fresenius kabi agilia service manual

By continuing to browse the site you are agreeing to our use of cookies. Please review our Privacy Policy for more details. All Rights Reserved. Sign in Forgot Password. My Bench Close Sign In Not A Member. Sign Up Join MedWrench OK name type Receive Summary Emails. This will also help other community members who face similar challenges. You are about to submit an abuse report for this post. By continuing to browse the site you are agreeing to our use of cookies. Please review our Privacy Policy for more details. All Rights Reserved. A collection of service manuals, tutorials and descriptions of medical equipment. Fresenius Injectomat MC Agilia. Fresenius prevention of accidental free flow.A password reset link will be sent to you by email. Injectomat Agilia Technical Manual Eng.Injectomat Agilia is fitted at the back with an infrared cell. Injectomat Agilia is equipped with an integrated system allowing it to be fixed onto a pole or a rail. Its integrated locking system allows three Agilia IV pumps to be stacked on top of one another to facilitate transportation. Operation diagram Supply Mode, battery management, battery life indication Introduction Precautions for use Fresenius Kabi recommend a complete reading of the Instructions For Use manual, in accordance with norm EN 60 601-1. ! Fresenius Kabi cannot, in any circumstances, be held responsible for any medical or other problem due to incorrect use of the device. Kindly consult the Instructions For Use manual for more details. Atmospheric pressure: 700hPa to 1060hPa. Operation safety As soon as it is in operation, the Injectomat Agilia syringe pump ensures continuous surveillance of its functions. Any internal fault or any procedural anomaly is immediately detected. Nevertheless, abnormal functioning of the device, without a defined cause, must always be brought to the attention of the qualified staff in your establishment or our Technical Service.

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Blood warmer see the Fluid Warmer section. Infusion pumps of Alaris, Imed and CardinalHealth might be identical as well as BME and CME. Support is not desired. Argus 708 Support is not desired. B. Braun Horizon Nxt Support is not desired. Graseby 500, 505 Support is not desired. Graseby 3100 Support is not desired. Graseby 3300 Support is not desired. Graseby 3400 Support is not desired. Grasby Omnifuse PCA Support is not desired. Grasby Omnifuse Syringe Pump Support is not desired. Grasby Omnifuse Support is not desired. Graseby MS16A,26 Support is not desired. Hospira Acclaim Support is not desired. Nutricia F-800 Support is not desired. Smiths Medical Cadd-Legacy PCA Support is not desired. Smiths Medical Cadd-Legacy Plus Support is not desired. Smiths Medical Cadd-Prizm PCS 2 Support is not desired. Smiths Medical Cadd-Prizm VIP Support is not desired. Stihler Astotherm AP-220-260. Sign in Forgot Password. My Bench Close Sign In Not A Member. Sign Up Join MedWrench OK name type Receive Summary Emails. Combines a friendly, lightweight pump packed with features and functionality that can adapt to the way you work and grow, and offers steadfast support to get you up and running. It’s a smart approach using proven technology that makes the transition today and transformation tomorrow. FORUMS View All (3) Ask a New Question 1 Reply -leroyman2 7 months ago 7 months ago Syringe calibration kit Hi all, hope you well. Just wanted to know where I can buy syringe calibration kits? I have tried contacting technical support and searched the service manual but have had no luck. Reply SERVICE COMPANIES View All Infusion Pump Companies BMES Contact Mountain States Biomedical Services Contact FDA Alerts View All Fresenius Kabi Recalls Volumat MC Agilia Infusion Pump and Vigilant. The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. This site uses cookies.

Important: If these maintenance procedures are not observed, the pump correct operation will be impaired. Quality control At the request of the health organisation, a quality check will be carried out every 12 months. A quality check (not included in the guarantee) consists of different inspection procedures as defined in the pump Technical Manual. Only a qualified technician may perform the quality check which must be performed using Fresenius Kabi software. For more information, kindly contact our Technical Service. Recycling of obsolete batteries and devices: Before disposal, remove battery from the device. Batteries and devices with this label must not be disposed of with the general waste. They must be collected separately and disposed of according to local regulations. For further information pertaining to waste processing regulation, contact your local Fresenius Kabi. Preventive maintenance Checks A quality control certificate is available at the end of this section. In order to ensure the smooth running of the checking procedure, recharge the battery for 16 hours beforehand. Keyboard description. Key Function ON switches on the pump. OFF switches it off when pressed for over three seconds. SILENCE ALARM STOP stops infusion. The selection keys scroll through the numbers and letters on the tenths, units and tens values and allow one to move to the next menu. OK validates your test selection or moves the cursor.It is advisable to clean and disinfect the device external surfaces regularly and especially before connecting a new patient and before any maintenance operation in order to protect patient and staff. Disconnect the device from its main supply before cleaning. Do not place in an AUTOCLAVE nor IMMERSE the device. Do not let liquids enter the device housing. If the device is placed in a high contamination risk unit, it is advisable to leave it in the room during disinfecting, after having disinfected it with amoist cloth.

The alarm for the most rapidly detected discrepancy is activated. Injectomat Agilia is equipped with an internal battery that ensures normal functioning during a mains power cut. In addition, a safety fuse protects the concerned mains area.Protection against leakage current: Defibrillation-proof type CF applied Protection against electric shocks: class II. Description and operation Physical description Flanges groove Plunger protection Cover Plunger disengagement control Angle bracket Plunger Base Syringe clamp Control panel Injectomat Agilia is made up of three main parts: a base, a cover and an angle bracket. The cover contains: a display board. The base contains: a CPU board a mechanical framework assembly a plunger unit. The angle bracket contains: a power supply board and a battery Fixing clamp system. Preventive maintenance Recommendations The device can only be checked, serviced or repaired by Fresenius Kabi or by a certified and approved maintenance service. Any abnormal functioning of the pump must be brought to the attention of your in house qualified technical personnel or our Technical Service. Should you need to return the pump to our Technical Service, it should be cleaned, disinfected and very carefully packaged, preferably in its original packaging, before being shipped. For all information concerning the repair and use of the pump, kindly contact our Technical Service or our Customer service. Fresenius Kabi is not liable for loss or damage to the pump during its transport to our Technical Service. Maintenance schedule Preventive maintenance In order to maintain the pump’s performances, a preventive maintenance inspection must be carried out every 3 years. This procedure, which includes battery replacement, should be carried out by a qualified technician. Any abnormal functioning or failure must be reported to the qualified technical staff in your organisation or to our Technical Service. In these instances, the pump should not be used.

Recalibrate the position sensor (Cal 3) with maintenance software. Flow rate or displacement control drift. The installed syringe doesn't correspond with the selected syringe. The position sensor calibration values have drifted. Replace or confirm the right syringe brand. Check the position sensor calibration values and recalibrate it if necessary. Change the position sensor. Occlusion alarm after the device has been turned on. Wrong calibration of the force sensor. Force sensor is out of order. Flexible circuit cut. Occlusion alarm during the infusion. The pressure limit selected is too low. Wrong calibration of the force sensor. Flexible circuit cut. Disengagement alarm after the device has been turned on or during the infusion. The disengagement micro-switch is defective. Carriage flexible circuit is cut. Unjustified alarm of plunger head position. Recalibrate and check the force sensor. Replace the force sensor. Replace the flexible circuit. Select a higher pressure limit. Recalibrate and check the force sensor. Replace the flexible circuit. Replace the micro-switch. Replace the flat ribbon cable. Check the anti-siphon system Check the good condition of the pusher internal mechanism. Replace the flat ribbon cable. Flexible circuit cut. Defective syringe holder potentiometer. Flat ribbon cable is defective. Check the syringe holder and replace the defective parts if necessary. Display defect: LED, screen. Check the good condition of the display board. Replace the LED or the control transistors. Check the connectors linking the CPU and display boards. Replace the display board. Device turns off when mains cord disconnection. The battery is unplugged or the battery cable is cut. The power supply LED doesn't lit. Battery is totally discharged. Power supply board is defective. Check the battery connection. Replace the battery. Replace the power supply board. Problem Cause Action Battery alarm while it has been completely charged.

Use a cloth soaked in DETERGENT-DISINFECTANT, previously diluted with water if required, to destroy micro organisms. Avoid abrasive scrubbing which could scratch the casing. Do not rinse or wipe the surfaces. Do not use: TRICHLOROETHYLENE-DICHLOROETHYLENE. AMMONIA. AMMONIUM CHLORIDE. CHLORINE AND AROMATIC HYDROCARBON.Take care with ALCOHOL based SPRAYS (20% - 40% alcohol). They lead to tarnishing and small cracks in the plastic, and do not provide the necessary cleaning prior to disinfection. Disinfecting SPRAYS may be used, in accordance wih the manufacturer recommendation, from a distance of 30cm of the device, avoid the accumulation of the product in liquid form. Please contact the appropriate service responsible for cleaning and disinfecting products in your establishment for further details. Storage The device should be stored in a dry, cool place. In case of prolonged storage, the battery should be disconnected via the battery access flap situated underneath the device.This should be done by a qualified technician. Humidity: 10% to 90%, no condensation. Fully recharge the battery before using the device to avoid any risks caused by micro power Use of the internal battery This device is provided with NiMH battery. When the device is disconnected from the mains, it automatically switches to battery mode. Before starting for the first time, charge the battery for approx. 5 hours by connecting the power supply cord without using the device. In case of frequent mains operations, battery life may be decreased. To limit this risk, it is recommended to use the device on the battery mode, approximately every 4 weeks, until getting a battery pre-alarm signal. Diagnostic Troubleshooting guide Problem Cause Action End of infusion detected too early (at approximately 10ml). No end of infusion pre-alarm and alarm The installed syringe doesn't correspond with the selected syringe. Replace or confirm the right syringe brand.

If the keypad is unlocked during the infusion, it will lock again automatically after a time- out. The screen displays 5. Press OK to confirm. Switching from Night Mode to Day Mode You can switch to day mode as follows: 1. You can view the infusion history as follows: 1. Press 2. Press the arrow keys to select 3. Press enter. 4. You can view flow rate history as follows: 1. Press 2. You can view pressure history as follows: 1. Press 2. Press the arrow keys to select 3. You can view the remaining time before clinical information display as follows: 1. To return to the normal menus, power off then power on again. Option Descriptions Four different option groups are available on the pump. Communication via Wi-Fi The Wi-Fi option allows the pump to connect to a hospital information system without cables. To activate or deactivate the Wi-Fi module, see section 8.3, page 77. For more information on the Wi-Fi module, refer to the technical manual. Perform this user test before each use of the pump. 1. Check the external appearance of the pump for the absence of cracks or other visible damage. When an alarm is triggered, a message is displayed on the pump screen. We recommend that the user stand in front of the pump to read the message before acknowledgment. The time remaining is less than the defined time duration (adjustable between 1 and Near end of volume Medium (!!) 30 minutes), and the remaining VTBI until the limit !! volume limit has dropped to less than 10% of the syringe capacity. Information The upper soft limit is exceeded, according to Upper soft max signal the drug settings defined in the drug library. Information The lower soft limit is exceeded, according to Lower soft min signal the drug settings defined in the drug library. Temperature increase.This will prevent the back-up of IV fluid or medication into the gravity line.

Warning If the device is not used for an extended period (longer than 2 months), it is recommended that the battery be removed from the device and put. Range of settings and default values may be adjusted in the pump options (Basic Profile) or a compatible DERS (custom profiles). Increment rules may be modified with a compatible DERS (custom profiles). The battery charges when the pump is connected to AC power supply. Before starting for the first time, charge the battery for approximately 6 hours by plugging in the power supply cord with the pump powered off. Information If communication with the wireless network is interrupted, the pump can be used as intended. For more information, contact your Fresenius Kabi sales representative. Data integrity and quality of service are inherent in the design. The system should be ensured and maintained by a qualified and trained technical user, or a Fresenius Kabi sales representative. If such use is necessary, this equipment and the other equipment should be observed to verify that they are operating normally. Please refer to your competent Health Authority or local Fresenius Kabi sales representative to check availability on your market. Agilia Connect Infusion Devices detailed intended use are available on request. Discover everything Scribd has to offer, including books and audiobooks from major publishers. Start Free Trial Cancel anytime.Browse Books Site Directory Site Language: English Change Language English Change Language. A collection of service manuals, tutorials and descriptions of medical equipment. Fresenius Injectomat MC Agilia. With Injectomat Agilia you can monitor your syringe pump at Injectomat Agilia offers interactive navigation via www.fresenius-kabi.com Maintenance Tools.12 Dec 2016 Infusion Technology - Fresenius Kabi USA Fresenius kapi injectomat agilia service manual - EBME.

MAX 4376 voltage regulator is out of order. Check the battery charging voltage Replace the power supply board if necessary. Replace the battery. Battery is totally discharged. The device turns ON or turns OFF alone. Defective keyboard. Power supply board is out of order. Some keys of the keyboard do not work. Defective keyboard. Check and replace the keyboard if necessary. After a fall Mechanical elements are damaged. Check the status of the housings and the mechanical system. Modifications may be done in future editions.We are a non-profit group that run this website to share documents. We need your help to maintenance this website. The user must adhere to the instructions specified in this IFU. Failure to adhere to these instructions may result in damage to the equipment, injury to patients or injury to users. Typical initial training duration: 1 hour. It is recommended that users attend a refresher training session of about 20 minutes every year. For training, contact your Fresenius Kabi sales representative. Information For more information on using the device in specific conditions, contact your Fresenius Kabi sales representative. Near Power Cord Inlet Warning Near RS232 Communication Port See section 9, page 78. Infusion in Progress (Custom Profiles) This symbol is displayed when the pump is infusing a drug customized with infusion limits customized with a compatible DERS. Infusion Stopped STOP remains in the center of the screen until the user starts the infusion again. By default, factory settings include only 1 profile (Basic Profile). Custom profiles can be created and loaded to the pump using a compatible DERS. Custom profiles feature a specific pump configuration and a drug library. For example, make sure to limit flow rates for sensitive populations. Do not stack the pump with equipment other than those recommended. Using the Rotating Pole Clamp The rotating pole clamp is located at the back of the pump.

Preparing and priming the syringe and the extension set Section 12.2, page 87. Powering on Section 5.3, page 28. See section 4, page 23. 2. Plug the pump into the AC power supply. See section 16.1, page 103. 3. Before starting the pump for the first time, you must charge the battery for approximately 6 hours. The symbol shows three different charge levels: If the pump height is raised relative to the distal tip of the catheter (e.g., during patient transport), the increase in height of the syringe pump can result in a temporary increase in fluid delivery or bolus until the flow rate. A clinical advisory message may appear, if one is configured for the selected syringe. 4. A clinical advisory message may appear, if one is configured for the selected drug. 3. Press OK to acknowledge the clinical advisory message and continue programming, or C to change the drug.The VTBI and the flow rate are automatically calculated based on dose and duration settings. Infusion Duration At the current rate, the remaining infusion time in hours and minutes. To restart the infusion, first confirm or modify the programming settings, then start the infusion. The flow rate is calculated automatically. Flow rate Dose Rate 3. End of infusion settings are configurable with a compatible DERS (custom profiles), or in the pump options (Basic Profile). When the limit is reached, an alarm is triggered. 1. Access the Volume Limit menu, see section 7.12, page 66. Flow rate Dose Rate 2. Always select the automatic prime function for life-sustaining drugs. 6.11.2 Pre-programming the Pump You can program the pump before installing the syringe. 1. Warning To avoid the presence of air and to minimize the amount of time it takes the pump to recognize an occlusion and generate an alarm while infusing at low rates (e.g., less than 5 mL per hour, and especially flow rates less than 0.5 mL per hour):. The keypad will lock automatically at infusion start.

Fresenius Injectomat Agilia Service Manual User Manual Here 1 2 Hi, frendis i need a servive manual for Fresenius kapi injectomat agilia.. I also need the service manual - Fresenius Kabi Injectomat Agilia. Would you be so. Opportunity Makers. Your Faculty. Opportunity Makers. Your Faculty. Students receive the same guidance, expertise, and access to vast professional networks. While you may be learning online, our faculty is just on the other side of your screen, fully committed, and engaged in your success. All Rights Reserved. Intended use Injectomat Agilia is This pump must be Precautions to The symbol vis Injectomat Agilia wof the medical devicesradiations avoids the uis placed near devicedistances between equ The device must noshould always be used The device can be etc. If you wish to use tmust be used in a horiz The physiological esyringe. Check that thealarm setting times in r In case of unexpecalarm, to stop infusionChapter 6).Its immunity makes it possible to ensure correct operation.