Hausted 5E82 Electric Surgi Stretcher User Manual

ELECTRIC SURGI-STRETCHER
5E82EYEST, 5E82EYXST, 5B800ST
ELECTRIC SURGI-STRETCHER WITH
NAVIGATOR SMARTDRIVE SYSTEM
5E82EYEST-PD, 5E82EYXST-PD, 5B800ST-PD
OPERATING MANUAL

SAVE THIS MANUAL FOR FUTURE USE.

INTRODUCTION — A WORD FROM GF HEALTH PRODUCTS, INC.

This manual contains important information on proper use and maintenance of the Hausted® Series 5E82 / 5B8 Surgi-Stretchers. All personnel involved in the use and maintenance of this equipment must carefully review and comply with the warnings, cautions and instructions contained in this manual. These instructions are important to protect the health and safety of personnel operating these models and should be retained in a conveniently accessible area for
quick reference.
Complete instructions for uncrating and putting your new equipment in service, as well as equipment drawings, have been furnished. If missing, contact GF Health Products, Inc. (“GF”) for replacement copies, giving the serial number and model number of the unit.
GF Health Products, Inc. carries a complete line of accessories for use with these stretchers; your representative will gladly review these with you.

Indications for Use
The Hausted Surgi-Stretchers are intended for a healthcare professional to use in patient treatment, transport, or recovery. This product has an expected service life of five years.
The articulating head piece with dual operating control knobs allows adjustability and precise movement of the head section. Patient positioning is convenient and easy for both care provider and patient with the electric/battery powered controls for adjustment of height, backrest and knee flex.
To ensure the basic safety of the patient, the stretcher is designed, tested, and evaluated to IEC Standard 60601-1 and in accordance with IEC 60601-2-46 wherein the essential performance in any single fault or combined fault condition is no unwanted movement of the stretcher when in use. See also page 7 Electromagnetic Compatibility (EMC) information. The stretcher is tested and certified to IEC 60601-1-2 (Ed. 4) for EMC.

Service Information
A thorough preventive maintenance program is essential to safe and proper unit operation. This manual contains maintenance schedules and procedures which should be followed for satisfactory equipment performance.
We encourage you to contact GF Health Products, Inc. with maintenance concerns.

Advisory
A listing of the safety precautions to be observed when operating and servicing this equipment can be found in Section 1 of this manual. Do not operate or service the equipment until you have become familiar with this information. Any alteration of this equipment not authorized or performed by GF Health Products, Inc., could affect its operation, will void the warranty, could violate national, state, and local regulations, and could jeopardize your insurance coverage.

Info: Column 1 below applies only if product was purchased outside the U.S.

EC Authorized Representative:
CEpartner4U BV
ESDOORNLAAN 13
3951DB MAARN
The Netherlands
+31(0)6 516 536 26| Manufactured by:
GF Health Products, Inc.
One Graham-Field Way
Atlanta GA 30340-3140
1.770.368.4700 Main
1.770.368.2386 Fax
www.grahamfield.com
www.Hausted.com| Class 1 Equipment
Type B Equipment Equipment not suitable for use in the presence of flammable anesthetic mixture with air or
oxygen or nitrous oxide.
IPX4 Not suitable for continuous operation (Duty Cycle:
10% 2 Min. in 18 Min.)
---|---|---

Info: The base language of this document is ENGLISH. Any translations must be made from the base language document.

LIST OF WARNINGS AND CAUTIONS

IMPORTANT: Before using the Surgi-Stretcher, please read and adhere to the following safety precautions and warnings. Failure to do so could result in serious personal injury or damage to the Stretcher.

Always consult your healthcare professional to determine safe methods most suitable for your individual abilities. Protect yourself, your attendant, and the Surgi-Stretcher by having it serviced regularly. If you experience any malfunction, contact your Graham-Field authorized distributor immediately, as a hazardous condition could result, causing personal injury or damage to the Stretcher.
Periodic inspection, adjustment and replacement of worn parts are necessary to provide years of excellent service. Maintenance MUST be performed by qualified personnel ONLY.

SAVE THESE INSTRUCTIONS.
SIGNIFICANCE OF SAFETY STATEMENTS

Please note the following special statements, used throughout this manual, and their significance:
DANGER: Indicates a potential hazard situation or unsafe practice that, if not avoided, will result in death or serious personal injury.
WARNING: Indicates a potential hazard situation or unsafe practice that, if not avoided, could result in death or serious personal injury.
CAUTION: Indicates a potential hazard situation or unsafe practice that, if not avoided, could result in minor or moderate personal injury.
NOTICE: Indicates a potential hazard situation or unsafe practice that, if not avoided, could result in product or property damage.

Info: Provides application recommendations or other useful information to ensure that you get the most from your product.

DANGER / WARNING / CAUTION / NOTICE Summary
The following is a listing of the safety precautions which must be observed when operating and servicing this equipment. These precautions are repeated (in whole or in part), where applicable, throughout the manual.
DANGER: To Reduce the Risk of Burns, Fire, or Electric Shock
DANGER: SHOCK HAZARD — To reduce the risk of electric shock, unit is to be serviced by qualified personnel only.
DANGER: SHOCK HAZARD — To avoid the risk of electric shock, this equipment must only be connected to supply mains with protective earth.
WARNING: To Reduce the Risk of Personal Injury
WARNING: LACERATION HAZARD — When cutting bands always use a tool specifically designed for that purpose.
This will help to avoid personal injuries frequently incurred when bands are cut and tension released.
WARNING: Do not sit on end — tipping may occur.
WARNING: Ensure IV rod is inserted completely into socket up to the arrow before applying load.

WARNING — CAUTIONS AND PROPER OPERATION
WARNING: The Series 5E82 / 5B800 stretchers have a maximum patient weight capacity of 800 lb (363 kg), EVENLY DISTRIBUTED.
WARNING: The Series 5E82 / 5B800 stretchers have a maximum weight, including equipment weight, and patient weight of 1200 lb (544 kg), EVENLY DISTRIBUTED.
WARNING: Patient entry, egress and transfer should always be performed with the brakes locked.
WARNING: The patient transport position is pushing from the patient head end in the supine position.
WARNING: The brakes should always be locked and patient side rails up when patient is not in transport.
WARNING: Clip patient pendant to rail when not in use – keep cord clear of moving parts.
WARNING: All electric powered stretchers are equipped with a built-in battery backup system, but the unit should remain plugged into wall receptacle during normal use.
The battery backup is intended for transport and EMERGENCY only.
WARNING: The stretcher has a warning label on both the head and foot end stating: “Do not sit on end – as tipping may occur.”
WARNING: Patient entry, egress, and transfer from the stretcher should always be from the center side rail location with the side rail in the down position and brakes locked.
WARNING: The back quick drop handle is intended to be used during emergency situations only.
WARNING: To turn on electric controls, plug into wall receptacle. To turn off, remove plug from wall receptacle. Electric powered stretchers do not have a separate on / off switch.
WARNING: Always disconnect the power source whenever troubleshooting or servicing any electric powered stretcher.
WARNING: Cables can become pinched. Keep cables away from column.
WARNING: Steam cleaning and pressure washing of chair is not recommended and can void warranty.
WARNING: Do not modify the equipment without the authorization of the manufacturer.
WARNING: When lowering the rails, ensure patient and caregiver body and extremities are clear of pinch points before operating the rail.
WARNING: Keep hands clear of pinch points.
WARNING: Stow away power cord when not in use to prevent injury or damage.

ELECTROMAGNETIC COMPATIBILITY (EMC) INFORMATION
WARNING: Medical Electrical Equipment needs special precautions regarding EMC and needs to be installed and put into service according to the EMC information provided in this manual.
WARNING: Electronic equipment may be influenced by Radio Frequency (RFI). Caution should be exercised with regard to the use of portable communications in the area around such equipment. Portable RF communications  equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 12 inches (30 cm) to any part of the Hausted equipment including specified Hausted equipment cables.
Degradation of the performance of the Hausted equipment could result.
WARNING: If RFI causes erratic behavior, unplug the electric Hausted equipment immediately. Leave unplugged while transmission is in progress.
WARNING: The use of accessories, transducers, and cables other than those specified by the manufacturer may result in increased emissions or decreased immunity of the Hausted equipment. GF cables and accessories include motor cables, mains cable, pendant cables, and back up battery and cable.
WARNING: This equipment should not be used adjacent to or stacked with other equipment. If adjacent or stacked use with other equipment is necessary, this Hausted equipment and the other equipment should be observed to verify that they are operating normally.
WARNING: The EMISSIONS characteristics of this equipment make it suitable for use in industrial areas and hospitals (CISPR 11 class A). If it is used in a residential environment (for which CISPR 11 class B is usually required) this equipment might not offer adequate protection to radio frequency communication services. The user might need to take mitigation measures, such as relocating or reorienting the equipment.

IDENTIFICATION LABEL

The stretcher identification label identifies the stretcher serial number and model, essential information when ordering replacement parts or claiming parts under warranty. The identification label, shown above, is beneath the patient left surface at midpoint of frame. Have this information ready when calling our Customer Service or Technical Support staff at 1.770.368.4700; it will allow us to better assist you and quickly answer your questions and concerns.

UNCRATING INSTRUCTIONS

IMPORTANT — REPORT ANY SHIPPING DAMAGE IMMEDIATELY:
WARNING: Inform shipper of any damage — leave carton intact. Leave equipment in the
receiving area until inspection is complete.
NOTICE — POSSIBLE EQUIPMENT DAMAGE:
NOTICE: The crate contains fragile, expensive medical equipment. Uncrate and handle
carefully. If after uncrating the equipment you find any damage (no matter how slight),
report the damage to GF Health Products, Inc.
WARNING — PERSONAL INJURY HAZARD:
WARNING: When cutting bands, always use tool specifically designed for that purpose.
This will help avoid personal injuries possibly incurred when bands are cut and tension is
released.
ENVIRONMENTAL CONDITIONS

Operating

Temperature| 5°C to 40°C
Relative Humidity| 20% to 90% @ 86°F (30°C)
Atmospheric Pressure| 700 to 1060 hPa
Storage and Transport

Temperature| -10°C to 50°C
Relative Humidity| 20% to 90% @ 86°F (30°C)
Atmospheric Pressure| 700 to 1060 hPa

UNPACKING INSTRUCTIONS
IMPORTANT: Follow each step in the order shown in these instructions.
Your Hausted equipment has been carefully packed at our manufacturing plant to ensure safe shipment to your medical facility. There are several procedures you must follow to put your new equipment in service. These procedures only take a few minutes to complete and all are required to ensure proper operation of the equipment.

1. Cut the two bands around the shipping carton.

2. Remove the top half of the carton and cut one side of the bottom half.

3. Remove the equipment from the carton.

4. Check to see if all features of the equipment work properly. If all the features work, advance to step 5. If any features do not work properly, call GF Health Products, Inc. at 1.770.368.4700.
   Info: Plug the unit into a wall socket prior to checking any electric features. The battery will reach full charge after approximately 10 hours.

5. Clean the equipment using mild detergent to remove any dirt accumulated during shipment, and place the equipment into service.

OPERATING INSTRUCTIONS

3.1 SURGI-STRETCHER SPECIFICATIONS
Info: All dimensions, unless otherwise specified, are in inches and ±.375 (1 cm).
GF Health Products, Inc. reserves the right to change specifications without notice.

Model| Standard Width 5E82EYEST & 5E82EYEST-PD| Wide Width 5E82EYXST &
5E82EYXST-D| Bariatric 5B800ST & 5B800ST-PD
---|---|---|---
Height Range: High| 40 in. ±1 in. [101 cm ±2.5 cm]
Height Range: Low| 22 in. ±1 in. [55.8 cm] ±2.5 cm
Overall Width| 32 in. [81 cm]| 37 in. [94 cm]| 37 in. [94 cm]
Overall Length| 92.35 in. [234.6 cm]| 88.38 in. [224.3 cm]
Patient Surface Width| 25 in. [64 cm]| 30 in. [76 cm]
Patient Surface Length| 85.38 in. [224.3 cm]| 80.25 in. [203.8 cm]
Backrest
Degree of Movement| 0° – 85°
Knee Flex
Degree of Movement| 0° – 60°
Trendelenburg / Reverse
Trendelenburg| 15° ±2°
Retracto Rail Height| 14 in. [36 cm]
Retracto Rail Length| 49 in. [125 cm]| 63 in. [160 cm]
Casters| 5.9 in. [15 cm] Electric Lock / Steer
Maximum Weight Capacity
(EVENLY DISTRIBUTED)| 800 lb [363 kg]
Applied Parts:| Pads, Linens, Side Rails, Some Accessories
Mattress Pad Thickness| 3 in. [7 cm]| 5 in. [13 cm]
Electrical Specifications
Product Classification:| 1
Input Voltage:| 100V – 240V ~ 50/60 Hz
Amperage:| Max. 4.0A
Duty Cycle:| 10% (2 Min. in 18 Min.)
IP Rating:| IPX4 All Models
Grounding Protection:| Type B

3.2 FEATURES, WARNINGS AND PROPER OPERATION OPERATING INSTRUCTIONS

WARNINGS — CAUTIONS AND PROPER OPERATION (See Diagram Below)

A. WARNING: Do not sit on end — tipping may occur.

B. WARNING: The stretchers have a warning label located at the head and foot end stating: Maximum patient weight 800 lb (363 kg) for 5E82 and 5B800 models.

C. WARNING: Patient entry, egress and transfer should always be done with the brakes locked.

D. WARNING: The brakes should always be locked and patient side rails up when patient is not in transport.

E. WARNING: The patient pendant has a warning label stating: Clip pendant to rail when not in use — keep cord clear of moving parts. As is stated on the cable adjacent to the pendant.

F.   WARNING: All electric stretchers are equipped with a built-in battery backup system, but it is recommended that the unit remain plugged into wall receptacle during normal use.
The battery backup is recommended for transport and EMERGENCY only.

G. WARNING: The Fowler backrest quick-drop handle is intended to be used to lower patient during EMERGENCY situations only.

H. WARNING: Ensure rail is locked before leaving patient.

 I. WARNING: When lowering the rails, ensure patient and caregiver (or attendant) body and extremities are clear of pinch points before operating the rail.

J. WARNING: To turn on electric controls, plug into wall receptacle; to turn off, remove plug from wall receptacle. The electric powered stretchers do not have a separate on / off switch.

K. WARNING: Always disconnect the power source whenever servicing any electric powered stretcher.

L. WARNING: Keep hands clear of pinch points.

M. WARNING: Stow away power cord when not in use to prevent injury or damage.

Features (Shown in Illustration of 5E82EYST and 5E82EYEST-PD below)

Features (Shown in Illustration of 5B800ST and 5B800ST-PD below)

WARNINGS — CAUTIONS AND PROPER OPERATION (See List on Previous Page)

Features (Shown in Illustration of 5E82EXYST and 5E82EXYEST-PD below)

3.3 BRAKING AND STEERING OPERATION WITH SMART CASTER TECHNOLOGY

3.3.1 Applying the Brakes
To apply the four wheel central braking system with the pendant, press the pendant Brake On / Off button; the LED above the button then illuminates green (Figure 3.3-1), and the blue caster pedals on all four corners of the stretcher automatically lower to lock (Figure 3.3-2), and all four caster wheels will then be locked from swiveling and rotating.

Info: To prevent unintended movement, the brakes engage automatically after the unit has been stationary for 30 seconds.
To apply the four-wheel central braking system manually, gently depress the blue caster pedal at any of the four corners of the stretcher until the pedal stops (Figure 3.3-2). The remaining three pedals will then automatically lower to lock (Figure 3.3-2), and all four caster wheels will then be locked from swiveling and rotating.

**** NOTICE: DO NOT apply excessive force to pedal when manually applying brakes.

3.3.2 Unlocking the Brakes
To unlock the brakes with the pendant, press the pendant Brake On / Off button; the LED above the button then goes out (Figure 3.3-3),
the blue caster pedals on all four corners of the stretcher will then automatically rise to unlock (Figure 3.3-4), and all four caster wheels will then rotate and swivel freely.

To unlock the brakes manually, gently lift the blue caster pedal at any of the four corners of the stretcher until the pedal is in a horizontal position (Figure 3.3-4); the remaining three pedals will then automatically rise to unlock and all four caster wheels will then rotate and swivel freely.

WARNING: Ensure the brakes are locked when the patient is not being transported.
NOTICE: DO NOT apply excessive force to pedal when manually unlocking brakes.

3.3.3 Activating Advanced Steer Mode — Pendant
To activate Advanced Steer Mode with the pendant, press the pendant Steer Mode On / Off button.
The LED above the button then illuminates green (Figure 3.3-5), and the blue caster pedals automatically rise (Figure 3.3-6) at the patient foot end of the stretcher.
All four caster brakes will unlock and the stretcher will be ready for transport. Push the stretcher forward or backward — both front casters will lock into Steer-Lock position, which is ideal for pushing the stretcher from the patient head end. The stretcher will steer along a straight path, maneuver corners, and change direction with minimal effort.

Note: The steer mode function (both by pendant or manual) is disabled for stretchers with the Navigator SmartDrive System. Activation with the pendant results in an audible beep. Manual activation will immediately return to the neutral position.
Info: The casters will lock into Steer-Lock position when turned to 6 o’clock or 12 o’clock, with the stretcher’s patient foot end being 12 o’clock.

Info: Depending upon how the casters are oriented when they lock, they can lock into Steer-Lock position while trailing (6 o’clock) or leading (12 o’clock). If the casters lock in opposite orientations, steering may be more difficult.
Info: The pendant will only lock the foot end casters into Steer-Lock position.

3.3.4 Activating Advanced Steer Mode – Manually
When pushing from the head end: Activate foot end Advanced Steer Mode by lifting the blue pedal upward on either head end caster until the pedal stops (Figure 3.3-6). Both foot end pedals will then rise to lock foot end casters into Steer-Lock position, the head end pedals will return to neutral position (Figure 3.3-4), and the LED above the pendant Steer Mode On / Off button will illuminate green (Figure 3.3-5).

When pushing from the foot end : Activate head end Advanced Steer Mode by lifting the blue pedal upward on either foot end caster until the pedal stops (Figure 3.3-6). Both head end pedals will then rise to lock the head end casters into Steer-Lock position, the foot end pedals will return to neutral position (Figure 3.3-4), and the LED above the pendant Steer Mode On / Off button will illuminate green (Figure 3.3-5).
Info: It is not possible to lock the head end casters into Steer-Lock position with the pendant. This can only be done with the foot end manual activation.

3.3.5 Deactivating Advanced Steer Mode —Pendant
To deactivate Advanced Steer Mode with the pendant, press the pendant Steer Mode On / Off button. The LED above the button will go out (Figure 3.3-7) and the blue caster pedals in Steer-Lock position will automatically lower to neutral position (Figure 3.3-4). All four casters will now rotate and swivel freely.
Info: All four casters must be parallel to each other in the 6 o’clock or 12 o’clock position to be able to properly go into neutral position.
Failure to place casters in this orientation may cause the Steer Mode On / Off button to not deactivate Steer Mode.

3.3.6 Deactivating Advanced Steer Mode – Manually
Depress the blue caster pedal down to the neutral position (Figure 3.3-4) on either caster locked into Steer-Lock position. All four casters will now rotate and swivel freely. Depressing the blue pedal down past neutral until it stops will apply all four caster brakes (Figure 3.3-2), locking all four casters into brake position.

Info: After thirty seconds of no movement, Advanced Steer Mode automatically deactivates and all four caster wheels lock into brake position.
WARNING: To prevent unintended movement, activate or deactivate Advanced Steer Mode onlywhile the stretcher is stopped.

Caster Pedal Positions
The table below shows the blue caster pedal in all three positions.

CASTER PEDAL POSITIONS

| Pedal Up| Steer-Lock Position
| Pedal Horizontal| Neutral Position (Swivel)
| Pedal Down| Brake Position
(Locked)

3.4 ELECTRIC CONTROL LOCATIONS

3.4.1 Pendant Control Storage Location
The pendant is located on the bumper rail on either side of the stretcher (Figure 3.4-1).
NOTICE: Place pendant on bumper rail when not in use. Keep cord clear of moving parts.

3.4.2 Plug Location
This stretcher is equipped with a battery backup for transport but the unit should be plugged into a wall receptacle when not in transport. The plug is located on the patient right side of the stretcher (Figure 3.4-2). Do not position the unit so that it is diffi cult to disconnect the plug.

WARNING: The 5E82 Surgi-Stretcher is equipped with a built in battery backup system: nevertheless, the unit should remain plugged into wall receptacle during normal use. The battery backup is recommended for transport and emergency only.

3.4.3 Low Battery Alarm
This stretcher is equipped with an audible and visual low battery alarm. When the system requires charging, a continuous beep will sound during motor operation, the pendant LED above the BATTERY button will illuminate green, and the control box LED will illuminate amber.

3.4.4 Foot Control
Large red circle indicates optional foot control storage location (Figure 3.4-3). Small red circle indicates foot control plug-in location (Figure 3.4.3), which can also be used as an alternate pendant plug-in location.

3.5 HEIGHT AND PATIENT SURFACE ADJUSTMENT

3.5.1 LOCK / UNLOCK (button 1)

1| | Press and hold LOCK button (1) for three seconds to lock all functions. After fi ve LED fl ashes, all four UP LED’s (2-5) illuminate steady green, indicating they are now locked; an audible signal also indicates when locked and beeps up to three times until button is released.
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Press and hold LOCK and BATTERY buttons (1 and 19) for one second to unlock all functions. A quick LED fl ash indicates they are now unlocked; an audible signal also indicates when unlocked.
Press and hold LOCK button (1) and press each UP button (2-5) to unlock each function individually. As each button is released, its LED will go out, indicating that function is unlocked.

3.5.2 HEIGHT (HI / LO) (buttons 2 and 9)

2| | HEIGHT UP| Press and hold HEIGHT button (2) until desired height is achieved.
LED illuminates steady green while pressed, goes out when released.
---|---|---|---
9| HEIGHT DOWN| Press and hold HEIGHT DOWN button (9) until desired height is achieved. LED illuminates steady green while pressed, goes out
when released.

3.5 HEIGHT AND PATIENT SURFACE ADJUSTMENT

3.5.3 BACK SECTION UP / DOWN (buttons 3 and 10)

3| | BACK UP| Press and hold BACK UP button (3) until desired position is achieved. LED illuminates steady green while pressed, goes out  when released.
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10| BACK DOWN| Press and hold BACK DOWN button (10) until desired position is achieved. LED illuminates steady green while pressed, goes out when released.

3.5.4 KNEE FLEX UP / DOWN (buttons 4 and 11)

4| | KNEE FLEX UP| Press and hold KNEE FLEX UP button (4) until desired position is achieved. LED illuminates steady green while pressed, goes out when released.
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11| KNEE FLEX
DOWN| Press and hold KNEE FLEX DOWN button (11) until desired position is achieved. LED illuminates steady green while pressed,
goes out when released.

3.5 HEIGHT AND PATIENT SURFACE ADJUSTMENT

3.5.5 AUTO CONTOURING UP / DOWN (buttons 5 and 12)

5| | AUTO CONTOURING
UP| Press and hold AUTO CONTOURING UP button (5) until desired position is achieved. LED illuminates steady green while pressed, goes out when released.
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12| | AUTO CONTOURING DOWN| Press and hold AUTO CONTOURING DOWN button (12) until desired position is achieved. LED illuminates steady green while pressed, goes out when released.

3.5.6 BRAKE and STEER MODE Operation (buttons 6 and 13)

6| | BRAKE| Press BRAKE button (6) to toggle on / off. When brakes are locked (on), LED illuminates steady green; when brakes are unlocked (off), LED goes out. To prevent unintended movement, brakes lock automatically after stretcher is stationary for 30 consecutive seconds.
---|---|---|---
13| | STEER MODE| Press STEER MODE button (13) to toggle on / off. When steer mode is activated, LED illuminates steady green; when steer mode is off, LED goes out.
Note: Steer mode is not operable when brake is activated.
Note: Steer mode is disabled on stretchers equipped with the Navigator SmartDrive System.

3.5 HEIGHT AND PATIENT SURFACE ADJUSTMENT

3.5.7 TRENDELENBURG, SUPINE and REVERSE TRENDELENBURG Positions (buttons 7, 14 and 20)

7| | TRENDELENBURG| Press and hold TRENDELENBURG button (7) until desired position is achieved. Stretcher automatically lowers back and leg sections, tilts backward, and adjusts height. No LED.
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14| SUPINE| Press and hold SUPINE button (14) until desired position is achieved. Stretcher automatically levels back and leg sections and adjusts height. No LED.
20| REVERSE TRENDELENBURG| Press and hold REVERSE TRENDELENBURG button (20) until desired position is achieved. Stretcher automatically lowers back and leg sections, tilts forward, and adjusts height. No LED.

3.5.8 Memory and Preset Functions (Buttons 15-18)

15|   MEMORY| Position stretcher to desired position. Enter MEMORY MODE by pressing and holding MEMORY button (15) for three seconds until LED flashes. Once MEMORY LED flashes, simultaneously press and hold MEMORY button (15) and desired PRESET button (16, 17, or 18) until beeping stops (MEMORY LED will stop flashing and go out and PRESET LED will illuminate). Once MEMORY button and PRESET button are released, the position saves, LEDs go out, and MEMORY MODE exits. (After entering MEMORY MODE,  RESET buttons that illuminate are already programmed, but can be overwritten; PRESET buttons that don’t illuminate are not yet programmed.)
16| PRESET 1| Press and hold PRESET 1 button until saved pre-programmed position is achieved.
LED illuminates steady green while pressed, goes out when released.
17| PRESET 2| Press and hold PRESET 2 button until saved pre-programmed position is achieved.
LED illuminates steady green while pressed, goes out when released.
18| PRESET 3| Press and hold PRESET 3 button until saved pre-programmed position is achieved.
LED illuminates steady green while pressed, goes out when released.

3.5 HEIGHT AND PATIENT SURFACE ADJUSTMENT

3.5.9 BATTERY (button 19)

19| | BATTERY| LED illuminates steady green when battery discharges to 20% capacity or less.
Press and hold LOCK and BATTERY buttons (1 and 19) for one second to unlock all functions. A quick LED flash indicates they are now unlocked; an audible signal also indicates when unlocked.
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3.5.10 HOME (button 8)

8| | HOME| Press and hold HOME button (8). Stretcher automatically lowers back and leg sections and adjusts to lowest height.
No LED.
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3.5.11 Emergency Drop Back
This stretcher is equipped with a manual override function for the back section. This option should only be used in an emergency situation. To activate the emergency drop back, support the back section and pull outward on the red activating handle located on the patient right side under the seat to the rear (Figure 3.5-6).

Info: When activating the emergency drop, depending on the back angle, you may need to push the back in order to initiate movement.

3.6 HEADREST
3.6.1 Adjusting the Headrest
Grasp the right ball style knob (Figure 3.6-1), and rotate it counterclockwise to articulate the head section upward (Figure 3.6-2); rotate the knob clockwise to articulate the head section downward (Figure 3.6-3).

Once the upward articulation has been set, grasp the left ball style knob (Figure 3.6-4), and rotate the knob counterclockwise to articulate the chin tilt upward; rotate the knob clockwise to articulate the chin tilt downward (Figure 3.6-4).

Figure 3.6-2

Info: After understanding which knob creates which action, quick and smooth infinite adjustment can be achieved by rotating the knobs simultaneously (Figure 3.6-5).

3.7 COMMON OPTIONAL ACCESSORIES
3.7.1 Mounting the Wrist Rest
Insert the Wrist Rest into one of the appropriate three square sockets under the headrest (Figures 3.7-1 & 3.7-2). Rotate the T-knob on the back of the Wrist Rest (Figure 3.7-3) clockwise to lock it into place.

NOTICE: Ensure the Wrist Rest is secure before applying any pressure.

3.7.2 Adjusting the Wrist Rest
Once the Wrist Rest has been properly installed per 3.7-2, the height can be adjusted as needed. Support the Wrist Rest and loosen the black knob on the side of the support post (Figure 3.7-4).
Position the Wrist Rest to the desired height and rotation. Tighten the black knob located on the side of the support post (Figure 3.7-4).

NOTICE: Ensure the Wrist Rest is secure before applying any pressure.

3.8 PUSH HANDLES
3.8.1 Operating the Push Handles
Push Handles are stowed away when not in use (Figure 3.8-1).
Push Handles may be operated with the back in either raised or lowered position.

Rotating and Positioning the Hand Grips
In units without the Navigation SmartDrive System. The Hand Grips rotate 360° in 10° increments. To rotate a Hand Grip (Figure 3.8-2), hold it firmly, press the black button (Figure 3.8-3), rotate the Hand Grip to the desired position, and release the button. In units with Navigation SmartDrive System, the Hand Grips do not rotate 360° on the right Hand Grip. A stop has been installed on the units with Navigation SmartDrive System.

Operating the Push Handles with the Back in Raised Position
Rotate the Push Handles to the desired position with the back in raised position (Figure 3-8.5).
Operating the Push Handles with the Back in Lowered Position

Pull out and hold the Push Handle Release Plungers (Figure 3.8-4) and extend the Push Handles to the end position. Rotate the Push Handles to the desired position with the back in lowered position (Figure 3-8.6).
WARNING: To prevent unintended interference, ensure Push Handles are stowed away as shown in Figure 3.8-1 when not in use.

3.9 PERMANENTLY MOUNTED IV ROD OPERATION (ALL MODELS)
Refer to Figure 3-45.
WARNING: PERSONAL INJURY HAZARD – Ensure IV Rod is inserted completely into socket up to the arrow before applying any load.

3.9.1 Putting IV Rod in UP position

1. Grasp IV Rod and rotate upward until it stops.
2. Push down on IV Rod until it slides fi rmly into rod hinge socket.

3.9.2 Extending IV Rod

1. Rotate screw collar, or large screw collar, until loosened adequately to allow inner tube to easily slide up or down within outside tube.
2. Lift up on top of IV Rod until desired height is achieved.
3. Tighten collar screw(s) until hand tight.

3.9.3 Retracting IV Rod

1. Support extended portion of IV Rod with one hand.
2. Rotate screw collar until loosened.
3. Lower IV Rod until desired height is achieved, then retighten screw collar.
4. Repeat process with second screw collar as required.

3.10 PATIENT RAIL OPERATION (ALL MODELS)

**WARNING:** Always ensure the rail is locked in position before leaving the patient unattended.

3.10.1 Raising the Rail
Grasp the rail top cap in the middle of the rail (Figure 3-33) and lift.

3.10.2 Half Height
Grasp the rail and lift the red trigger under the litter top (Figure 3-34) while lowering the rail. When the rail starts to move down, release the trigger. Lower the rail until it locks into half height position.

3.10.3 Lowering the Rail

Grasp the rail and lift the red trigger under the litter top (Figure 34) while lowering the rail. Continue to lift the trigger until the rail is all the way down.

WARNING: When lowering the rails, ensure patient and caregiver body and extremities are clear of pinch points before operating the rail (Figure 3-35). WARNING: Ensure both rails are in upright locked position  before leaving patient.

TROUBLESHOOTING GUIDE

4.1 ELECTRIC POWERED STRETCHERS
DANGER: SHOCK HAZARD — To reduce the risk of electric shock, do not remove the cover.
Unit is to be serviced by qualifi ed service personnel (minimum 1 year medical equipment service and repair experience) only.
DANGER: SHOCK HAZARD — Always disconnect the power source whenever troubleshooting or servicing any electric powered stretcher.

Step 1: Check all motor and column plug connections at the controller.
Step 2: If a column does not move: Check the connection at the column.
Step 3: Plug a connector from the faulty component into a different socket.
If the component does not run: Replace that component.
If the component runs: Test pendant by plugging a functioning component into the non-functioning
socket on the controller. If this component does not run, replace the pendant. If replacing the pendant does not fix the problem, then replace the controller.
Nothing moves.| Step 1: Plug unit into main supply wall receptacle, then observe the pilot light on the controller.
If the pilot light is off: Replace the controller.
If the pilot light is on:
1.Check the nurse control plug connection at the controller.
2.Check the pendant control plug connection at the controller.
3.Ensure all lockout functions are deactivated.
4.Contact GF Health Products, Inc. for further help and instruction.
The unit runs when plugged into
wall receptacle, but does not run
on battery backup.| Step 1: Plug unit into a wall receptacle overnight.
If the battery doesn’t hold a charge, replace the battery (section 4.2).

4.2 BATTERY REPLACEMENT INSTRUCTIONS
Info: The 5E82 utilizes a unique battery specifi c to this unit (P/N H080812). To order, contact Graham-Field Customer Service at 1.770.368.4700.

1. Locate the battery and control box near the front column on the patient right side.
2. Using a fl at-head screwdriver, depress the battery mounting tab shown.
3. Remove the control box and battery by sliding them away from you until they become detached.
4. Using a fl at-head screwdriver, depress the control box mounting tab.
5. Seperate the battery from the control box by pulling toward yourself while supporting the control box.
6. Open the battery cord access cover using a fl athead screwdriver to depress the  two locking tabs.
7. Remove the cable from the battery and replace with a new battery, Hausted P/N H080812.
8. To reinstall the battery, repeat previous steps in reverse order.

GF Health Products, Inc. may be contacted at 1.770.368.4700 for additional information required to service or repair the equipment.

PREVENTIVE MAINTENANCE FOR THE USER

 |  |  |  |
---|---|---|---|---
Component
Pads / Mattresses| Cleaning Procedure
Wipe with damp cloth to remove any foreign material| Schedule
After
each
use
Schedule| Cleaning Agent’
Routine hospital grade disinfectants soap and water| Special Notes
Use only medium
strength cleaners
Do not steam clean or pressure wash
Stretcher| Wipe with damp cloth to remove any foreign material| Routine hospital grade disinfectants soap and water| Lubricate pivot points after cleaning
Electrical components| Wipe external surfaces ONLY with damp cloth to remove any foreign material| Routine hospital grade disinfectants, soap and water| Use only medium
strength cleaners
Mechanical stretcher components| Wipe with damp cloth to remove any foreign material| Routine hospital grade disinfectants, soap and water| Lubricate pivot points after cleaning
Mechanical accessories| Wipe with damp cloth to remove any foreign material| Routine hospital grade disinfectants. soap and water
Material| Lubricate pivot points after cleaning
Procedure|
Lubricate all moving and sliding parts and hinge points| Every 3
months| Lubricating oil, light-duty grease. wax stick lubricant or Never-Seez lubricant
A NEVER LUBRICATE ACTUATORS OR COLUMNS A
Inspect all fasteners to ensure proper fit, position and tightness, including nuts, bolts, etc.| Every 3
months| Proper size wrench and screwdriver
Inspect all surfaces and remove any sharp or burred areas; apply touch up paint where required| Metal file, proper color paint (specify color when ordering)
‘ Disinfecting and| Cleaning Upholstery – ALWAYS follow| manufacturer’s| recommended dilution
Disinfectants for vinyl
products| Phenolic disinfectants are the best choice for vinyl
Properly diluted quaternaries are also acceptable for vinyl
Quaternary / Isopropyl disinfectants ARE NOT recommended for vinyl
Disinfectants for urethane products| Quaternary disinfectants are recommended for urethane
Quaternary / Isopropyl disinfectants are recommended for urethane
Phenolics SHOULD BE AVOIDED on urethane
Disinfectants for all products| All fabrics may be cleaned with a 1:10 dilution of household bleaches containing 5.25% sodium hypochlorite as recommended by the Centers for Disease Control in Atlanta, Georgia; there is no harmful effect on the fabric
Disinfectants applied at full concentration or in highly concentrated solutions will decrease the useful life of fabric
iodophors-type disinfectants used on fabric may result in staining
Solis or Stains| Use neutral soapsuds and lukewarm water; DO NOT use harsh cleansers, solvents or detergents
Hard-To-Clean Spots| Use standard household / vinyl cleansers and a soft bristle brush on troublesome spots or stains; presoak heavy, dried-on soil
Laundering| Laundering Vinyl-laminated, Polyurethane-coated, or Rubber-coated fabric IS NOT recommended; laundering may substantially decrease the useful life of the fabric

NOTICE — POSSIBLE EQUIPMENT DAMAGE HAZARD: Steam cleaning and pressure washing of stretcher is not recommended and can void warranty. Info: For more detailed information, please contact GF Health Products, Inc. at
1.770.368.4700.
Info: GF Health Products, Inc. offers customized Preventive Maintenance Service Programs for Hausted products; contact your GF sales representative for further information.

OPTIONAL ACCESSORIES

Universal Accessories

H000E1700| IV Rod, 42″ Fixed Height
H000018| IV Rod, Telescoping Stainless 27″ to 50″ Height 2-Section with Holder
HSA080018| IV Pole Pendant Holder
H080770| IV and MONITOR ROD, Telescoping Stainless Steel
HSA400700| Surgical Accessories Rail – Pair
HSA080016| Surgical Bar Adaptor for Retracto Rail Models
HSA080025| Surgical Accessory Rail, Back Section
HSA080017| Surgical Armboard (HP141210538) with 2″ Navy Pad (HP150830167)
HSA080029| Orthopedic Hand Surgery Board
HSA080015| Acc’y, Patient Safety Strap W/ Buckle and Clip
HSA080021| Next-Gen Oxyflex Diffusion & Extraction System
HSA080010| Vertical 02 Tank Holder
HSA080014| Acc’y, FS3 Switch – Hi / Lo
HSA080022| Patient Tray – Next-Gen Stretchers
H000N4500| Folding Monitor Shelf
HOOWN4500| Folding Monitor Shelf – Extra Wide
HOOCR7B00| Folding Foot Extension / Footboard /Headboard Combination with Chart Holder – Reg. Width
HSA080023| Lateral X-Ray Cassette Holder
HOON16A00| Heel Stirrups with Mounting Adapters (pair)
HOOC16H00| Heel Stirrups (Pair)
HOOL16M00| Mounting Adapter clamps for Stirrups
H131495| Articulating Headrest 27″ (69 cm)
HPD0612| Pad Set, 6 Leg Retracto Rail – Navy
HSA400600| Oxyflex II with Flexible Support Structure and Adapter
HSA007900| Oxyflex II with Flexible Support Structure and Tuck Plate
HSA008000| Disposable Oxyflex II Diffusion Tray Including 24″ Tube (Qty 25)
EYE Only Accessories
HSA078500| Wrist Rest, Dual Lateral
HSA078600| Wrist Rest, Full U (Over the Brow)
HSP-1004-00| Wrist Rest, Tall (Gray)
HP150830447B| Headrest 2″ with Lateral Support
HP150830448B| Headrest 3″ with Lateral Support
HSA063500B| Headrest 4″ with Lateral Support
H0101ST| Headrest Set – 2″, 3″, & 4″
HOOCR6B00| Endboard with Chart Holder

WARNING: It is recommended that only accessories approved by GF Health Products, Inc.
be used with this device. The use of accessories, transducers, and cables other than those specified by the manufacturer may result in increased emissions or decreased immunity of the Hausted equipment.
Info: To order accessories, or for more detailed information on accessories, please contact GF Health Products, Inc. at 1.770.368.4700.

GF HEALTH PRODUCTS, INC. LIMITED WARRANTY FOR HAUSTED BRAND STRETCHERS AND CHAIRS

SCOPE OF WARRANTY
GF Health Products, Inc. (“GF”) warrants to the original purchaser only that it will replace or repair components, at GF’s sole discretion, that are defective in material or workmanship under normal use and service. All warranties are  conditioned upon the proper use of the products strictly in accordance with good commercial practice and applicable GF instructions and manuals, including proper use and maintenance.
To the extent that a third party warrants a  component, GF conveys all of its rights under that warranty to the original purchaser, to the extent permitted.
This limited warranty shall only apply to defects that are reported in accordance with the provisions set forth in this warranty document, within the applicable warranty period and which, upon examination by GF or its authorized representative, prove to be a warranty item. (See Obtaining Warranty Service below) This limited warranty is not transferable.
The warranted components and time periods are set forth below:

COMPONENT ………………………………………………………….. PARTS WARRANTY
Frame …………………………………………………………………………………5 years
Casters ……………………………………………………………………………….1 year
Electrical components ………………………………………………………………2 years
Hydraulics………………………………………………………………………………..1 year
Mechanical Components:………………………………………………………..3 years
Original and Replacement Upholstered Tops †: ……………………..1 year
Replacement Parts ‡: ………………………………………………………………90 days

*Labor is not included in the warranty.
† Upholstery is only warranted on material supplied by GF.
‡ The warranty period is as designated above. If a part is replaced under warranty, the original warranty period will not be affected. All other replacement parts will be subject to the warranty period specified.
The applicable warranty period shall commence from date of shipment to the original customer, unless there is an expiration date on the component in which case the warranty shall expire on the earlier of warranty period or the expiration date.

OBTAINING WARRANTY SERVICE
Customers located in the United States who wish to report a warranty issue, must contact GF directly by calling 1.770.368.4700 or by e-mailing a request to cs@grahamfield.com. Customers located outside the United States must contact  the Distributor from whom they purchased the products. In both cases, further directions will be provided once the initial contact is made. This limited warranty shall only apply to defects that are reported within the applicable warranty  period. Failure to abide by the specific directions will result in denial of the warranty claim.
The warranty does not cover and GF shall not be liable for the following:

1. Defects, damage, or other conditions caused, in whole or in part, by misuse, abuse, negligence, alteration, accident, freight damage, tampering or failure to seek and obtain repair or replacement in a timely manner;
2. Products which are not installed, used, or properly cleaned and maintained as required in the official manual for the applicable product;
3. Products considered to be of a non-durable nature including, but not limited to: filters, fuses, gaskets, lubricants, and charts;
4. Accessories or parts not provided by GF;
5. Matching of color, grain or texture except to commercially acceptable standards;
6. Changes in color caused by natural or artificial light:
7. Charges by anyone for adjustments, repairs, replacement parts, installation or other work performed upon or in connection with such products which are not expressly authorized in writing, in advance, by GF;
8. Any labor or shipping charges incurred in the replacement part installation or repair;
9. Costs and expenses of regular maintenance and cleaning; and
10. Representations and warranties made by any person or entity other than GF.

ENTIRE WARRANTY, EXCLUSIVE REMEDY AND CONSEQUENTIAL DAMAGES DISCLAIMER
THIS WARRANTY IS GF’S ONLY WARRANTY AND IS IN LIEU OF ALL OTHER WARRANTIES, EXPRESS OR IMPLIED. GF MAKES NO IMPLIED WARRANTIES OF ANY KIND INCLUDING ANY IMPLIED WARRANTIES OF  MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE.
IF ANY MODEL OR SAMPLE WAS SHOWN TO THE CUSTOMER, SUCH MODEL OR SAMPLE WAS USED MERELY TO ILLUSTRATE THE GENERAL TYPE AND QUALITY OF THE PRODUCT AND NOT TO REPRESENT THAT  THE PRODUCT WOULD NECESSARILY CONFORM TO THE MODEL OR SAMPLE IN ALL RESPECTS. THIS WARRANTY IS LIMITED TO THE REPAIR OR REPLACEMENT OF THE DEFECTIVE PARTS. GF SHALL NOT BE LIABLE  FOR AND HEREBY DISCLAIMS ANY DIRECT, SPECIAL, INDIRECT, INCIDENTAL, EXEMPLARY OR CONSEQUENTIAL DAMAGES, INCLUDING, BUT NOT LIMITED TO: DAMAGES FOR LOSS OF PROFITS OR INCOME, LOSS OF USE, DOWNTIME, COVER, OR EMPLOYEE OR INDEPENDENT CONTRACTOR WAGES, PAYMENTS AND BENEFITS. CERTAIN STATES MAY CONFER ADDITIONAL RIGHTS REGARDING WARRANTIES AND IN  THOSE STATES GF’S LIABILITY AND THE LIABILITY OF GF’S SUPPLIERS, SHALL BE LIMITED TO THE FULLEST EXTENT PERMITTED BY LAW.
The warranties contained herein, together with GF’s current Terms and Conditions, contain all the representations and warranties with respect to the subject matter of this document, and supersede all prior negotiations, agreements and understandings with respect thereto.
The recipient of this document hereby acknowledges and represents that it has not relied on any representation, assertion, guarantee, warranty, collateral contract or other assurance, except those set out in this document.
For additional information on this product or this warranty, please contact a GF Customer Service Representative.

NOTES:

1. Additional terms and conditions may apply. See GF’s General Terms and Conditions on its website: www.grahamfield.com.
2. Freight claims must be notated on the appropriate shipping documents and must be made with immediacy. International, federal and state regulations govern specific requirements for freight claims. Failure to abide by those  regulations may result in a denial of the freight claim. GF will assist you in filing the freight claim.
3. Claims for any short shipment must be made within three (3) days of the invoice date.

DISPOSAL AND KEY TO SYMBOLS

DISPOSAL
Hausted equipment and accessories can be disposed of.
We recommend disassembling and dividing the equipment and components into diff erent waste groups such as: metal, cable, electronic, recoverable resource and plastic for recycling or combustion.
Most plastic components are provided with a plastic types code and fi ber content to aid sorting of plastic parts.

Product| Metal Scrap| Cable Scrap| Electronic Scrap| Plastic Recycling or Combustion
---|---|---|---|---
5E82EYEST / 5E82EYXST| X| X| X| X
5B800ST| X| X| X| X

Info: Dispose of lithium battery attached to the control box in accordance with local regulations.
KEY TO SYMBOLS
The following symbols are used on Hausted product labels.

| Protective Earth| | Manufacturer
---|---|---|---
| Earth Ground| | Keep Dry
| General Warning Sign| | Fragile, Handle with Care
| CE Mark| | Electrical and Electronic Equipment
| ETL| | Consult Instructions for Use
| European Authorized Representative| | Caution
| Disconnect before Service| | Pinch Point
| Medical Device| | Unique Device Identifier
| Type B Applied Part

www.hausted.com
www.grahamfield.com

APPENDIX

9.1 GUIDANCE AND MANUFACTURER’S DECLARATION —ELECTROMAGNETIC EMISSIONS

The Hausted Stretchers are intended for use in the electromagnetic environment specified below. The customer or the user of the Hausted Stretchers should assure that they are used in such an environment.

Emissions Test| Compliance| Electromagnetic Environment – Guidance
RF emissions CISPR 11| Group 1| The Hausted Stretchers use RF energy only for their internal function. Therefore, their RF emissions are very low and are not likely to cause any interference in nearby  electronic equipment.
The Hausted Stretchers are suitable for use in all establishments other than domestic and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purposes.
RF emissions CISPR 11| Class A
Harmonic emissions IEC 61000-3-2| Class A
Voltage fluctuations / flicker emissions IEC 61000-3-3| Complies

9.2 ENCLOSURE PORT 1

Phenomenon| Basic EMC
standard or test
method| IMMUNITY TEST LEVELS
---|---|---
Professional healthcare facility environment
ELECTROSTATIC| IEC 61000-4-2| ± 8 kV contact
DISCHARGE| |
| | ± 2 kV, ± 4 kV, ± 8 kV, ± 15 kV air
Radiated RF EM fields a)| IEC 61000-4-3| 3 V/m f)
| | 80 MHz — 2,7 GHz b)
| | 80 % AM at 1 kHz C)
Proximity fields from RF wireless
communications equipment| IEC 61000-4-3| See Table 9.3.
RATED power frequency magnetic fields cl) e)| IEC 61000-4-8| 30 Alm g9 50 Hz or 60 Hz

a) The interface between the PATIENT physiological signal simulation, if used, and the ME EQUIPMENT or ME SYSTEM shall be located within 0,1 m of the vertical plane of the uniform field area in one orientation of the ME EQUIPMENT or ME SYSTEM.
b) ME EQUIPMENT and ME SYSTEMS that intentionally receive RF electromagnetic energy for the purpose of their operation shall be tested at the frequency of reception. Testing may be performed at other modulation frequencies identified by the RISK MANAGEMENT PROCESS. This test assesses the BASIC SAFETY and ESSENTIAL PERFORMANCE of an intentional receiver when an ambient signal is in the passband. It is understood that the receiver might not achieve normal reception during the test.
c) Testing may be performed at other modulation frequencies identified by the RISK MANAGEMENT PROCESS.
d) Applies only to ME EQUIPMENT and ME SYSTEMS with magnetically sensitive components or circuitry.
e) During the test, the ME EQUIPMENT or ME SYSTEM may be powered at any NOMINAL input voltage, but with the same frequency as the test signal (see Table 1).
f) Before modulation is applied.
g) This test level assumes a minimum distance between the ME EQUIPMENT or ME SYSTEM and sources of power frequency magnetic field of at least 15 cm. If the RISK ANALYSIS shows that the ME EQUIPMENT or ME SYSTEM will  be used closer than 15 cm to sources of power frequency magnetic field, the IMMUNITY TEST LEVEL shall be adjusted as appropriate for the minimum expected distance.

9.3 ENCLOSURE PORT IMMUNITY TO RF WIRELESS COMMUNICATIONS EQUIPMENT 1

frequency
(MHz)| Band a)
(MHz)| Test Service a)| Modulation b)| power
(W)| Distance
(m)| IMMUNITY
TEST LEVEL
(V/m)
---|---|---|---|---|---|---
385| 380 —390| TETRA 400| Pulse
0i
modulation
l
duaton 18 Hz| 1,8| 0,3| 27
450| 430 — 470| GMRS 460,
FRS 460| FM0
± 5 kHz deviation
1 kHz sine| 2| 0,3| 28
710| 704 — 787| LTE Band 13,
17| Pulse
modulation 0
217 Hz| 0,2| 0,3| 9
745
780
810| 800 — 960| GSM 800/900,
TETRA 800,
iDEN 820,
CDMA 850,
LTE Band 5| Pulse
modulation 0
18 Hz| 2| 0,3| 28
870
930
1720| 1 700 —
1 990| GSM 1800;
CDMA 1900;
GSM 1900;
DECT;
LTE Band 1, 3,
4, 25; UMTS| Pulse
modulation 0
217 Hz| 2| 0,3| 28
1845
1970
2450| 2 400 —
2 570| Bluetooth,
WLAN,
802.11 b/g/n,
RFID 2450,
LTE Band 7| Pulse
modulation 0)
217 Hz| 2| 0,3| 28
5240| 5 100 —
5 800| WLAN 802.11
a/n| Pulse
modulation 0
217 Hz| 0,2| 0,3| 9
5500
5785

9.4 CONTINUED

a) The test may be performed at any one power input voltage within the ME EQUIPMENT or ME SYSTEM RATED voltage range. If the ME EQUIPMENT or ME SYSTEM is tested at one power input voltage, it is not necessary to re-test at additional voltages.
b) All ME EQUIPMENT and ME SYSTEM cables are attached during the test.
c) Calibration for current injection clamps shall be performed in a 150 Ω system.
d) If the frequency stepping skips over an ISM or amateur band, as applicable, an additional test frequency shall be used in the ISM or amateur radio band. This applies to each ISM and amateur radio band within the specified frequency range.
e) Testing may be performed at other modulation frequencies identified by the RISK MANAGEMENT PROCESS.
f) ME EQUIPMENT and ME SYSTEMS with a d.c. power input intended for use with a.c.-to-d.c. converters shall be tested using a converter that meets the specifications of the MANUFACTURER of the ME EQUIPMENT or ME SYSTEM.  The IMMUNITY TEST LEVELS are applied to the a.c. power input of the converter.
g) Applicable only to ME EQUIPMENT and ME SYSTEMS connected to single-phase a.c. mains.
h) E.g. 10/12 means 10 periods at 50 Hz or 12 periods at 60 Hz.
i) ME EQUIPMENT and ME SYSTEMS with RATED input current greater than 16 A / phase shall be interrupted once for 250/300 cycles at any angle and at all phases at the same time (if applicable). ME EQUIPMENT and ME SYSTEMS  with battery backup shall resume line power operation after the test. For ME EQUIPMENT and ME SYSTEMS with RATED input current not exceeding 16 A, all phases shall be interrupted simultaneously.
j) ME EQUIPMENT and ME SYSTEMS that do not have a surge protection device in the primary power circuit may be tested only at ± 2 kV line(s) to earth and ± 1 kV line(s) to line(s).
k) Not applicable to CLASS II ME EQUIPMENT and ME SYSTEMS.
l) Direct coupling shall be used.
m) r.m.s., before modulation is applied.
n) The ISM (industrial, scientific and medical) bands between 0,15 MHz and 80 MHz are 6,765 MHz to 6,795 MHz; 13,553 MHz to 13,567 MHz; 26,957 MHz to 27,283 MHz; and 40,66 MHz to 40,70 MHz. The amateur radio bands  between 0,15 MHz and 80 MHz are 1,8 MHz to 2,0 MHz, 3,5 MHz to 4,0 MHz, 5,3 MHz to 5,4 MHz, 7 MHz to 7,3 MHz, 10,1 MHz to 10,15 MHz, 14 MHz to 14,2 MHz, 18,07 MHz to 18,17 MHz, 21,0 MHz to 21,4 MHz, 24,89 MHz to 24,99  MHz, 28,0 MHz to 29,7 MHz and 50,0 MHz to 54,0 MHz.
o) Applicable to ME EQUIPMENT and ME SYSTEMS with RATED input current less than or equal to 16 A / phase and ME EQUIPMENT and ME SYSTEMS with RATED input current greater than 16 A / phase.
p) Applicable to ME EQUIPMENT and ME SYSTEMS with RATED input current less than or equal to 16 A / phase.
q) At some phase angles, applying this test to ME EQUIPMENT with transformer mains power input might cause an overcurrent protection device to open. This can occur due to magnetic flux saturation of the transformer core after the voltage dip. If this occurs, the ME EQUIPMENT or ME SYSTEM shall provide BASIC SAFETY during and after the test.
r) For ME EQUIPMENT and ME SYSTEMS that have multiple voltage settings or auto ranging voltage capability, the test shall be performed at the minimum and maximum RATED input voltage. ME EQUIPMENT and ME SYSTEMS with a RATED input voltage range of less than 25 % of the highest RATED input voltage shall be tested at one RATED input voltage within the range. See Table 1 Note c) for examples calculations.

9.5 PATIENT COUPLING PORT

Phenomenon| Basic EMC
standard| IMMUNITY TEST LEVELS
---|---|---
Professional healthcare facility environment
ELECTROSTATIC DISCHARGE c)| IEC 61000-4-2| ± 8 kV contact
± 2 kV, -± 4 kV, ± 8 kV, ± 15 kV air
Conducted disturbances induced by RF
fields a)| IEC 61000-4-6| 3 V b)
0,15 MHz — 80 MHz
6 V b) in ISM bands between 0,15 MHz and 80 MHz
80 % AM at 1 kHz

a) The following apply:
– All PATIENT-COUPLED cables shall be tested, either individually or bundled
– PATIENT-COUPLED cables shall be tested using a current clamp unless a current clamp is not suitable. In cases were a current clamp is not suitable, an EM clamp shall be used.
– No intentional decoupling device shall be used between the injection point and the PATIENT COUPLING POINT in any case.
– Testing may be performed at other modulation frequencies identified by the RISK MANAGEMENT PROCESS .
– Tubes that are intentionally filled with conductive liquids and intended to be connected to a PATIENT shall be considered to be PATIENT-COUPLED cables.
– If the frequency stepping skips over an ISM or amateur radio band, as applicable, an additional test frequency shall be used in the ISM or amateur radio band. This applies to each ISM and amateur radio band within the specified frequency range.
– The ISM (industrial, scientific and medical) bands between 0,15 MHz and 80 MHz are 6,765 MHz to 6,795 MHz; 13,553 MHz to 13,567 MHz; 26,957 MHz to 27,283 MHz; and 40,66 MHz to 40,70 MHz. The amateur radio bands  between 0,15 MHz and 80 MHz are 1,8 MHz to 2,0 MHz, 3,5 MHz to 4,0 MHz, 5,3 MHz to 5,4 MHz, 7 MHz to 7,3 MHz, 10,1 MHz to 10,15 MHz, 14 MHz to 14,2 MHz, 18,07 MHz to 18,17 MHz, 21,0 MHz to 21,4 MHz, 24,89 MHz to 24,99  MHz, 28,0 MHz to 29,7 MHz and 50,0 MHz to 54,0 MHz.
b) r.m.s., before modulation is applied
c) Discharges shall be applied with no connection to an artificial hand and no connection to PATIENT simulation.
PATIENT simulation may be connected after the test as needed in order to verify BASIC SAFETY and ESSENTIAL PERFORMANCE.

9.6 SIGNAL INPUT/OUTPUT PARTS PORT 1

Phenomenon| Basic EMC
standard| IMMUNITY TEST LEVELS
---|---|---
Professional healthcare facility environment
ELECTROSTATIC DISCHARGE e)| IEC 61000-4-2| ± 8 kV contact
± 2 kV, ± 4 kV, -± 8 kV, ± 15 kV air
Electrical fast transients /
bursts b) I)| IEC 61000-4-4| ± 1 kV
100 kHz repetition frequency
Surges Line-to-ground a)| IEC 61000-4-5| -± 2 kV
Conducted disturbances induced by RF fields b) d) g)| IEC 61000-4-6| 3 V h)
0,15 MHz — 80 MHz
6 V h) in ISM bands between 0,15 MHz and 80 MHz i)
80 % AM at 1 kHz C)

a) This test applies only to output lines intended to connect directly to outdoor cables.
b) SIP/SOPS whose maximum cable length is less than 3 m in length are excluded.
c) Testing may be performed at other modulation frequencies identified by the RISK MANAGEMENT PROCESS.
d) Calibration for current injection clamps shall be performed in a 150 Ω system.
e) Connectors shall be tested per 8.3.2 and Table 4 of IEC 61000-4-2:2008. For insulated connector shells, perform air discharge testing to the connector shell and the pins using the rounded tip finger of the ESD generator, with the exception that the only connector pins that are tested are those that can be contacted or touched, under conditions of INTENDED USE, by the standard test finger shown in Figure 6 of the general standard, applied in a bent or straight  position.
f) Capacitive coupling shall be used.
g) If the frequency stepping skips over an ISM or amateur radio band, as applicable, an additional test frequency shall be used in the ISM or amateur radio band. This applies to each ISM and amateur radio band within the specified  frequency range.
h) r.m.s., before modulation is applied.
i) The ISM (industrial, scientific and medical) bands between 150 kHz and 80 MHz are 6,765 MHz to 6,795 MHz; 13,553 MHz to 13,567 MHz; 26,957 MHz to 27,283 MHz; and 40,66 MHz to 40,70 MHz. The amateur radio bands between  0,15 MHz and 80 MHz are 1,8 MHz to 2,0 MHz, 3,5 MHz to 4,0 MHz, 5,3 MHz to 5,4 MHz, 7 MHz to 7,3 MHz, 10,1 MHz to 10,15 MHz, 14 MHz to 14,2 MHz, 18,07 MHz to 18,17 MHz, 21,0 MHz to 21,4 MHz, 24,89 MHz to 24,99 MHz,  28,0 MHz to 29,7 MHz and 50,0 MHz to 54,0 MHz.

9.7 RECOMMENDED SEPARATION DISTANCES BETWEEN PORTABLE AND MOBILE RF COMMUNICATIONS EQUIPMENT AND HAUSTED STRETCHERS
The Hausted Stretchers are intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the Hausted Stretchers can help prevent electromagnetic interference by  maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the Hausted Stretchers as recommended below, according to the maximum output power of the communications equipment.

Rated maximum output power of transmitter (W)| Separation distance according to frequency of transmitter (m)
---|---
150 kHz to 80 MHz d = 1.21/P| 80 MHz to 800 MHz d = 1.21/P| 800 MHz to 2.7 GHz d = 2.31/P
0,01| 0.12| 0.12| 0.23
0,1| 0.38| 0.38| 0.73
1| 1.| 1.| 2.
10| 4.| 4.| 7.
100| 12| 12| 23

For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.
NOTE 1: At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects, and people.

9.8 NOTES TO SECTION 9
1. 60601-1-2 © IEC:2014

References

• Telepathy - Powering Successful Brands
• Graham-Field | Home
• Home - Hausted Patient Handling Solutions

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