Drive Medical Primus Medical PrimePlus P1752 Owner's Manual
This manual must be given to the Owner/User
of this bed and should be read carefully before
putting this product into use. Keep manual in
an accessible location for future reference.
*Bed Shown with Optional Head/Foot Boards
Bariatric 750 Full Electric
Long Term Care Bed
Model # P1752
Owner's Manual
Drive Medical
99 Seaview Blvd
Port Washington, NY 11050
Phone: 1.877.224.0946
Fax: 516.988.4601
www.drivemedical.com
P1752 Owner's Manual| REV 002.04.21.2015
April 21, 2015
TABLE OF CONTENTS
STANDARD SYMBOLS USED IN THIS MANUAL ........................................................................ 2
WARNING LABELS ..................................................................................................................... 3
INTENDED USE ........................................................................................................................... 4
CONTRA-INDICATIONS ............................................................................................................ 4
GENERAL SAFETY ...................................................................................................................... 4
LEFT/RIGHT REFERENCE GRAPHIC .......................................................................................... 9
ELECTROMAGNETIC EMMISSION AND IMMUNITY .............................................................. 10
FEATURES AND ACCESSORIES ............................................................................................... 13
TECHNICAL SPECIFICATIONS ................................................................................................ 14
COMPLIANCE INFORMATION ............................................................................................... 15
ASSEMBLY ................................................................................................................................ 16
FREQUENTLY USED BED FUNCTIONS ..................................................................................... 26
BED MOBILIZATION AND STABILIZATION .............................................................................. 27
CARE AND MAINTENANCE ................................................................................................... 27
INSPECTIONS ........................................................................................................................... 28
SERVICING .............................................................................................................................. 30
TROUBLESHOOTING GUIDE ................................................................................................... 32
WARRANTY .............................................................................................................................. 34
END OF LIFE DISPOSAL ........................................................................................................... 35
APPENDIX ................................................................................................................................ 36
NOTE: DO NOT operate this product without first reading and understanding this user
manual. Damage or injury may result from improper use of this product.
Page 1 The information in this document is subject to change without notice.
P1752 Owner's Manual| REV 002
April 21, 2015
STANDARD SYMBOLS USED IN THIS MANUAL
This manual includes important information about the safety of personnel and
equipment. As you read through this manual be aware of the symbols and their
meanings.
DANGER
Information that appears under the DANGER symbol concerns the protection of
personnel from direct and pending hazards that, if not avoided, will result in
immediate, serious personal injury or death in addition to damage of the equipment.
DANGER SHOCK HAZARD
Information that appears under the DANGER SHOCK HAZARD symbol concerns the
protection of personnel from possible hazards related to electrical shock.
FIRE HAZARD
Information that appears under the FIRE HAZARD symbol concerns the protection of
personnel from possible hazards related to fire and flammability.
WARNING
Information that appears under the WARNING symbol concerns the protection of
personnel from possible hazards that can result in injury or death in addition to
damage of the equipment.
CAUTION
Information that appears under the CAUTION symbol concerns the protection of
personnel from possible hazards that may result in minor injury or damage of the
equipment.
CRUSH HAZARD
Information that appears under the CRUSH HAZARD symbol concerns the protection
of personnel from possible hazards related to reduced clearances.
NOTE:
Information that appears under the NOTE text gives added information, which helps
in understanding the item being described.
The information in this document is subject to change without notice. Page 2
Symbols
Description
Symbols
Description
According to IEC 60417-5840. Type B
applied part equipment
Change head deck position
According to IEC 60529. Rating for dustprotection and identified as equipment
that is protected against splashing
water.
Change thigh/foot deck position
According to ISO 7000-1641. Operating
instructions
Change auto-contour position
Recycle the item in accordance with
local regulations.
Change hi-lo position of mattress
support platform
Intertek’s ETL listed mark for US and
Canada. A product bearing the ETL
listed Mark is determined to have met
the minimum requirements of prescribed
product safety standards.
Up
CE mark
Down
Safe Working Load
Class II equipment
Maximum Patient Weight
Flammable material symbol
Warning symbol
Warning crushing of feet
Danger: electricity, electrical hazard
symbol
Warning crushing of hands
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April 21, 2015
PRODUCT SYMBOLS
WARNING LABELS
Page 3 The information in this document is subject to change without notice.
DANGER
NEVER allow anyone under the bed at any time.
DO NOT let any body parts protrude over the side or between parts,
especially when the bed is being operated.
DANGER SHOCK HAZARD
DO NOT plug anything into the control box of bed (i.e. pendants and
actuators) while mains cable (power cord) is plugged into the wall outlet.
Any cords or tubing used on or with this bed MUST be routed and secured
properly to ensure they DO NOT become entangled, kinked or severed during
normal operation of the bed.
DO NOT roll the bed over any power or pendant cords.
P1752 Owner's Manual| REV 002
April 21, 2015
INTENDED USE
This Primus Medical by Drive Bariatric bed is intended for use within an institutional
healthcare environment, Application Environment 3 (i.e.: Skilled Nursing, Transitional
Care, Rehabilitation Care, Assisted Living).
Compliance with the regulations and guidelines as specified by your facility is
recommended.
This bed is NOT intended for patient/resident transport. Wheels are provided only to
allow movement within the patient/resident room for cleaning or patient/resident
access.
CONTRA-INDICATIONS
This bed should not be used by persons who DO NOT have the cognitive skills to
understand the information in the owner’s manual, operate the bed or control the
movements of the bed through the control interfaces. This bed should not be used
or operated by children.
GENERAL SAFETY
NOTE: In this manual, the terms patient and resident refer to a resident of a Nursing
Home, Long Term Care, Assisted Living or Rehabilitation facility.
The information in this document is subject to change without notice. Page 4
DANGER SHOCK HAZARD
This bed is equipped with a three-prong grounding plug for protection against
possible shock hazard. DO NOT under any circumstances cut or remove the
grounding prong.
DO NOT open any actuators, control boxes or pendants. Service is only to be
performed by authorized service personnel. If unauthorized service is
performed on any components the warranty is void.
Inappropriate handling of power supply cords can create a shock hazard.
When routing cables from other equipment in the medical bed, precautions
shall be taken to avoid squeezing those between parts of the medical bed.
DO NOT use an extension cord.
DO NOT allow the cord, electrical outlets, and electrical control box or hand
pendant to become wet or submerged.
DO NOT operate the bed if any electrical component such as the power
cord, electrical outlet, connections, motor/actuator or mechanical
component has malfunctioned or has been damaged in any way.
To avoid risk of electric shock, this equipment must only be connected to a
supply mains with protective earth.
FIRE HAZARD
DO NOT use near open flame or explosive gases.
Possible Fire Hazard if used with nasal mask in 1/2 bed tent 0
2
administering
equipment. If 02 tent is being used it should not fall below the mattress deck.
The pendant should not be placed in an oxygen enriched environment such
as an 02 tent.
This bed should not be placed in an oxygen enriched environment.
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April 21, 2015
Page 5 The information in this document is subject to change without notice.
WARNING
DO NOT operate this product without first reading and understanding this user
manual. Damage or injury may result from improper use of this product.
Possible injury or Death may occur if accessories are not provided by Primus
Medical by Drive. Please contact Primus Medical by Drive for accessories that
are compatible with this bed.
Possible injury or Death may occur if replacement parts are not provided by
Primus Medical by Drive. Please contact Primus Medical by Drive for
replacement parts compatible with this bed.
Possible injury or Death may occur due to pendant cord being a source for
entangling patient/resident. Patients/residents with decreased mental acuity
should NOT have access to pendant.
Unplug bed or stop pressing pendant button when bed does not function as
expected.
NEVER permit more than one (1) person in/on the bed at any time. NEVER
exceed the weight capacity of this bed. The weight capacity of this bed is
750lbs (340kg) including accessories and options (not all accessories and
options can be used at the same time).
Assumes: Max Patient/Resident Weight 582 lbs (264 kg)
Assist Rail (pair) 35lbs (16kg)
Assist Rail (4) 70lbs (32kg)
Head/Foot Board 41lbs (18.5kg)
Pendant 1.1lbs (0.5kg)
Mattress weight 55lbs (25kg)
Trapeze 97lbs (44kg)
The medical bed should be left in its lowest position except when care is
being provided in order to reduce risk of injury due to falls.
The bed MUST be connected to an appropriate power source. Unless
equipped with the optional battery backup, this bed will not operate when
not plugged in. Mains cable and proper function must be checked regularly.
Possible Injury or Death may occur if bed is pushed over abrupt thresholds
while bed is occupied. This bed is not intended for patient/resident transport.
Please use an approved resident transport device when moving a resident
P1752 Owner's Manual| REV 002
April 21, 2015
The information in this document is subject to change without notice. Page 6
CAUTION
This medical bed is not intended to work with patient lifts other than those
specified by Primus Medical by Drive as being compatible.
DO NOT use assist rails as handles for moving the bed.
Keep all moving parts; including the mattress deck (sleep surface), main
frame, all drive actuators and moving components free of obstructions.
Ensure that the individual using this bed is properly positioned, particularly
when the bed is being operated.
Body weight should be evenly distributed over the sleeping surface of the
bed. Avoid situations where entire body weight is on a raised head or foot
surface. This includes while assisting the resident in repositioning or transferring
in or out of bed.
NEVER allow anyone under the bed at any time.
Supervision is required when this product is operated by or near children or
people with disabilities.
DO NOT let any limbs or body parts protrude over the side or between bed
components, especially when the bed is being moved or operated.
Caster locks shall be used except when bed is being moved. Bed is not
intended for patient/resident transport.
Bed should be at lowest suitable height for entry and exit.
Assembly of this bed and modifications made during the actual service life
require evaluation to comply with the requirements of IEC 60601-1 and IEC
60601-2-52. No modification of this equipment is allowed.
Only items that have been specified as part of this bed or that have been
specified as being compatible with this bed shall be connected to it.
This bed frame complies with EMC requirements of IEC 60601-1-2. Radio
transmitting equipment, cell phones or similar electronic devices, used in
proximity of the bed, may affect the beds performance.
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April 21, 2015
Page 7 The information in this document is subject to change without notice.
P1752 Owner's Manual| REV 002
April 21, 2015
ENTRAPMENT WARNING
Accurate assessment of the resident and monitoring of correct maintenance and
equipment use are required to prevent entrapment. For additional information on
product and safety issues for bed frames and rails refer to product manuals specific
to the product or accessories you have or are planning to install. If bed frames have
been serviced or any other adjustments have been made, you must ensure all parts
are securely back in place before operating the bed. Other manufacturers assist
rails may not be compatible and can lead to entrapment issues or harm to residents
and staff. Make sure mattress is the correct size for bed frame and the assist rails are
secured to frame to decrease the risk of entrapment.
On March 10, 2006, the U.S. Food and Drug Administration (FDA) released guidelines
for reducing the risk of hospital bed entrapment entitled; “Hospital bed System
Dimensional and Assessment Guidance to Reduce Entrapment”. This guidance
document identifies potential entrapment areas within the bed frame, rails and
mattress and identifies those body parts most at risk for entrapment. It also provides
manufacturers with basic design criteria to consider when developing
hospital/convalescent beds; recommends specific test methods to assess the
conformance of existing hospital/convalescent bed systems; and answers
frequently-asked questions about entrapment issues.
The FDA Guidance document identifies specific dimensional criteria on potentially
injury-threatening gaps and spaces that can occur between bed system
components, such as side rails when improperly installed. Drive Medical’s Long
Term Care beds and approved accessories are manufactured to be in
conformance with these guidelines.
Please be aware that entrapment issues can still arise when components and
accessories are not properly installed on the bed. It is important for the provider or
facility staff to recognize they have an equal role in complying with the FDA
guidelines to help ensure resident safety and avoid injuries.
Copies of this document can be obtained from the FDA website:
http://www.fda.gov/medicaldevices/deviceregulationandguidance/guidancedoc
uments/ucm072662.htm
ASSIST RAIL WARNING
Other manufacturers assist rails may not be compatible and can lead to entrapment
issues or harm to patients/residents. Only compatible Primus Medical by Drive assist
rails may be used on this bed. Ensure mattress is the correct size for bed frame and
the assist rails are secured to frame to decrease the risk of entrapment.
The information in this document is subject to change without notice. Page 8
P1752 Owner's Manual| REV 002.04.21.2015
April 21, 2015
MATTRESS SPECIFICATIONS
WARNING
Possible ENTRAPMENT Hazard may occur if you DO NOT use the recommended
specification mattress.
Resident entrapment may occur leading to injury or death.
A mattress may not be included with this bed. Mattresses sized to the dimensions of
the mattress support platform must be used.
See Technical Specifications page for compatible mattress dimensions.
EMERGENCY EVACUATION
If your mattress has Velcro side bolsters remove them and adjust mattress
retainers inward.
Push in extension buttons and slide extensions inward towards the center of
the bed.
It may be necessary to remove assist rails to fit through your doorways.
Perform this procedure on both sides of the bed.
The bed is now at 39” width and can be used to evacuate Resident out of
the facility. This bed is NOT intended to be used for resident transport.
LEFT/RIGHT REFERENCE GRAPHIC
Page 9 The information in this document is subject to change without notice.
Guidance and manufacturer's declaration - Electromagnetic emissions
The PrimePlus™P1752 is intended for use in the electromagnetic environment specified
below. The customer or the user of the PrimePlus™P1752 should ensure that it is used in such
an environment.
Emissions Test
Compliance
Electromagnetic environment - Guidance
RF Emissions CISPR 11
Group 1
The PrimePlus™P1752 must emit
electromagnetic energy in order to perform
its intended function. Nearby electronic
equipment may be affected.
RF Emissions
CISPR 11
Class B
The PrimePlus™P1752 is suitable for use in all
establishments including domestic
establishments and those directly connected
to the public power supply network that
supplies buildings used for domestic purposes.
Harmonic Emissions
IEC 61000-3-2
Not
Applicable
Voltage fluctuations/
flicker emissions
IEC 6100-3-3
P1752 Owner's Manual| REV 002
April 21, 2015
ELECTROMAGNETIC EMMISSION AND IMMUNITY
This MEDICAL ELECTRICAL EQUIPMENT needs special precautions regarding EMC and
needs to be installed and put into service according to the EMC information
provided in the table below.
Portable and mobile RF communications equipment can affect MEDICAL
ELECTRICAL EQUIPMENT
WARNING
The use of ACCESSORIES, transducers and cables other than those specified, with
the exception of transducers and cables sold by the manufacturer of the
EQUIPMENT or SYSTEM as replacement parts for internal components, may result in
increased EMISSION or decreased IMMUNITY of the EQUIPMENT or SYSTEM.
DECLARATION - ELECTROMAGNETIC EMISSIONS
The information in this document is subject to change without notice. Page 10
Recommended separation distances between portable and mobile
RF communications equipment and the PrimePlus™P1752
The PrimePlus™P1752 is intended for use in the electromagnetic environment in which radiated RF disturbances are
controlled. The customer or the user of the PrimePlus™P1752 can help prevent electromagnetic interference by
maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the
PrimePlus™P1752 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
80 MHz to 800 MHz
800 MHz to 2,5 GHz
0.01
0.12
0.12
0.23
0.1
0.38
0.38
0.73
1
1.2
1.2
2.3
0.1
0.38
0.38
0.73
10
3.8
3.8
7.3
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) accordable to the transmitter manufacturer.
NOTE: I At 80 MHz and 800 MHz the separation distance for 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.
P1752 Owner's Manual| REV 002.04.21.2015
April 21, 2015
Page 11 The information in this document is subject to change without notice.
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