dialysis Machine Manual ARTIS GAMBRO PDF Operator’s Manual service code revision rev. Chemicals other than those recommended in this manual for cleaning and, disinfection could damage the Prismaflex control unit and Prismaflex disposable, sets. . . Prismaflex® Graphical User Interface 3. . . . . . Disposable Accessories . . . . Manual Usuario Phoenix Gambro (eng) [x4e65eyj83n3] in boluses (See Prismaflex Operator Manual for specification). For detailed instructions about the different anticoagulation methods, see chapter 8: During the setup procedure, the operator selects the desired anticoagulation method. . . . . When the reminder time expires the notification message will be displayed. . . . . . . . . . . . . . Air may enter into the extracorporeal circuit at connection points downstream of, the air detector if pressures are negative. . . . Do not resterilize. . Attention, consult accompanying documents. . . . . . package insert for environmental requirements, including storage conditions. . . . . . . . . . . . . . . . For contraindications that may apply to the disposable set selected for the therapy, refer to. . If leakage cannot be stopped by tightening the connections, replace the set. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . Ensure that the patient's blood return, connection is firmly secured. . . . . . . . . . . Fluid balance deviations, even if within the specified Prismaflex control unit. a relief shape in the plastic cover indicating the replacement pump. . . . . Baxter - Gambro Prismaflex System Flexibility that meets the strict demands of multiple blood purification therapies. Prismaflex control unit to the facility’s electrical outlet. Intended Use . . . . . . Blood Warmers . This term refers to Gambro trained and certified service technicians. . . . . . . . . . . . . Gambro will provide, on request, a service manual which contains. . . . Contact your local. . . General Warnings and Cautions . Procedures using the Prismaflex system must be performed under the, Service and repairs are only allowed to be performed by an authorized service, Ensure that scales and pressure sensors of the Prismaflex control unit are, accurately calibrated. . . Rear Panel Components . . . . . . . . . . . . . . . . Leakage can cause blood loss or air embolism. . . . . harmful substances (Hg = Mercury, Pb = Lead, Cd = Cadmium). . . . . . . . . . . . Do not, connect additional devices between the return line and the blood access, device. . Do not connect a patient to the Prismaflex system during the installation test. . . . After pumps have (re)started, wait. . . . . Prismaflex user manual - Free ebook download as PDF File (.pdf), Text File (.txt) or read book online for free. . . . . . . . Pay careful attention to the possible medical hazards associated with, Blood return from a blood primed extracorporeal circuit can result in.
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