HELP WITH SAFETY CARE For every type of use, Hillrom™ beds provide patients with optimal comfort and greater independence for a feeling of well-being that is conducive to a swift recovery. They are also easy to use for caregivers. 194412(11) - Hill-Rom® 900 Accella™ Bed - Instructions For Use...
Symbol definitions This Instructions for Use contains different typefaces and icons designed to improve readability and increase understanding of its content. Note the following examples: • standard text - normal character style used for “basic” information. • Boldface text- emphasizes a word or phrase. ...
Bed model and country of use Certain features or accessories may be available or not, depending on the destination country. These features are identified with an asterisk (*) and the accessories or the additional parts are identified by two asterisks (**). To identify your bed model, its serial number SN (HRPXXXXXXXXX),its UDI and its date of manufacture, refer to the identification label (see “Overview”...
Safety and Usage Tips Intended Use The Hill-Rom® 900 Accella™ LI900B4 medical beds, with CPR, are intended for intensive (the CPR function remains operational in the event of an electric power outage), acute and ambulatory care for adult patients (EN60601-2-52 application environments 1, 2 and 5).
Training can be provided on demand. Caregivers must be informed of the risks that may be encountered in the use of electric beds. The many sources and types of accessories, hardware, or medical devices that may be used together with this bed do not enable Hill-Rom to guarantee both the safety and conformity of all the combinations thus created.
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• always check (e.g. to and fro movements) that the various locking mechanisms are in good working order (e.g. siderails, extensions, brakes). • sufficiently qualified nursing staff determines the usage condition suitable for the various functions and the degree of supervision to ensure that the patient uses the bed safely.
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One measure which has already proved effective is to draw up a protocol specifying: situations and conditions for siderail use and authorized mattress type or model, for all patient monitoring procedures, both for restrained and unrestrained patients, including during intervals, circumstances under which patients must be restrained according to the instructions and recommendations of the manufacturer of the said restraining devices.
Recommendations for the function lockouts The electrical function management control prevents any unintended bed movements that might cause injury to the patient. It is highly recommended that functional lock out should be used whenever a patient is undergoing examination or treatment or when the bed is being serviced or moved.
Use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in improper operation. If such use is necessary, this equipment and the other equipment should be observed to verify that they are operating normally.
Climatic restrictions Service temperature +10° to +40° C Service humidity 30% - 85% Working atmospheric pressure 700 hPa to 1,060 hPa Precautions for transport and storage The following conditions must be met to ensure that the bed and its accessories are shipped and stored in complete safety.
Technical specifications Hill-Rom has an ongoing continuous improvement policy. Therefore specifications are liable to be altered without notice. 28° 65° -22° Features Value Maximum width (W) 995 mm Maximum length (without extension) (L) 2158 mm Maximum length (with extension closed) (L) 2158 mm Maximum length (with extension open) (L+) 2358 mm...
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Features Value Chassis clearance (double-band 125 diameter casters) (C) 150 mm Chassis clearance (double band 150 diameter casters) (C) 195 mm Chassis clearance (150 diameter casters) (C) 203 mm Head section incline + 65° Thigh section incline + 28° Foot section incline - 3°...
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Characteristics of the weigh system (scale) The weigh system of the Hill-Rom® 900 Accella™ bed uses four weighing cells installed in the bearing structure of the bed. The bed is made up of a mobile structure (the weigh system) and a fixed structure (the frame). Features Value Class III...
Overview Name Item Item Name Half-siderails Extension + linen holder* Headboard Bumper (4) 2 sockets for I.V. pole and patient Central brake and steer bar helper control Caregiver half-siderail controls 150 mm diameter casters Head section “CPR” control Bilateral HiLow pedal with caregiver mode* Patient half-siderail controls Control pendant*...
General Symbols Manufacturer Date of manufacture Product reference Serial number General safety sign Equipotential terminal Refer to the Instructions Type B Equipment for Use. DO NOT BIN, follow the local recycling Direct current regulations. Danger – Do not use Alternating current Earth leakage circuit Recyclable material breaker rating...
Do not store in the place No oxygen tents shown Medical Device Medical Device conformity mark conformity mark Bed with a weigh system NF MEDICAL - LITS compliant with Directive compliant 2014/31/EEC NF ENVIRONMENT Steam cleaning compliant bed Compliant with the Compliant with the ROHS Europe ROHS China regulations...
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References of recommended Patient helper position mattresses Information page 36 Information page 22 Caster control Footboard lock label Information page 28 Information page 81 Earth continuity and earth leakage current Unweighed support indicator label Metrological certification label of the In service inspection label weigh system 194412(11) - Hill-Rom®...
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Electrical controls Bilateral HiLow pedal with caregiver mode* Lock control under the pedal* (for use by caregivers only) Caregiver half-siderail control Bed not in lowered position indicator Nurse call activator Battery charge 45° indicator light Fault indicator light. Service required Indicator light message on CGI™.
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Graphical Caregiver Interface (GCI)™ controls Active therapeutic active* Bed* exit alerts mode MCM* Backrest (Head) angle Home alert Access to Scale* Access to the Bed exit Suspend alerts Mode Duration Access to the combined alert Accella™ Therapy mattress* Access to the Angle of the Parameters adjustable head...
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Page 20 194412(11) - Hill-Rom® 900 Accella™ Bed - Instructions For Use...
Installing the patient Before placing the patient on the bed Assess the various risks, including but not limited to the following (incomplete list): • Make sure that all the moving parts are in good working order. • risk of entrapment, •...
Using accessories and peripheral equipments other than those recommended by Hill-Rom may incur risks of damage or accidents to users. Mattress** For the Hill-Rom® 900 Accella™ bed, Hill-Rom recommends the Hillrom™ mattresses listed below, which are compatible with the safety recommendations (see “Risk prevention” page 5):...
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Adjustable mattress clamp The position of the clamps must be adjusted according to the width of the mattress in order to center and secure the mattress. To avoid creating entrapment zones, make sure that the mattress is centered and secured on the sleep surface by the folding clamp at the foot of the bed, with the adjustable clamps in the L or S position.
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References of recommended mattresses 90 cm wide mattresses are incompatible with egress handles*. Clamp Part number Name position P02033A Primo™ mattress AD085A (200 x 85 x 16 cm) ClinActiv® Alternating Low Pressure mattress system AD237A P02062B (230V) (203 x 85 x 18 cm) ClinActiv®...
Clamp Part number Name position P006173A P280 Air Mattress (120V) (198 x 85x 17 cm) FHS01C0XX Fusion Hybrid mattress (197 x 88 x 17 cm) P290A1 P290 Air overlay mattress (200 x 90 x 10 cm) P290A2 P290 foam base mattress + Air overlay (200 x 90 x 17 cm) P290A3 P290 Air mattress (200 x 90 x 17 cm) ASS078...
Endboards Non-locking head endboard Lockable foot endboard Installing the endboards Headboard The headboard is fitted with fins that must point towards the sleep surface. If the headboard is installed in the bed frame the wrong way round, the risk of entrapment increases.
Footboard fastening system System locked System unlocked System locked Bed frame extension* Do not sit or climb on the extension The extension can be pulled out by 20 cm in intermediate steps of 4 cm. Cushion for extensions is available as an additional mattress. Part number Name ASS078...
Mobilizing the patient Electrical Functions Controls The bed’s power-driven movements are controlled using the controls built into the half- siderails or bilateral HiLow pedals* with caregiver mode* or the control pendant* by pressing and holding the button for the corresponding function. The movement stops when the button is released or when the limit of movement is reached.
Bilateral HiLow pedal with caregiver mode* The HiLow pedals are positioned on each side on the chassis. They are to be used by caregivers. Raising/lowering the sleep surface Before using this function, check that no obstacles (e.g., objects, accessories, power cables) or persons (especially children) are under the sleep surface and that none of the patient’s limbs protrude beyond the edges of the sleep surface.
The HiLow lock out on the controls built into the half-siderails does not lock out the HiLow pedal, which remains operational. By default, the pedal is locked to avoid accidental movement. It is necessary to unlock the HiLow pedal before use. ...
Electric AutoContour™ The AutoContour™ is available when both the adjustable head section and the adjustable thigh section functions are enabled.. The AutoContour™ simultaneously raises the head section and the thigh section. This function prevents patients from slipping. Trendelenburg/Reverse Trendelenburg The sleep surface can be titled in two ways: •...
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Before using this function, check that: • the bed frame extension is securely locked in one of the notches and that nothing (e.g., objects, accessories, power cables, tubes) or persons (especially children) are under the sleep surface. • the patient’s limbs are within the sleep surface, •...
Chair position The chair position gradually returns the patient to the vertical position without having to leave the bed. Place sleep surface flat This function flattens the sleep surface and descends the bed into the lowered position by pressing a single button. Bed exit aid This function makes it easier for the patient to get out of the bed by raising the head section to up to 45°, flattening the thigh section and lowering the sleep surface to the...
Mechanical adjustable foot section The foot section can be placed in four different positions and is held in place by mechanical notches. To raise the foot section: CLICK To lower the foot section: CLICK Patient helpers** This accessory must only be fitted at the head of the bed. Fixed patient helper - AD810A Safe working load: 75 kg Do not position the patient helper at the outside of the bed.
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Adjustable patient helper - AD811A Safe working load: 75 kg The adjustable patient helper can be placed in three positions. Patient Helper Positioning The patient helper in the patient transfer position is designed to help the patient lift some of his/her weight so as to assist the nursing staff with their work. This position is not designed to allow patients to transfer themselves alone.
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Patient helper handle The patient helper handle must be positioned between lugs A and B to avoid any danger of slippage. The patient handle on the patient helper can be adjusted to the patient. Adjust the height of the handle until there is a right angle at the elbow.
Graphical Caregiver Interface (GCI)™ controls The GCI is on the foot siderail. To activate the GCI: • Touch the screen. • To release, press the round symbol until the green light above it comes on, then PRESS FIRMLY and slide your finger to the right so that the remaining LEDs come on.
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This information can be sent to the duty nurse if the bed is connected to a hospital network with a compatible information system.(see “Sending bed exit alerts*” page 40) The patient position monitor system does not remove the need to secure the patient in the bed (see “Risk prevention”...
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Press Alerts on the GCI. Wait for the selection screen to open. Activation is confirmed by a beep. NOTE: If the pre-conditions for activation are not met, an error message appears. In this case, follow the instructions and repeat the procedure. Select one or more modes from: •...
Backrest (Head) angle alert The Backrest (Head) angle alert allows the caregiver to program a sound alert when the angle of the head section is less than 30° or 45°. A message appears on the GCI when the head section descends below the selected angle. ...
Alert suspension mode When a detection function is activated, it can be suspended using the Suspend Alert for 30 sec command on the home screen, then suspended again for 5 to 10 minutes, without having to deactivate the detection function. To activate the alert suspension mode Select Suspend Alert for 30 sec on the touch screen.
“Awaiting patient” mode In this mode, the Bed exit alerts (Bed exit alerts) are deactivated until the patient returns. IThe monitoring system can be completely deactivated by pressing Disarm. When the patient returns to the bed, the system reactivates the alerts. NOTE: If the system is unable to reactivate itself after a given length of time, the Bed exit alert sounds.
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Preparing the bed for a reset/tare operation* or initializing the Bed Exit alerts system* Ensure the bed is on a flat surface and that the frame is horizontal (+/-2°). Check that the transport chock protecting the weigh system have been removed from their housing.
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Check that neither the mattress nor any accessories are touching the fixed parts of the bed (and in particular the head section) and that no traction is applied to the parts installed above and below the sleep surface (e.g., power cable and air mattress pipes).
Weigh the patient The weigh system is used to obtain the weight and BMI of the patient. This information must never be used alone for therapeutic purposes or to monitor the patient's vital parameters. Make sure that the patient is lying in the center of the bed.
Display the weight to within 100 g Press Scale on the GCI. Press the command 100g Magnification The weight is displayed to within 100 g for 5 seconds. Add/remove parts on the bed Caregivers can use this function to change the parts on the bed without changing the weight reading on display.
combined Accella™ Therapy mattress* The Accella™ Therapy is a therapeutic mattress. It has two operating modes: continuous low pressure (CLP) and alternating low pressure (ALP), with permanent regulation by the I-mmersion™ sensor in both modes. This device is intended for patients weighing between 40 and 185-215 kg, depending on the environment, and offers therapeutic benefits up to 160 kg.
Connect the plug to the bed connector (it clicks into place). Install the hard surface of the thigh section. Attach the mattress to the middle section of the frame with the straps. 10. Adjust the length of the straps. 11. Unfold the mattress. 12.
Therapeutic mode Continuous low pressure (CLP) mode Press CLP to select this mode. The corresponding control turns green. The patient is supported at an optimal low pressure controlled by the I-mmersion™ sensor. Alternating low pressure (ALP) mode Press ALP to select this mode.. The corresponding control turns green.
Pressing the CPR button on the caregiver keypads or pressing the handle on the adjustable head section activates the CPR function. The mattress deflates in approximately 30 seconds. Press Rearm Matress to restore normal operation of the mattress. The mattress CPR function only works if the mattress is active and its battery is fully charged (it takes 24 hours to charge the battery).
Stopping the mattress To stop the mattress: Press Mattress du GCI. Press Stop. The mattress deflates in about 1 minute. A sound signal indicates that the mattress can be disconnected. Confirm that the mattress has been stopped. NOTE: If the mattress is disconnected without properly following the procedure to stop the mattress, it switches to fault mode.
Settings Choosing the language Your bed is configured for the destination country. In this menu, you can set the language of the GCI. Press Parameters on the GCI. Press Settings. Press Language and select the language. Press Close to confirm. Setting the date and time ...
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Yes or No. Press Save to confirm your choices. NOTE: The “Manual Locating” and “Patient Id Display” functions are only valid for the Hillrom™ Digital Health Gateway. Latitude/altitude information This menu is used to access the latitude and altitude information.
• Adjustable head section angle alert • Last scales function used • Bed exit alerts • Bed battery charge level a. by SmartSync™. b. by Hillrom™ Digital Health Gateway. 194412(11) - Hill-Rom® 900 Accella™ Bed - Instructions For Use Page 55...
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Bed located and patient identified If the bed switches to battery mode, it is no longer assigned, but remains paired for 3 minutes (SmartCare™) or 1 minute (Hillrom™ Digital Health Gateway). After this time, it is necessary to proceed with a new assignment.
Follow the information system supplier’s instructions to pair and couple the bed. NaviCare® system* NaviCare® is a system used to connect and check Hillrom™ beds and mattresses. It sends alerts to caregivers. Refer to the NaviCare® system Instructions for Use for more detailed information about the use of this system.
Wi-Fi Connection Module (WCM) - AD315A** ON/OFF Button ON/OFF Wi-Fi Server Connection Bed Location Light Light Light Light Identification To identify your MCW AD315A model, its serial number SN (XXSEXXXXXX) and its date of manufacture, refer to the identification label on the back of the module. •...
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Bed Location: The Bed Location light turns green. NOTE: The bed is located automatically if it is connected to SmartSync™, and manually if it is connected to the Hillrom™ Digital Health Gateway. The bed can then transmit the information to the facility communication system and the bed is located and associated with the room.
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Bed-locating procedure Check that the “manual location” mode is active (see “Setting the Wi-Fi options” page 54). Only applies to the Hillrom™ Digital Health Gateway. The Wi-Fi is not active: Press the button to switch on the Wi-Fi connection.
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Check that the “Patient Id Display” mode is active (see “Setting the Wi-Fi options” page 54). Only applies to the Hillrom™ Digital Health Gateway. This procedure is only possible if the following three conditions are met: the bed has been located, the server proposes a patient name for this room and the patient is in the bed.
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If the patient identity is correct, confirm by pressing Yes. The date of birth is always displayed or is only provided when the identity is confirmed for the first time, if the “Patient Name Encoding” function is active (see “Setting the Wi-Fi options” page 54). The patient identity is then associated with the bed.
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Management of Wi-Fi connection profiles Press Parameters on the GCI. Press Technician Access. Enter the code 9004 and confirm by pressing OK. Press Wifi Profile Management. Check that the Wi-Fi is active. Activate if necessary. There are two configuration modes: Scan and Manual.
Configuration in “Manual” mode Press New Profile. Enter the parameters in the same way as for Scan mode. Press Save to save the settings. Activating a profile Select a profile from the list (e.g., PROFILE NAME The profile turns green. The profile is active.
Patient safety Siderails The Hill-Rom® 900 Accella™ Bed is fitted with built-in half-siderails. Always ensure that there are no obstacles (patient's limb, objects, accessories, etc.) before raising, lowering folding or unfolding a siderail. They are not designed to restrain or immobilize the patient. Restraining straps or other devices must not be fastened to the siderails.
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Raising a half siderail CLICK Lowering a half siderail Half-siderail position indicator* The half-siderails can be equipped with sensors to indicate the raised or lowered position. This information can be sent to the duty nurse if the bed is connected to a hospital network with a compatible information system.
Space filler panel (AD288A)** In order to mitigate the risks incurred by patient egress through the gaps at the foot of the bed, between the half-siderails and the foot panel, Hill-Rom has developed a kit of two detachable panels, one for each side, designed to block this gap. Installing the panels 194412(11) - Hill-Rom®...
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The panels are not designed to restrain or immobilize the patient in the bed. Check that the panels are correctly installed. The authorized medical personnel must consider the use of siderails depending on the state of health and behavior of the patient, according to a protocol that indicates in which situations and when the panels can be used.
Fittings for the restraining strap handles Do not attach the restraining straps to any part of the bed (particularly the siderails) other than those provided for this purpose. When the patient is restrained by the straps, the electric functions must be locked out. When the patient is restrained with an abdominal strap, a system used to restrict the ankles must also be used.
Restraining devices must not be used as a replacement for the nursing care required by the patient. Even when correctly installed, physical restraining devices may become entangled and injure the patient, especially if the patient is agitated and confused. Whenever containment devices are used, the patient must be observed in accordance with legal requirements and protocol.
Bed not in lowered position indicator A light on the caregiver keypads on the two half-siderails goes off when the bed is in the lowered position. This position is recommended when patients are left unattended. This information can be sent to the duty nurse if the bed is connected to a hospital network with a compatible information system.
Never allow a non-qualified person to operate this function and check that no obstacles (e.g., limbs, accessories, objects, power cords) or persons are under the head section. This function is used in emergencies (e.g., reanimation, heart massage, etc.) or in the event of a power failure.
Equipotential terminal Failure to connect the equipotential cable may result in corporal injury. When direct intravascular or intracardiac connections are in use, the electric potentials of all the unprotected metal parts need to be equalized. The bed must be connected to the electrical installation. To equalize potentials if a grounded power connection is unavailable, connect the equipotential cable (AC968A) to the connection terminal on the bed and the device.
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Page 74 194412(11) - Hill-Rom® 900 Accella™ Bed - Instructions For Use...
Help with care Fixed IV pole (AD294A)** The IV pole is mounted in the angle supports and is used to hold IV bags. Safe working load: Refer to the value indicated on the IV pole Telescopic IV pole (AD298A-AD299A)** The IV pole is mounted in the angle supports and is used to hold IV bags.
Using the IV pole (AD299A)** To adjust the height or angle of the IV pole: Linen holder* The linen holder must not be used to support luggage or as a seat, even for young children. Do not sit or climb on the linen holder Safe working load: 15 kg 1.
Drainage bag holder pins The urine bags attached to my pins will not be taken into account in weighing. Oxygen cylinder holder (AC959A-AD101A-AD102A)** Safe working load: 15 kg The oxygen cylinder holder is designed to accept an oxygen cylinder and must only be fitted on the patient helper supports at the head end of the bed outside the sleep surface.
The following recommendations are designed to prevent any possible incidents so that this accessory can be used in optimum safety conditions for both the patient and nursing staff. • Check that the cylinder is correctly positioned at the base of the cylinder holder.
Monitor stand (AD244B)** Safe working load: 15 kg The monitor stand fits into the sockets at the foot of the bed. When fitting the monitor, ensure that the folded table is located on the outer edge of the bed. The table must be folded away when ...
Syringe-driver holder (AC963A)** Safe working load: 15 kg Do not position the accessory facing inwards, particularly under the head section when it is raised, so as to prevent any risk of the accessory obstructing the head section or siderail when being handled. This accessory is designed to accept a syringe-driver and is fitted at the head end of the bed in the sockets provided.
IV line manager & support (AD286A)** This accessory must be fitted by an authorized technician. Please refer to the fitting instructions provided with the accessory when fitting the accessory. A Line Manager is on each side of the head end of the bed. The Line Manager helps to keep lines (such as IV lines, suction lines, etc.) togetherand away from the articulating frame.
X-ray-transparent adjustable head section (AD242A)** The X-ray-transparent adjustable head section accessory allows a cassette for 35 x 43 cm X-ray films (as per the standard EN ISO 4090) to be installed in order to take chest X- rays. It is installed in place of the hard surface of the head section. ...
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Lift the cassette retaining bar and insert the cassette in the landscape or portrait direction, as required. Check that the retaining bar locks the cassette in position. For portrait images, pull the retaining bar upwards to lock the cassette. If necessary, adjust the cassette in the sideways direction. Adjust the position of the cassette using the right and left straps so that the retaining bar is positioned on the edge of the mattress.
13. Adjust the position of the cassette as required. Removing the X-ray cassette Pull on the left strap to extract the cassette support. Raise the retaining bar and take out the cassette. Pull on the right strap to insert the cassette support. Hook the buckle of the right strap on its storage hook.
Movements/Transfers Brake and steer system Brake and steer system Always put the brake in the “STOP” position, except during transport. Once the brakes have been applied, push and pull the bed to make sure that it does not move. The brake bar, located at the foot of the bed, or the bilateral pedals at the head end, simultaneously control all four casters, including one steering caster.
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Using the bar in the steering position wheel (basic version): • without 5 All four wheels turn freely (NEUTRAL) and one wheel steers (it no longer swivels). Steering wheel at head end Steering wheel at foot end* • with 5 wheel with controlled release*: When the brake and steer bar is in the steering position, the 5 wheel...
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"Bed connected to power mains, brake not applied" detection* When the bed is plugged into the mains and the brakes are not applied, a continuous alert sounds until the brakes are applied or the bed is disconnected from the mains. ...
After moving • Apply the brakes, • connect the bed and accessory power cords, • connect the nurse call system communications cable. Securing the power cable Always correctly store the power cable. Failure to follow this recommendation may result in damage to the cable by crushing and create the risk of electric shock. The power cable must be hooked in place before moving the bed.
Decontamination, Maintenance Decontaminating the bed Safety Recommendations • Ensure that the bed cannot move. • Lock out all electrical functions. • Disconnect the bed and stow the power cable (see “Securing the power cable” page 84). • Check that all plugs are well connected (control unit, electric motors on the power supply unit).
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Recommended cleaning and disinfection Clean and disinfect every day. Clean and disinfect after patient departure or before patient transfer. Clean and disinfect thoroughly (after the departure of an infected patient or recommended every two months). Decontamination Record A decontamination record should be kept for each bed, mentioning: •...
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Recommended Materials and Products NOTE: A list of recommended cleaning products for all types of cleaning requirements is available on your request along with a special maintenance advice leaflet. • Single-use tissues or recyclable textile wipers. • One pair of household gloves. •...
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Steam Cleaning These beds can be steam cleaned. However, in order to avoid any damage or deterioration caused by high pressure or abnormal surface temperature, the following precautions should be taken: • avoid any excess water and use reduced steam pressure with microfiber support when cleaning electrical components (control unit, actuators, lateral caregiver units, half-siderails with keypads, remote controls and control cluster arms),...
Servicing the bed Safety recommendations Only facility-authorized personnel should perform maintenance of the Hill- Rom® 900 Accella™ bed. Before maintenance or servicing works: • ensure that the bed has been immobilized (if no movements are required), • lock out all electrical functions, •...
• earthing of the metal parts of the bed, • waterproofing of electrical parts, • protection of the (CAN) connector outside maintenance operation, • siderails: check the play and the lock mechanisms (condition and working order), • weigh system and bed exit alerts system: frequency regarding national regulations.
Description: LITHIUM BATTERY 3V CR2032 Part Number: CR2032MFR Manufacturer: RENATA BATTERIES U.S. 1,2-dimethoxyethane; ethylene glycol dimethyl Substance Identification: ether (EGDME) Substance Concentration: 1-3.5% by part weight Inside the battery Substance Location: For electronic devices with data storage that can still have treatment and patient data on them, this data should be deleted before disposal of the device, as a matter of cybersecurity procedure The bed is designed for easy dismantling so that it can be destroyed or reused in...
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Page 96 194412(11) - Hill-Rom® 900 Accella™ Bed - Instructions For Use...
Appendix Warranty and after sales service conditions The warranty for our beds will be rendered null and void, in part or in total, in the event of: • unauthorized interference with or incorrect maintenance of: • actuators, • electrical drives and components, •...
• The Hill-Rom® 900 Accella™ bed meets the "NF Environnement - Ameublement" - Institut Technologique FCBA 10, rue Galilée 77420 Champs-sur-Marne FRANCE www.fcba.fr - The NF ENVIRONNEMENT marking guarantees performance and ecology: •Quality / Durability •Health / Safety •Environment Visit the website for more information www.nf-environnement-ameublement.com •...
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The Hill-Rom® 900 Accella™ bed must not be used close to or on top of other items of equipment. If this is necessary, the Hill-Rom® 900 Accella™ bed must be tested to confirm that it functions properly in the required configuration. Make sure that the Hill-Rom®...
Compliance with electromagnetic immunity Manufacturer's guide and declaration – electromagnetic immunity The Hill-Rom® 900 Accella™ bed and the Wi-Fi connectivity module are designed for use in the electromagnetic environment specified below. Users must ensure that they are used in this environment.
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Manufacturer's guide and declaration – electromagnetic immunity The Hill-Rom® 900 Accella™ bed and the Wi-Fi connectivity module are designed for use in the electromagnetic environment specified below. Users must ensure that they are used in this environment. Immunity test IEC 60601 Compliance Electromagnetic environment - Guide Severity...
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IMMUNITY to Proximity Fields from Radio Frequency Wireless Communications Equipment In addition to the Radiated RF IEC 61000-4-3 as shown in the table above, the Wi- Fi connectivity module has been tested as specified in the table below. 380 - 390 TETRA 400 Pulse modulation 18 Hz...
Recommended separation distances Recommended separation distances between portable and mobile RF communications equipment and the Hill-Rom® 900 Accella™ bed and the Wi-Fi connectivity module. The Hill-Rom® 900 Accella™ bed and the Wi-Fi connectivity module are designed for use in an electromagnetic environment in which interference due to radiated RF is monitored. The user of the Hill-Rom®...
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Regulatory Information Changes and/or modifications not expressly approved by Hill-Rom Co., Inc. could void the user's authority to operate the equipment. The module must be installed and used in accordance with the Hill-Rom user and installation instructions. Hill-Rom is not responsible for any radio or television interference caused by unauthorized modification of the devices included with the Hill-Rom module, or the substitution or attachment of connection cables and equipment other than that specified by Hill-Rom Co., Inc.
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equipment off and on), the user is encouraged to take one of these measures to try to correct the interference: • Move this device. • Increase the separation between the device and the receiver. • Connect the device to an outlet on a circuit different from that of other electronics.
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DECLARATION UE DE CONFORMITE Directive RED 2014/53/UE DECLARATION UE OF CONFORMITY SOCIETE (fabricant ou mandataire) Hill-Rom S.A.S. COMPANY (manufacturer or authorised representative): Nom : Hill-Rom S.A.S. Name: Hill-Rom S.A.S. Adresse : Z.I. du Talhouët, 56330 PLUVIGNER, FRANCE Address: Z.I. du Talhouët, 56330 PLUVIGNER, FRANCE La présente déclaration de conformité...
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DECLARATION UE DE CONFORMITE Directive RED 2014/53/UE DECLARATION UE OF CONFORMITY SOCIETE (fabricant ou mandataire) Hill-Rom COMPANY (manufacturer or authorised representative): Hill-Rom Nom : Hill-Rom S.A.S. LI900B4 Name: Hill-Rom S.A.S. Adresse : Z.I. du Talhouët, 56330 PLUVIGNER, FRANCE Address: Z.I. du Talhouët, 56330 PLUVIGNER, FRANCE La présente déclaration de conformité...
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