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File Name:Braun Infusomat Space User Manual.pdf

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Valid for software 586U. Caution: Do not lean on pump Pole clamp when attached to pole.Turn black knob counter clockwise to release from IV pole. To disconnect, push green locking button of the upper pump and slide lower pump out. Caution: A maximum of three B. Braun Space pumps can be stacked together when used with the Space Pole Clamp (speed clamp). Power supply holder The Space Pole Clamp (speed clamp) can. See accompanying documents.After each soft- ware update, the user must refer to the Instructions for Use to review changes to the device and software. If the down arrow is pressed on the above screen, the pump displays the previous value i.e. Insure silicone segment is not stretched or twisted, stars on tubing must be in straight line and line loading guide should not be twisted. Anti-Free Insert the green anti-freeflow clip in Flow the green slot, in the direction indi- clip insertion cated by the arrow, until the opening. Note: Pump automatically powers up in the drug library for all new infusions. When selecting drugs, in the library drug names will only appear if marked for that mode in the drug library file. In addidtion a drug may be marked to deactivate SECondary mode. Example 2: Drug with a lower hard limit of 0.2 g Current value is 0.3 g. When the is pressed once again with the cursor in the hundreds column the hard limit message is displayed and remains until confirmed by pressing k. Note: Programming of infusion parameters may be done prior to loading the IV line by pressing from this screen. This will re- quire re-programming the therapy when a care unit change is done prior to beginning the infusion.Home screen may be ac- cessed from run screen by pressing key. Note: Default values may be present when set in drug library, in this case the editor screens do not appear, confirm values and press to begin the infusion or press arrow to edit default values. Note: PRIM will appear in upper left of screen to indicate PRIMary is running.
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When pump is stopped, PRIM appears next to home symbol. The 8 inch interval is measured from the bottom of the SECondary bag to the top of fluid level in the PRIMary. Dose over Time run screen will indicate drug name and count down remaining time.When all are checked press to confirm and then press to begin infusion. Note: Reminder to check bag height and unclamp SEConday will appear, press again to begin SECondary infusion. Note: When default values have been set in the Drug Library there will not be a prompt to enter values. Values may be edited by scrolling to the parameter and pressing the arrow key. Manual bolus is limited to 10 seconds. The pump may be set to emit an audible tone every 1ml of solution delivered. The soft limit warning will be shown requiring an over ride or new programming to proceed as in Section 1.2. Pump will display message if Care Unit was not changed because drug or drug concentration is not available in new Care Unit or hard limits are exceeded. Rate titration will result in re-calculation of VTBI. 1.12 IV Line Change and New Therapy Start Note: Always close roller clamp and disconnect the line from the patient before changing a line to avoid inadvertent free flow. Note: When pump is powered up user will be prompted to continue last infusion, answering No returns to B. Braun landing page. Note: Pump cannot be powered off with IV line inserted. Press while pump is running to access home menu. All menus may be accessed while the pump is running except the SECondary menu. Features displayed in the menus are determined by your facility and set in the service program. Note: Pump may be set up in service program to prompt “Use Dose Rate Calculator?”. A third level may be set in the drug library by drug. A four digit code (default setting “9119”) must be entered within 20 seconds to prevent a data lock alarm.
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If the wrong code is entered four times the pump will go into an audible alarm, the yellow LED will light, and the pump display indicates invalid code. This rate is used for manual bolusing. For a programmed bolus, this rate will be converted to a time in the time editor screen if no default bolus rate has been set in the drug library and may be changed by adjusting the time. Alarm- Audible Optical signal Staff call User confirmation type signal Red LED Yellow LED Text Device flashes device alarm Follow the instruc- Alarm and alarm tion on the display to press k. After that, the pump goes into an opera- ting alarm. Operating alarms: Operating alarms immediately stop the infusion. An audible tone sounds, the red LED flashes and a staff call is activated (optional). The air bubble size can be set between 0.02 - 0.3ml in increments of 0.01. An acoustic tone sounds in 20 seconds, the display states “Value not confirmed“, the yellow LED is constantly on and a staff call is activated (optional). A file symbol will flash alternately with the wireless antenna symbol on the top of the pump display when a new file is available. New drug library has been activated on pump. Note: Soft Limit alert will be issued if value exceeds any soft limits set in drug library, soft limit may be overridden or value re-programmed per institutional policy. SECondary Orders: Orders received after PRIMary has been set will be for SECondary infusions, follow prompts on screen to stop the PRIMary to accept the SECondary order. The wireless battery module contains a wireless transceiver module to allow data transmission during these transports or when connected to AC power. Fire or chemical burn hazard if battery is mishandled. To avoid possible injury. Open the cover of the battery compartment (see ch. 1.12), unlock the battery by sliding the green hook and pull out the battery using the metal handle.
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Replace the Battery Pack SP in the battery compartment, lock it with the green hook and test the proper placement by pulling the metal handle. Signal strength: The signal strength shows the quality of the connection. In this case it is necessary to per- form a battery maintenance. To initiate the discharge process the message “Battery maintenance“ and the will be displayed after switching the pump off. Deviations from the technical data of the pump cannot be excluded if lines (disposables) other than B.Braun approved sets are used. Trumpet Curves Measured values for second hour in each case. The housing of Infusomat Space, the line guide cover and the IV line guiding areas may be disinfected with EPA registered hospital disinfectants containing 1-propanol, isopropyl alcohol, ethanol or didecyl dimethyl ammonium chloride. Do not allow moisture or detergents to come into contact with the electrical connections of the device (P2 or P3 connectors) or any device openings. For further information contact your B. A maximum of three plugs can be stacked upon each other in P2 socket.A Returned Materials Authorization number will be provided. Carefully pack the pump (preferably in the original packing), and ship it prepaid to the address below. B. Braun cannot assume any responsibility for loss or damage to returned instruments while they are in transit. Valid for software 686J. To remove, press release button on frame, push handle down and pull PoleClamp backwards. After each software update, the user is required to inform himself about the changes to the device and accessories in the instructions for use. Do not use enteral fluids for intravenous infusion as this may harm your patient. For this reason only use disposables dedicated and labelled for enteral nutrition. They need to be fully aware of the available literature for any parameter set used in association with a drug and need to refer to the prescribed information for rate and dosing limits.
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The desired information can be selected by using and will be displayed permanently thereafter (e. g. drug long name, etc.). has been pressed while the pump is infusing. Check the equipment for completeness and damages. Fill the bottom part of the drop chamber by max. Make sure that the line is routed straight. At first, route the line through the upstream sensor. Then, insert the two-hole clip. In the next step, attach the white clip without twisting the line. Target: VTBI 3.) Infusion with time limit Enter rate and time: The infusion volume will be calculated and displayed on the bottom of the display. In order to purge the line at any time while the pump is stopped press Answer the following question by pressing in order to start the purge process. Navigate through the menu using to check parameters.The therapy can be started now with in case all values are defined. For Propofol the user can choose between two parameter sets. The parameter sets used for these drugs are (Not all parameter sets allow effect-site targeting):. Setting up the pump For TCI a drug list with at least one drug activating the profile TCI is necessary. The drug list in this version is pre-defined. By this the conditions for an effective and safe therapy are defined. Above the pump the piggyback-infusion line is connected with a Y-connector to the administration set. The secondary infusion is supposed to be located approx. 20 cm higher than the primary infusion. The user defines a series of intervals (max. 12 intervals) by certain parameters (rate, time, volume) for each cycle. The pump automatically gives each programmed period, one after the other. Example: Program Mode should only be performed by an experienced user being familiar with the principles of the Program Mode function and properly trained in using the present. Take care to set the VTBI in the correct relation to the volume of one Cycle. VTBI may needs to be adjusted after Changing the intervals.
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The Main menu informs about the current interval. The configerd paramters can be checked by Program Parameter Menu in Main. Before using Dose Over Time contact your local B. Braun representative. Starting Dose Over Time via Drug Library: Note: Dose Over Time settings have been configured in the Drug List Manager before and have been uploaded into the pump. For this reason the remaining time is shown big digits in menu Run. The parameter in the lower left corner can be scrolled. Set to Rate when leaving the pump. Note: It is always possible to press the key in the Run Menu and edit or. To edit a menu item, select “Options” in the Main Menu and press l. Then select desired function with and follow the Instructions for Use as described. Alarm- Audible Optical signal Staff call User confirmation type signal Red LED Yellow LED Text Device flashes flashes device alarm Press and follow Alarm and alarm the instruction on the code. When pushing on the battery cover listen for “click”. “Standby time expired“ The set standby time has ended. Set new time or continue with previously set therapy. “No battery inserted“. Examine the line for damage and check the drop chamber. “Data were reset” Therapy and pump settings could not be restored. These hints disappear after a few seconds and don't need to be confirmed. For optimal treatment of the battery, the device is equipped with protection against overcharge and deep depletion. The battery pack is charged by the pump during connection to mains. Consider disposal directions. Battery maintenance: To accurately balance the battery capacity a cyclical battery maintenance is necessary. The pump asks the user to perform a battery maintenance every 30 days. The battery maintenance mode detects a possible capacity loss (e.g. They allow for the following: The delivery behaviour or delivery precision is essentially influenced by the type of the disposable used. These technical data can change when using set configurations.
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When taking care of disposing of disposables as well as infusion solutions, please consider the applicable hygiene and disposal regulations. PoleClamp SP (8713130) A maximum of three B. Braun Space pumps and one SpaceControl can be stacked together when used with the PoleClamp SP.The connection of the Drop Sensor SP on the pump is located at the rear of the device, in the lower left corner. Sign in Forgot Password. My Bench Close Sign In Not A Member. Sign Up Join MedWrench OK name type Receive Summary Emails. The lightweight large volume pump allows for flexibility and easy transport within a number of care settings. The system is designed for higher acuity care facilities, offering a large drug library as well as the capability to build up to 24 pumps in a single bedside tower. FORUMS View All (22) Ask a New Question 2 Replies -Tonyvision3 3 months ago 3 months ago error code 2035 Hello everyone.Compagny says to just send it back. Breakage may occur when the IV set anti free flow clip catch This site uses cookies. 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. Discover everything Scribd has to offer, including books and audiobooks from major publishers. Start Free Trial Cancel anytime. Report this Document Download Now save Save Operating Manual Infusomat space.pdf For Later 0 ratings 0 found this document useful (0 votes) 139 views 82 pages Operating Manual Infusomat space.pdf Uploaded by amirali.bme4527 Description: Full description save Save Operating Manual Infusomat space.pdf For Later 0 0 found this document useful, Mark this document as useful 0 0 found this document not useful, Mark this document as not useful Embed Share Print Download Now Jump to Page You are on page 1 of 82 Search inside document Browse Books Site Directory Site Language: English Change Language English Change Language. Instructions for Use. US Valid for software 586U.
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It is recommended that all pumps at your institution are equipped with. The space saving, high performance infusion pump for standard infusion lines. Interactive content. Use mouse to control picture. Excellent readability: Graphic display with high resolution and contrast. Intuitive: Cell phone like operation. Space Smart Batteries come with 12 month warranty. With HiBaSed, you can program your. It only encompasses the pages that describe. All pre-owned medical equipment is patient ready equipment and is. Reload to refresh your session. Reload to refresh your session. Sign in Forgot Password. My Bench Close Sign In Not A Member. Sign Up Join MedWrench OK name type Receive Summary Emails. 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. Drug information can be subdivided in 50 cae units and up to 16 Patient Profiles. A complete customizable drug library, with limits and personalized settings for individual drugs assist an easy and safe stay in hospital. Check out common pitfalls and strategies for prevention.Indications of use may also vary by country and region. Please contact your country representative for product availability and information. Product images are for reference only. Cookies enable you to enjoy certain features such as playing videos or displaying personalized content. Cookies allow to tailor messages and display advertising to your interest (on our site and others). They also help us to understand how our site is being used and allow us to further improve our websites.Cookies enable you to enjoy certain features such as playing videos or displaying personalized content. Cookies allow to tailor messages and display advertising to your interest (on our site and others). They also help us to understand how our site is being used and allow us to further improve our websites.Without these the website cannot be used as intended.
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Among other things, they ensure provision of the correct functionality when a page is changed from http to https and therefore that increased security requirements are met. Your consent is not required for the use of essential cookies.These cookies do not store any other information. They are used simply to increase user-friendliness and to tailor websites more specifically to the individual user. This information is also stored only in anonymized form.They are used to present the user with relevant and tailored advertisement. Infusion syringe pump Perfusor Space............ 0871 3030 This Service Manual is available under the following part number: Designation Part No. Service Manual Perfusor Space, English........... 8713 9020 Languages of this Manual The Service Manual for this unit can be supplied in the followinglanguages: Designation Part No. The possession of this manual does not authorize the performance of service work.Service tasks may only be executed by persons, who - have received appropriate training on the system fromB. Braun - are included in the revision service - possess the necessary test equipment and mechanical aids,and - fulfill the personal requirements (training and knowledge). Technical Safety Checks The user is obliged to perform or to have performed the TechnicalSafety Checks on those medial products for which these checkshave been prescribed by the manufacturer and to carry them outaccording to the indications of the manufacturer as well as thegenerally approved technical standards while adhering to theperiods stated ( 6 MP BetreibV). B. Braun also recommends training on the Technical SafetyChecks, or to perform at least the steps indicated in the currentversion of the manual, as: - the TSC requires that the instructions in the manuals areobserved - the manuals are a reference for measurements - depending on the unit type, the Service Program must becalled which may lead to a dangerous unit condition in caseof inappropriate operation.
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Furthermore, a special serviceconnector may be necessary. Current Versions This manual version corresponds to the state when the manualwas written. B Braun reserves the right to make technicalmodifications. The state of the revision is indicated by the indexnumber in the footer of every page. Revision Service The possession of this manual does not automatically meaninclusion in the revision service. You will be included in therevision service after: - technical training by B. Braun Melsungen or - a written order placed with the sales department of B. Braun(fee required). Important Preliminary Remarks 0 1.21.0 Responsibility of the Manufacturer The manufacturer, person who assembles, installs or imports the device can only be held responsible for safety, reliability andperformance if - mounting, enhancements, new settings, changes or repairsare carried out by duly authorized persons, - the electrical installation in the corresponding room meetsthe requirements of the VDE 0107, VDE 0100 part 710 orIEC 60364-7-710 and the national standards, - the device is used in accordance with the instructions for useand the Service Manual, - the Technical Safety Checks are performed at regularintervals, - a current manual which corresponds to the revision state isused when carrying out maintenance, repair and service, - the service technician takes part in the revision service, - the technician has participated in a technical training coursefor the specific B. Braun unit. Quality Management B. Braun is certified in accordance with DIN EN ISO 9001 andISO 13485. This certification also includes maintenance andservice. The unit has the CE label. Checks and Repair Training may only be performed by B. Braun. The possession of themanual does not authorize the performance of repairs. Theinstructions on electrostatic sensitive components (ESDstandards) must be observed. After repair a device check or diagnosis is to be carried out.

Notes on ESD Semiconductors can be destroyed by electrostatic discharge.Especially MOS components can be damaged by interference fromelectrostatic fields, even without discharge via contact. This typeof damage is not immediately recognizable. Unit malfunctionscan even occur after a longer period of operation.0 - 6 Perfusor Space, 1.2 gb Important Preliminary Remarks 0 1.2 Each workstation must be equipped according to therecommendations with the necessary static protective measures,if ESD components or boards are handled. Each workstation must be equipped with a conductive tablesurface. The conductive surface, the soldering iron or thesoldering stations must be grounded via protective resistors. Chairs must be of antistatic design. The floor or floor mats shouldbe of electrically conductive material. Personnel must wear conductive wristbands which are connectedto a central ground potential via protective resistors, e.g. theground contact of a wall outlet. Furthermore it is recommendedthat personnel wear cotton clothing and electrically conductiveshoes to prevent electrostatic charge. Spare Parts and Test Equipment Only use original spare parts from the manufacturer. Do nottamper with assembly groups which can only be exchangedcompletely. The spare parts required are listed in Section 9. Service personnel are responsible for the calibration of their testequipment. Original test equipment can be calibrated at theworks of B. Braun. Further information is available upon request. Setting Off Additional notes and warnings are set off as follows: Note Is used for additional or special notes concerning information andworking steps. CAUTION Is used for working steps which may result in damage to the unit,system or to a connected device.Click with the mouse button on a referenceto jump to the corresponding source. Menu commands are described as:Menu File.0 - 8 Perfusor Space, 1.2 gb Important Preliminary Remarks 0 1.

2 List of Abbreviations Abbreviations which are not generally known, but are used in this manual, are listed below. Continued use of our website without having changed your browser settings confirms your acceptance of these cookies. For details please see ourDrug information can be subdivided in 50 care units and up to 16 patient profiles. Indications of use may also vary by country and region. Please contact your country representative for product availability and information. Product images are for reference only. It is possible that some links will connect you to content onlyIn the case of any discrepancy in meaning, the English version is considered official. Thank. These routes include intravenous, intra-arterial, subcutaneous, epidural and enteral. Features and Benefits All other currencies are for display purposes only. Exchange rates may vary. Displayed cost does not include customs fees. Continued use of our website without having changed your browser settings confirms your acceptance of these cookies. For details please see ourWeighing only 3 pounds, it’s smart, compact design allows for flexibility and easy transport within all care settings. The Infusomat Space packs state-of-the-art versatility that promotes efficiencies in the ICU, CCU, NICU, PICU, OR, Emergency Department or Outpatient Care settings. To achieve this, B. Braun worked with Healthcare Human Factors, a global leader in developing best practices for human factors testing in healthcare. It was one of the first infusion pumps to be cleared by the FDA’s new human factor and usability engineering process. Call: 866-468-9558 Up to four Space infusion pumps can be placed into one docking station in any configuration. Removal is just as quick and easy The power is always supplied to the system via a single cable Alarms and pre-alarms will be indicated visually and audibly. The integrated carry handle converts the B.

Braun SpaceStation into a portable unit ReNew handles our needs efficiently and are always willing to go the extra mile.” Web Credits. Warranty: 1 Year. Lead Time: Certified Refurbished: Usually Ships in 1-2 Weeks. Factory New: Backordered. Expected to ship by July 1st. Note: This Pump requires signage of the End User License. Designed for acute care adult and pediatric facilities, the B. Braun Infusomat Space Infusion Pump features a compact design (weighs only 3 lb) that allows for improved flexibility and easy transport within all care settings. Emphasizing intuitive workflow and navigation, this top-of-the-line pump promotes efficiencies in the ICU, CCU, NICU, PICU, OR, Emergency Department or Outpatient Care settings. It has undergone more than 100 hours of usability testing and is one of the first infusion pumps to be cleared by the FDA's new human factor and usability engineering process. B. Braun Infusomat Space Infusion Pump Features Same user interface on all SpaceTM pumps. Compact, light-weight design. Vertical stacking saves space. KeyGuard, non-numeric keypad. Independent modularity. Wireless interoperability. Independent Modularity: A microprocessor in each pump helps to prevent channel confusion and catastrophic pump failures. Easily Stackable: Vertical stacking takes less space for increased versatility in certain healthcare settings. KeyGuard: Non-numeric keypad with simple arrows designed to prevent manual programming errors related to zero vs decimal entry. Intuitive Universal User Interface: Helps to reduce staff training time. Extensive Drug Library: Includes customizable hard and soft limits and clinical advisories. Wireless Integration: Allows for complete interoperability. Alarms: Audible, clearly visible and differentiated using different tones. B. Braun Infusomat Space Infusion Pump Specifications Classification (acc. Classification (acc.Moisture Protection: IP 22 (drip protected for horizontal usage).

External Low Voltage: 11 - 16 V DC via Connection Lead SP. 12 V or via SpaceStation. Time of Operation: 100 (continuous operation). Operating Conditions: Relative Humidity: 30 - 90 (without condensation). Storage Conditions: Relative Humidity: 20 - 90 (without condensation). Recharging Time: Approximately 6 hours. Weight: Approximately 1.4 kg. Dimensions: 214 mm x 68 mm x 124 mm. (8.4 inches x 2.6 inches x 4.8 inches). Volume Increments: 0.1 - 99.99 ml in increments of 0.01 ml. 100.0 - 999.0 ml in increments 0.1 ml. 1000 - 9999 ml in increments 1 ml. Administration Set Change Interval: Pumping accuracy is maintained for a minimum of 96 hours. Max. Volume in Case of Single Fault Condition: For incorrect dosages of 1.4 ml due to malfunctions of the device the pump will automatically shut off.Sign up now. Its compact and intuitive design allows for flexibility and easy transport within a healthcare facility, promoting efficiencies in hospital or outpatient settings. The Company is committed to eliminating preventable treatment errors and enhancing patient, clinician and environmental safety. To learn more about B.Braun visit www.BBraunUSA.com Learn more. Leading the way into the future, this system meets all demands of an outstanding safety concept required for both infusion therapy and patient safety during treatment. That's what I need a vendor to take care of.

The conductive surface, the soldering iron or the soldering stations must be grounded via protective resistors. Chairs must be of antistatic design. The floor or floor mats should be of electrically conductive material. Personnel must wear conductive wristbands which are connected to a central ground potential via protective resistors, e.g. the ground contact of a wall outlet. Furthermore it is recommended that personnel wear cotton clothing and electrically conductive shoes to prevent electrostatic charge. Spare Parts and Test Equipment Setting Off Only use original spare parts from the manufacturer. Do not tamper with assembly groups which can only be exchanged completely. The spare parts required are listed in Section 9. Service personnel are responsible for the calibration of their test equipment. Original test equipment can be calibrated at the works of B. Braun. Further information is available upon request. Additional notes and warnings are set off as follows: Note Is used for additional or special notes concerning information and working steps. CAUTION Is used for working steps which may result in damage to the unit, system or to a connected device.When the Service Manual is stored as pdf-file, these references are displayed green. Click with the mouse button on a reference to jump to the corresponding source. Menu commands are described as: Menu File. 0-8 Infusomat Space, 1.0 gb Application for a technical training course must be made via the responsible representative.The medical specialist must decide on suitability for application on the basis of the warranted properties and the technical data. System Overview Fig.: 1-1 Space system Legend to fig. 1-1: ItemDesignation 1 SpaceCover 2 Infusion pump Infusomat Space 3 Infusion syringe pump Perfusor Space 4 SpaceControl 5 SpaceStation 5 The Space system is a modular design of modern infusion technology for stationary, mobile or private use.