Eickemeyer InfusoVet IP User Manual

Infusion pump

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INFUSOVET IP

INFUSION PUMP

USER MANUAL

Item no. 402085

TELEPHONE +49 7461 96 580 0

www.eickemeyer.com

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Page 1 INFUSOVET IP INFUSION PUMP USER MANUAL Item no. 402085 TELEPHONE +49 7461 96 580 0 www.eickemeyer.com...
Page 3 Release date: 2022-05 Revision: 2.0...
Page 4 Preface Manual Purpose This manual contains the instructions necessary to operate the product safely and in accordance with its function and intended use. Observance of this manual is a prerequisite for proper product performance and correct operation and ensures animal and operator safety.
Page 5: Table Of Contents
Contents Preface ..........................II 1 Safety ......................... 1-1 1.1 Safety Information ....................1-1 1.1.1 Dangers ...................... 1-1 1.1.2 WARNING ....................1-2 1.1.3 CAUTION ....................1-3 1.1.4 NOTE ......................1-4 1.2 Equipment Symbols ....................1-5 2 Overview ........................2-1 2.1 Description ......................2-1 2.1.1 Indications for Use ..................
Page 6 4.2 Operational Procedures ..................4-2 4.2.1 Turn on the Pump ..................4-2 4.2.2 Load the Infusion Set ................. 4-2 4.2.3 Change the Infusion Set ................4-4 4.2.4 Change the Infusion Bottle (Bag) ............... 4-4 4.2.5 Select Infusion Set Brand ................4-4 4.2.6 Infusion Mode .....................
Page 7 7.4 Alarm Countermeasures ..................7-3 8 Battery ........................8-1 8.1 Battery Performance Optimization ................ 8-2 8.2 Check the Battery ....................8-2 8.3 Battery Recycling ....................8-3 9 Preservation and Sanitation ..................9-1 9.1 Description ......................9-1 9.2 Cleaning ....................... 9-1 9.3 Disinfection ......................
Page 8 C.3 Parameters ......................C-1 C.4 System Time ....................... C-2 D Alarm Information ....................D-1 E Symbols and Terms ....................E-1 E.1 List of Units ......................E-1 E.2 List of Symbols ..................... E-2 E.3 List of Terms ......................E-2 E.4 List of Unit Conversion ..................E-4 F Toxic and Hazardous Substances or Elements ............
Page 9: Safety
Safety 1.1 Safety Information The safety statements presented in this chapter refer to basic safety information that the operator must pay attention to and abide by when using the veterinary infusion pump. There are additional safety statements in other chapters or sections, which may be the same as or similar to the following, or specific to particular operations.
Page 10: Warning
1.1.2 WARNING WARNING Device, cables and accessories must be inspected before use to  guarantee their normal and safe operation. This equipment can only be connected to the socket with ground  protection. Please adopt a rechargeable battery instead of the socket as the power supply if the socket is not provided with a ground lead.
Page 11: Caution
infusion sets, please make sure to confirm relevant infusion performance (such as accuracy, bubble and pressure) on veterinary infusion pump, and contact the company for calibration service, the infusion sets can only be used after confirmation, otherwise we is not responsible for infusion performance (such as accuracy, bubble and pressure) and relevant alarm function of the veterinary infusion pump.
Page 12: Note
potential interference sources because of their high-intensity electromagnetic radiation. Before the equipment is connected to the power supply, check that the  voltage and frequency of the power supply match the specifications on the label or in this Operator’s Manual. Please install and carry the equipment correctly to protect the ...
Page 13: Equipment Symbols
1.2 Equipment Symbols The equipment you purchased may not provide you with all the following symbols. Consult instructions for ON/OFF Alternating current power Battery supply (AC) Alarms AUDIO PAUSED Clear/Back Start Bolus Confirm Stop Menu Move up/Increase Move down/Decrease Move left Move right Infusion set Caution...
Page 14 Protected against solid foreign objects with a Environmentally- diameter no less than friendly use periods of IP34 2.5mm and protected electronic products (20 against spraying liquid years) water Temperature limit CE mark NRTL certification Recycle mark Atmospheric pressure Humidity limitation limitation Serial number The following definition of the WEEE label applies to EU member...
Page 15: Overview
Overview 2.1 Description 2.1.1 Indications for Use The veterinary infusion pump is used in conjunction with the infusion set to control the dose of liquid infused into the animal’s body. This veterinary infusion pump is expected to be used in institutes or units with healthcare capabilities.
Page 16: Host
2.2 Host 2.2.1 Front View Alarm light The alarm light indicates different alarm levels in different colors and flash frequencies, please refer to Chapter 7 Alarms for details . Display Used for displaying infusion parameters and relevant content. <CLEAR/BACK> Under non-setting status, indicate to return to the previous menu or ...
Page 17 AC/DC indicator light On: The pump is connected to an AC/DC power supply (including  shutdown). Off: The pump is not connected to an AC/DC power supply.  Battery indicator Steady green indicates that the battery is charging.  Flashing indicates that the battery is providing power. ...
Page 18: Front View With The Door Opened
2.2.2 Front View with the Door Opened Liquid check clip button Liquid check clip Infusion set slot...
Page 19: Rear View
2.2.3 Rear View DB9 interface, which combines the following interface functions: DC power input interface  RS232 interface  Nurse call interface  Alternating current power supply (AC) port Connected by three-core-type power cord and AC power source. Drop sensor interface Pole clamp Product label...
Page 20: Screen Display
2.3 Screen Display This veterinary infusion pump has a monochrome LCD screen. The display information comprises two main parts: Parameter area Display battery icon, every parameter and the parameter value of the current screen, etc. Prompt bar Display run icon. The run icon on the screen displays the running operation: The icon indicates normal running.
Page 21: Installation And Setting
Installation and Setting 3.1 Installation WARNING Equipment assembly and refit (including correct protective grounding  connection) during life period must be carried out by maintenance technicians whom are trained and licensed by the manufacturer, and evaluated according to the specified IEC60601-1. Please contact the company if you have any queries.
Page 22: Out Of Box Audit (Ooba)
NOTE This equipment is in accordance with the EN 1789:2007+A1:2010  standard. It can be fixed on cross bar (square cross bar: 10 x 25 mm) or vertical bar (round vertical bar with diameter size of 15-38mm) of ambulance with advanced pole clamp. Please refer to 3.1.3.2 Advanced Pole Clamp (Optional) for detailed operation of advanced pole clamp.
Page 23: Mount The Clamp
The operating environment should also be appropriately protected from noise, vibration, dust, and corrosive, inflammable or explosive substances. If installed inside the equipment case, a sufficient space before and after the equipment case should be ensured to facilitate operation, maintenance and repairing work.There should be a 2" (5 cm) gap around the veterinary infusion pump to ensure that air can circulate freely for a better cooling effect.
Page 24: Advanced Pole Clamp (Optional)
2. Tighten the pole clamp clockwise to firmly fix the device on the IV stand (round vertical bar with diameter size of 15-32mm). 3.1.3.2 Advanced Pole Clamp (Optional) Press the button of pole clamp, horizontally or vertically adjust pole clamp, the button will pop-up after loosening the pole clamp.
Page 25: Connect The Ac Power Source
3.1.4 Connect the AC Power Source Please confirm to use the original three-core-type power cord. Insert one end of the power line into the AC socket on the back panel of the veterinary infusion pump. Insert the other end of the power line into the matched three-plug connector connecting to the AC power.
Page 26 Firmly insert the signal line of drop sensor into the connecting port on the right side panel of the pump. Clip the drop sensor to the drip chamber, making sure that the drop sensor is above the surface of the liquid. Press to start the infusion.
Page 27: Conventional Settings
NOTE The surface of the liquid in the drip chamber must be lower than the  drop sensor, which should be between 1/3 and 1/2 of the drip chamber. The positioning block of the drip chamber must be inserted vertically ...
Page 28: Set Date And Time
3.2.3 Set Date and Time Select [Main Menu]→[System Date and Time]. Set [Time] and [Date]. CAUTION Please check the system date and time to keep accurate records in the  History function. 3.2.4 Adjust Volume Select [Main Menu]→[Volume]. Select [Volume]:1-8.1 for the lowest volume;8 for the highest volume. 3.3 Restore Factory Default During operation, you may change some settings in some situations.
Page 29: Basic Operation
Basic Operation 4.1 Infusion Flow Chart Press to activate and turn on the pump, the Turn pump on pump will run start-up checks and display the start- up screen; Load infusion set Please refer to 4.2.2 Load the Infusion Set; Select according to the infusion set brand currently Select brand being used;...
Page 30: Operational Procedures
4.2 Operational Procedures 4.2.1 Turn on the Pump Please turn on the device as the following steps: Perform a safety inspection referring to 10.1 Inspection before turning on the pump. Press , the system will initiate the self-test and the screen will display the [System Self-test] interface: The system will give out a sound "di"...
Page 31 2. Pull the free flow clamp button upward 1. Pull the door holder and open the door. left, and open the free flow clamp. 3. Load the set, confirm it is firmly loaded into 4. Close the door, the interface will enter the tube slot.
Page 32: Change The Infusion Set
reloaded. WARNING The infusion set should be firmly loaded into the slot, and not jutting on  the outside of the slot. Before using this veterinary infusion pump, the veterinary infusion  pump, infusion set, and other accessories should be loaded correctly. 4.2.3 Change the Infusion Set Follow the steps below to change the infusion set: To prevent animal injury due to free flow, before changing the infusion set or...
Page 33: Infusion Mode
Please confirm that the current selected brand is the same as the brand  actually used. 4.2.6 Infusion Mode Unit of Rate (ml/h)  Press to exit [Main Menu], and enter the [Rate Mode Setting/Running] interface. Mode Parameters Parameter Range Rate 0.1 - 1500ml/h Rate...
Page 34: Purge
4.2.7 Purge During infusion, the user should prevent air bubbles from entering the blood with the liquid drug, which may form an aeroembolism and put animals in serious danger. Therefore, air bubbles in the infusion set should be eliminated before the infusion. On infusion parameters setting interface, press to enter [Purge] prompt screen.
Page 35: Bolus
NOTE When in running status, if there is no operation in other interface over 2  minutes, it will return to the running screen automatically. 4.2.10 BOLUS In run screen of rate mode, press to enter [Bolus] settings screen. Follow the ways to start the bolus: Manual Bolus: Set [Bolus] rate, and then press and hold to start a...
Page 36: Complete
4.2.12 Complete When [VTBI] is not set during the infusion and infusion is completed, if drop sensor is installed and the switch of [Drip rate check] is on, the [Empty bottle] alarm will be triggered; if drop sensor is not installed, the [Air in line] alarm will be triggered. When [VTBI] is set during the infusion and the remaining infusion time is close to the [Near end] time set by the users, the [VTBI Near Done] alarm will be triggered.
Page 37 NOTE The current operating data and saved data will always be autosaved  when the device is powered off properly. The effective storage duration of the data is equal to the service life of the device.
Page 38 FOR YOUR NOTES 4-10...
Page 39: Setting Parameters
Setting Parameters 5.1 KVO KVO (Keep Vein Open) means to keep the vein open, during which the veterinary infusion pump continues infusion at a very low rate after finishing the infusion in order to prevent blood backflow or vascular occlusion. Select [Main Menu]→[KVO rate]: 0.5ml/h is unadjustable.
Page 40: Set Pressure Unit
5.2.2 Set Pressure Unit Select [Main Menu]→[Pressure unit]. Select [Pressure unit]: The 4 various forms of pressure units, mmHg, kPa, bar and psi are converted automatically, and can be selected according to actual needs. CAUTION Carefully confirm the edit when changing the current pressure unit. ...
Page 41: Acumulated Bubble
Select [Bubble size], five levels of air bubble can be selected, lowest at 50μl, and highest at 800μl. Air bubble level should be selected according to actual needs. CAUTION If the animal experiences discomfort or danger at a higher air bubble ...
Page 42: Time Near End
alarm will then alert the user to proceed to the next step. [Off] indicates closing the function. 5.7 Time Near End Select [Main Menu]→[Near end]. Select [Near end]: Off, 1-30min (when <10min, the stair-step is 1min, and when ≥10min, the stair-step is 5min). After a specific time set, when the remaining infusion time is close to the [Near end] set by the users, [VTBI Near Done] alarm will be triggered.
Page 43: View Department
5.10 View Department The veterinary infusion pump are net-connected with BeneFusion CS5 Infusion Supervision System through the approach of wireless networking, and the system contains department information, the system will automatically distribute department information to all veterinary infusion pumps when pumps are on. Select [Main Menu]→[System Maintenance]→Input User Maintenance Password “4321”→[Department] to view the department information.
Page 44 FOR YOUR NOTES...
Page 45: Other Functions
Other Functions 6.1 Nurse Call Select [Main Menu]→[System Maintenance]→Input User Maintenance Password →[Nurse call], and set in the open menu: Switch  On: indicates the opening of the nurse call function. Off: indicates the closing of the nurse call function. Signal type ...
Page 46: Wireless Networking (Optional)
NOTE Veterinarians should not consider the nurse call function as the main  alarm notice approach, and rather combine the sound and visual alarms of the veterinary infusion pump and the performances and symptoms of the animal in order to judge the animal's conditions and take further attention as needed.
Page 47: Data Export
NOTE Wireless security transmission distance is no more than 50 meters.  2.4 GHz Wi-Fi frequency range, WEP and WPA/WPA2 security modes  and 802.11b/g/n wireless standard are supported. The settings of the wireless network must be conducted by technicians ...
Page 48 FOR YOUR NOTES...
Page 49: Alarms
Alarms The alarm is used in order to alert the veterinarian by means of sound and light when abnormal situations occur during the infusion procedure which can lead to infusion changes or when the infusion of the animal cannot continue due to the unexpected breakdown or pause/delay of the veterinary infusion pump.
Page 50: Multi-Level Alarm Rules
Low-level Yellow 20 seconds Steady 100% alarms 7.2.1 Multi-level Alarm Rules When several alarms occur simultaneously, the alarms proceed according to the following rules: When several alarms at different levels occur, the visible alarms and audible  alarms are consistent with the highest-level alarms. When several alarms at different levels occur, only the highest-level alarm is ...
Page 51: Alarm Countermeasures
7.4 Alarm Countermeasures WARNING When an alarm is triggered, the animal's condition should be checked  firstly and operation should only be allowed to proceed after the reason for the triggering of the alarm is ruled out. When an alarm is triggered, please follow these steps and take appropriate action: Check the animal;...
Page 52 FOR YOUR NOTES...
Page 53: Battery
Battery WARNING The battery can not be disassembled. The battery should be changed by  maintenance staff designated by the company only. Inserting fuel cell or changing battery by personnel who has not received suitable training may cause such danger as overtemperature, fire or explode. The veterinary infusion pump is configured with rechargeable Lithium batteries to ensure that the veterinary infusion pump can be used normally under the condition of the animal's migration within the pet hospital or during the circumstance of a power...
Page 54: Battery Performance Optimization
8.1 Battery Performance Optimization When the battery is used for the first time, at least two complete optimizing cycles should be ensured. A complete optimizing cycle contains the following: Charging incessantly, and then discharging until the power of the veterinary infusion pump runs out.
Page 55: Battery Recycling
NOTE The lifespan of the battery depends on how frequently it is used and on  how long it has been used, battery capactiy decreases with increase in charging and discharging times. If the maintenance and storage of the battery is appropriate, the lifespan of the Lithium battery is no less than 300 times of full charging and discharging.
Page 56 FOR YOUR NOTES...
Page 57: Preservation And Sanitation
Preservation and Sanitation The pump must be cleaned or disinfected using the materials and methods listed in this section. The manufacturer will not be responsible for any damage or accident caused by cleaning and disinfection using other materials and methods. The manufacturer shall not be held responsible for the efficacy of the following chemicals or methods for infection control.
Page 58: Disinfection
To clean your equipment, follow these rules: Turn off the pump and disconnect the AC power source line. Wipe the display screen after soft cotton balls absorb an appropriate amount of detergent. Use a piece of soft cloth which absorbs a modest amount of cleaning agent to wipe the surface of the device.
Page 59: Maintenance
Maintenance WARNING The pet hospital or medical facility using this veterinary infusion pump  must set up a comprehensive maintenance plan. Failure to do so may result in equipment failure or other unexpected consequences, and may even jeopardize animal safety. All safety inspections or maintenance work involving the disassembly ...
Page 60: Maintenance Plan
10.2 Maintenance Plan The following tasks must be conducted by professional maintenance personnel approved by the company. Please contact the company if the following maintenances are needed. Must clean and disinfect the device before the test or maintenance. Inspection/Maintenance Items Frequency Once every two years.Perform after the Perform a safety inspection according...
Page 61: Accessories
Accessories WARNING Use the accessories specified in this chapter only. Other accessories  may cause damage to this veterinary infusion pump, or cannot reach the specification in this manual. Please do not replace an accessory if its package or itself is damaged. ...
Page 62 NOTE This Operator’s Manual describes the most complete functional  configuration of the system. The device you are using may not have some of the settings or functions described herein. 11-2...
Page 63: A Product Specifications
Product Specifications A.1 Safety Specifications A.1.1 Product Classification Classifications of this veterinary infusion pump according to the IEC60601-1 standard are as follows: Safety Components Host Type protection against electrical shock Degree of protection CF Protected against defibrillation against electrical shock Ingress Protection IP34 Explosion...
Page 64: Operating Environment
A.1.2 Operating Environment Work environment Temperature 5 - 40ºC Relative Humidity 15 - 95%, non-condensing Atmospheric pressure 57 - 106 kPa Storage environment Temperature -20 - 60 ºC Relative Humidity 10 – 95%, non-condensing Atmospheric pressure 50 –106 kPa Storage conditions Corrosive-free and ventilated indoors AC Power Supply Voltage...
Page 65: Hardware Specifications
A.3 Hardware Specifications A.3.1 Display Display Type Monochrome LCD Size (diagonal) 2.5 inches Differentiation 32 pixels A.3.2 Battery Internal battery No. of batteries 1 (standard) or 2 (optional) Battery type Lithium battery Shutdown delay At least 30 mins (new battery, after the first low battery alarm) Rated battery voltage 7.4 VDC Battery capacity...
Page 66: Auditory Indicator
A.3.4 Auditory Indicator Produce an alarm, the sound pressure is 55 - 80 dB(A) and key Speaker beep; Support multi-level volume functions; The alarm sound meets the requirements of the IEC60601-1-8 standard. A.3.5 External Ports Ports AC power supply 1 AC power supply port port 1 DB9 interface, which combines the following interface DB9 interface...
Page 67: Wi-Fi Specifications
A.4 Wi-Fi Specifications Protocol IEEE 802.11b/g/n Modulation mode CCK and OFDM Operating 2412~2484MHz frequency Channel spacing 5MHz IEEE 802.11b: 1–11 Mbps Data rate IEEE 802.11g: 6–54 Mbps IEEE 802.11n: 6.5–150 Mbps 802.11b: +18dBm(Max) Transfer power 802.11g: +16dBm(Max) 802.11n: +15dBm(Max) Operating mode STA/AP/STA+AP Data security WEP/WPA-PSK/WPA2-PSK...
Page 68 Standby time range 00:01-99:59 hh:mm Infusion mode Rate Mode KVO rate 0.5ml/h, nonadjustable Anti-bolus On, Off Low, Medium and High, respectively are 150±125 mmHg(20.0±16.7 kPa), Occl. pressure 525±125 mmHg(70.0±16.7 kPa), 900±180 mmHg(120.0±24.0 kPa). Maximum occlusion pressure is about 1300mmHg. Pressure unit mmHg, kPa, bar and psi 1 - 5, respectively are (50, 100, 250, 500, 800) μl Bubble size...
Page 69: A Reference Table Showing Occlusion Alarm Delay And Possible Dose
A.6 A Reference Table Showing Occlusion Alarm Delay and Possible Dose Occlusion Time of occlusion Rate Bolus pressure alarm (ml/h) (ml) (Level) (hh:mm:ss) 01:16:46 0.040 00:07:25 0.033 00:00:08 0.021 00:25:57 0.050 Medium 00:00:48 0.028 08:36:34 0.069 High 00:44:08 0.055 00:01:45 0.037 NOTE Test conditions:...
Page 70: Infusion Accuracy Curve And Trumpet Curve
A.7 Infusion Accuracy Curve and Trumpet Curve The following typical infusion accuracy table expresses performance after infusion has started and infusion fluctuations occurring within a certain period of time after normal infusion flow volumes have been reached. The infusion accuracy table is for reference only, detailed infusion accuracy curve is in accordance with the final device.
Page 72 Unit of Rate (Drop/min)  Sampling rate: 20 Drop/ Sampling interval: △ t =1 Test period: t =120 mins Infusion rate: Q (Drop/ min) Sampling rate: 20 Drop/ Sampling interval: △ t =1 Observation windows: p△t = 1, 2, 5, 11, 19, 31 mins Maximum deviation over course full...
Page 73: B Emc And Radio Regulatory Compliance
EMC and Radio Regulatory Compliance B.1 EMC The device meets the requirements of IEC 60601-1-2:2014. NOTE Use of accessories, transducers and cables other than those specified  or provided by the manufacturer of this device could result in increased electromagnetic emissions or decreased electromagnetic immunity of this device and result in improper operation.
Page 74 Guidance and Declaration - Electromagnetic Emissions The device is intended for use in the electromagnetic environment specified below. The customer or the user of the device should assure that it is used in such an environment. Emission test Compliance Electromagnetic environment - guidance Conducted and radiated Group 1...
Page 75 If the device is operated within the electromagnetic environment listed in Table Guidance and Declaration —Electromagnetic Immunity, the system will remain safe and provide the following essential performance: Operating mode  Accuracy  Function  Protection against UNINTENDED BOLUS volumes ...
Page 76 operation during power mains interruptions, it is 0 % U for 250/300 0 % U for 250/300 recommended that our cycle cycle product powered from an uninterruptible power supply battery. RATED power 30 A/m 30 A/m Power frequency frequency magnetic fields should 50 Hz / 60 Hz 50 Hz / 60 Hz magnetic fields...
Page 77 wireless transmitter manufacturer and d is the 28 V/m 28 V/m communication recommended separation distance 430–470 MHz, s equipment in meters (m). 800–960 MHz, IEC61000- Field strengths from fixed 1700–1990 transmitters, as determined by an MHz, 2400– electromagnetic site survey , should 2570 MHz be less than the compliance level in...
Page 78: Radio Regulatory Compliance
Recommended Separation Distances between Portable and Mobile RF, Communications Equipment and This Equipment The equipment is intended for use in an electromagnetic environment in which radiated RF disturbance are controlled. The customer or the user of the device can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the device as recommended below, according to the maximum output power of the communication equipment.
Page 79: C Default Factory Settings
Default Factory Settings This chapter presents some default factory settings.User cannot change the factory default, but may restore to the default factory settings when it is necessary. C.1 Alarms Alarm Setting Factory Default Volume Alarm sound Sound2 C.2 Interface Factory Default Brightness C.3 Parameters Setting Parameters...
Page 80: System Time
C.4 System Time System Date and Time Factory Default Time 00:00 Date 01/01/2015...
Page 81: D Alarm Information
Alarm Information This chapter presents the alarm information of the infusionpump.Prompt information for operation guidance will not be presented in this chapter. The table shows the appropriate countermeasures for each piece of information related to alarm triggering.If the problem still exists after operating according to the countermeasures, please contact the company.
Page 82 Alarm Alarm Reason Countermeasure Information level source supply is powered. automatically. veterinary infusion pump performs no operation Operate the pump or open [Reminder] during the set reminder time the door to cancel alarm. after the infusion set is loaded to it. Motor operation error, data Alarm cannot be cancelled.
Page 83 Alarm Alarm Reason Countermeasure Information level If drop sensor is installed correctly and the switch of [Drip rate check] is on, [Drop error] High current rate is ≤400ml/h, Press to cancel alarm. drop sensor detects that the drop rate deviates the preset value.
Page 84 FOR YOUR NOTES...
Page 85: E Symbols And Terms
Symbols and Terms E.1 List of Units Abbreviation Meaning ampere centigrade ℃ centimeter decibel gram hour hertz inch inch kilo kilogram kilopascal litre pound meter milligrams minute milliliter millimeters mmHg millimeters of mercury second μg Microgram volt volt ampere watt...
Page 86: List Of Symbols
E.2 List of Symbols Symbols Meaning minus percent Per; divide; or ～ power plus ＋ equal to ＝ < less than > greater than ≤ less than or equal to ≥ greater than or equal to plus or minus ± ×...
Page 87 Abbreviation Meaning European Economic Community Electromagnetic compatibility Electromagnetic interference C2H4O Intensive Care Unit Identification International Electrotechnical Commission IEEE Institute of Electrical and Electronic Engineers International organization for Standardization Keep vein open light emitting diode Maximum Medical Device Directive Minimum magnetic resonance imaging not applied NICU Newborn Intensive Care Unit...
Page 88: List Of Unit Conversion
E.4 List of Unit Conversion Unit Symbols Unit Conversion 1kPa=7.5mmHg=0.145psi=0.01bar 1psi=51.724mmHg=6.897kPa=0.069bar 1bar=750mmHg=14.5psi=100kPa 1 lb=0.454kg drop/min drop/min = (ml/h×drip)/60...
Page 89: F Toxic And Hazardous Substances Or Elements
Toxic and Hazardous Substances or Elements Cr(VI) PBDE Name of the Parts Cr(VI) PBDE ○ ○ ○ ○ ○ ○ Front housing ○ ○ ○ ○ ○ ○ Back housing Device ○ ○ ○ ○ ○ ○ Keys housing ○ ○...
Page 90 FOR YOUR NOTES...
Page 91 P/N: 046-00035A-00(2.0)
Page 92 GERMANY SWITZERLAND POLAND EICKEMEYER KG EICKEMEYER AG EICKEMEYER Sp. z o.o. Eltastraße 8 Sandgrube 29 Al. Jana Pawła II 27 78532 Tuttlingen 9050 Appenzell 00-867 Warszawa T +49 7461 96 580 0 T +41 71 788 23 13 T +48 22 185 55 76...

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