HYDRAULIC ADJUSTABLE HEIGHT TRANSPORT
STRETCHER 72850020 - 7285RT20
REVISION TABLE
Revision
Data
Note
0.0
10/08/2016
First edition
1.0
28/06/2021
CE marking in accordance with
Regulation (EU) 2017/745
1.1
17/06/2022
BD/RDM ID code change in
re-notification
1.2
27/04/2023
Updating banks and
push handle
Update statement of
compliance by inserting SRN
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ID08558 - Rev. 1.3 - 14/02/2023
SUMMARY
1. GENERAL PROVISIONS ..................................................................... 6
1.1
Presentation of the manual ..................................................................................... 6
1.2
Customer Service Support ...................................................................................... 6
1.3
Conventions ............................................................................................................ 6
2. GENERAL NOTICES ............................................................................ 7
2.1
Manufacturer ........................................................................................................... 7
2.2
Intended use ........................................................................................................... 7
2.3
Environmental limits of use ..................................................................................... 7
2.4
Expected life ............................................................................................................ 7
2.5
Identifying .............................................................................................................. 8
2.6
Identification of controls ......................................................................................... 8
3. SAFETY ................................................................................................ 9
3.1
General provisions .................................................................................................. 9
4. GENERAL DESCRIPTION ................................................................. 10
4.1
Description of the stretcher ................................................................................... 10
4.2
Technical characteristics ....................................................................................... 11
5. INSTALLATION .................................................................................. 12
5.1
Transport and delivery .......................................................................................... 12
5.2
Lifting .................................................................................................................... 12
5.3
Storage ................................................................................................................. 13
5.4
Installation ............................................................................................................. 13
5.5
Verification of the allocation ................................................................................. 13
5.6
Assembly .............................................................................................................. 13
5.7
Functional test ....................................................................................................... 13
6. OPERATION AND USE ...................................................................... 14
6.1
Warnings ............................................................................................................... 14
6.2
Safe position ......................................................................................................... 14
6.3
Braking and unlocking the stretcher/insertion ........................................................ 14
6.4
Moving the stretcher .............................................................................................. 15
6.5
Raising and lowering the stretcher ........................................................................ 16
6.6
Raising and lowering the backrest section ............................................................ 17
6.7
Raising and lowering the leg section ..................................................................... 18
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6.8
Trendelenburg and Reverse-Trendelenburg (7285RT20 only) ............................. 19
6.9
Handling of sides ................................................................................................... 20
7. SANITATION ...................................................................................... 21
7.1
Sanitizing products .............................................................................................. 21
7.2
Sanitization with products containing halogens ................................................... 21
7.3
Sanitizing intervals ............................................................................................... 21
7.4
Automatic sanitization .......................................................................................... 21
7.5
Manual sanitization .............................................................................................. 21
8. MAINTENANCE .................................................................................. 22
8.1
Periodic verification .............................................................................................. 22
8.2
Technical assistance ............................................................................................. 22
8.3
Provision for .......................................................................................................... 22
8.4
Demolition and disposal ........................................................................................ 23
8.5
Products for the sanitization ................................................................................. 23
9. GUARANTEE ..................................................................................... 23
10. ACCESSORIES .................................................................................. 24
10.1
4 hooks adjustable IV rod cod. 72850032 ........................................................... 24
10.2
Basket for Stretchers cod. 72850048 .................................................................. 26
10.3
Oxygen tank basket for stretcher cod. 72850047 ................................................ 27
10.4
Water repellent mattress for stretcher cod. 72850105 and cod. 72850126 ......... 29
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EU declaration of conformity
The manufacturer
shall:
Company: Pam Mobility s.r.l.
Address: Via Verdi, 39 - 42043 Gattatico (RE) - Italy
SRN: EN-MF-000027951
Declares, under its own and exclusive responsibility, that the device/s/s
Code
Model
ID BD/RDM
BASIC REQUIREMENTS
72850020
STRETCHER WITH VARIABLE
HEIGHT
2269834/R
80557742072850020KD
HYDRAULIC
7285RT20
STRETCHER WITH VARIABLE
HEIGHT
2269838/R
8055774207285RT20Y3
HYDRAULIC
Destination The device is intended to be used exclusively as a transport stretcher,
of use: the diagnosis, treatment and monitoring of patients under close supervision and
supervision of medical personnel.
The device cannot be used for inpatient purposes.
Use environment: within healthcare facilities.
The device may not be used in a potentially explosive atmosphere or
flammable.
Personnel for the use of the product: specialized operators and doctors.
Risk class shall:
Class I (in accordance with Regulation 1, Annex VIII to Regulation (EU) 2017/745)
It complies with the following Union legislative acts:
(EU) 2017/745 Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April
2017 on medical devices amending Directive 2001/83/EC, Regulation (EC) No
178/2002 and Regulation (EC) No 1223/2009. and repealing Council Directives
90/385/EEC and 93/42/EEC
The device is subject to the conformity assessment procedure provided for in Article 52, point 7 of
Regulation (EU) 2017/745
Gattatico, Managing Director
27 April 2023 Andrea Muzzini
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1. GENERAL PROVISIONS
1.1
Presentation of the manual
This manual is intended to provide the user with all the necessary information so that, in
addition to proper use of the device, it is able to manage the same in the most autonomous
and safe way possible.
It includes information regarding technical aspects, operation, maintenance, spare parts and
safety.
Please read carefully the warnings and instructions in this manual as they provide important
information regarding SAFETY OF USE AND MAINTENANCE. Before carrying out any
operation on the device, qualified operators and technicians must read carefully the
instructions contained in this publication.
In case of doubts about the correct interpretation of the instructions, contact our office to
obtain the necessary clarification.
The descriptions and illustrations given in this publication are intended as non-binding. Pam
Mobility reserves the right to make changes that it deems convenient for improvement
purposes, without committing to updating this documentation.
The illustrations and images in this manual are intended only as examples and may differ
from practical situations.
This manual is an integral part of the device, must be kept with the utmost care by the buyer,
must be placed in the immediate vicinity of the device, in a special container and, above all,
protected from liquids and anything else that could compromise the state of readability.
The manual must accompany the device if it is given to a new user.
The content of this Manual complies with Regulation 2017/745/EU of 05.04.17 (Class I) on
medical devices.
È prohibited anyone to disclose, modify or use this manual for their own purposes.
The safety of the operator and the patient and the smooth operation of the patient depend on
compliance with the instructions described here.
1.2
Customer service
Customer Service and product support are important aspects of Pam Mobility s.r.l.
Customer Service is available for further information on the use, maintenance and service of
this product.
1.3
Conventions
The following symbols have been adopted in this manual:
ATTENTION! It is placed before certain procedures. Failure to do so may cause
damage to the article.
WARNING! It is placed before certain procedures. Failure to do so may cause
harm to the operator, the patient and the article.
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2. GENERAL NOTICES
2.1
Manufacturer
The article described in this manual is produced by:
Pam Mobility s.r.l.
Via Verdi 39 - 42043 Gattatico (RE) - Italy
Tel 0522 473859 - Fax 0522 1548244
E-mail: info@pammobility.com
http: www.pammobility.com
2.2
Intended use
The device is intended to be used exclusively as a stretcher for the transport, diagnosis,
treatment and monitoring of patients under the close supervision and supervision of medical
personnel.
The device cannot be used for inpatient purposes
Environment of use: within healthcare facilities.
The device may not be used in a potentially explosive or flammable atmosphere. Personnel
for the use of the product: specialised and medical professionals
2.3
Environmental limits of use
WARNING! The stretcher shall not be used in a potentially explosive or
flammable atmosphere.
The operating conditions of the stretcher shall be as follows:
▪ Temperature: 0
▪ Humidity: 10% 70% (not condensed).
The device must be placed in absolutely dry environment.
Environmental conditions other than those indicated may cause serious damage to the
stretcher. The placement of the stretcher in environments not corresponding to the above
makes the warranty void.
2.4
Expected life
The stretcher has been designed and constructed to operate without risk to property and
persons under the normal conditions of use defined in this manual for 10 years. However, this
duration can only be reached by complying with the requirements set out in this manual and
contacting the assistance of Pam Mobility s.r.l. whenever there is a breakdown of the
stretcher. After 10 years of use it is recommended to replace the entire stretcher.
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2.5
Identifying
ATTENTION! It is forbidden to remove the label from the device for any reason.
The article is identifiable by the plate on the base in which the following data are shown:
1. Company logo;
2. Name and address of manufacturer;
3. CE marking;
4. Lot number;
5. Date and country of manufacture;
6. Medical device;
7. Item name
8. Article code;
9. Serial number;
10. Safe working load;
11. Maximum patient weight;
12. Unique device identifier (UDI);
13. Attention: pay attention when using the medical device;
14. Read the instructions for use.
1
11 6 2
3
Pam Mobility srl
Via Verdi, 39 - 42043 Gattatico (RE) Italy
Tel. +39 0522 473859
info@pammobility.com
<Lot>
ITEM NAME
7
MD
<Description Article>
5
IT
<Year>
<ID CODE>
8
10
= Kg <P max>
<SERIAL NUMBER>
9
<Vector UDI>
12
13 14
2.6
Identification of controls
Controls and devices are identified by labels placed nearby or on the devices themselves.
= Kg
HEAVYWEIGHT
WORKLOAD
REGULATION
REGULATION
PATIENT
SECURE
BACKREST
TRENDELENBURG
DANGER
CRUSHING
LOCKING
RELEASE
BRAKES
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3. SAFETY
3.1
General provisions
WARNING! Improper use and maintenance can cause damage to people and
property.
WARNING! NOTICE FOR BLOOD BORNE DISEASES: To reduce the risk of
exposure during use of the stretcher, follow the maintenance instructions in this
manual, in addition to the safety requirements for personnel established by the
Head of the Emergency Medical Service.
Operators should read this manual carefully, follow the instructions contained in it and
familiarize themselves with the correct procedures of use and maintenance of the stretcher.
Use and carry out the maintenance of the article only as prescribed in this manual and use
only spare parts and assistance Pam Mobility s.r.l.
The stretcher, on flat paths and with patients and operators of medium stature, can be moved by
only one operator. Unusual circumstances or excessive weight of the patient may require the
intervention of other personnel, to ensure patient comfort and safety.
Do not use the stretcher for purposes other than those for which it was conceived and designed.
Always advise the patient before making any adjustment of the stretcher.
Always lock the stretcher with the brakes during the stop.
Never leave the stretcher unattended when the patient is on it.
Keep this manual for consultation and to support staff training.
Transfer it together with the product in case of sale or transition to new users.
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4. GENERAL DESCRIPTION
4.1
Description of the stretcher
Oleodynamic variable height stretchers are the Pam Mobility solution for first aid, radiology,
intensive care, surgery and endoscopy. Thanks to the wide range of accessories, suitably
chosen, it is possible to use stretchers that fully meet the needs of the target areas.
4.1.1
Names of main parts
7
8
1
2
3 4
9
5
6
5
10
1. Back section;
2. Pull handle for pushing;
3. Bumper;
4. Leg section;
5. Brake pedal;
6. Pedal up/ down;
7. Back adjustment handle;
8. Foldable sides;
9. Trendelenburg adjustment handle.
10. Wheels.
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4.2
STRETCHER
72850020
7285RT20
Sections
2
Floor size
mm
1900 x 630*
Height
mm
530 ÷ 890
Encumbrance
mm
825x2000
Back section
mm
728
Legging
mm
941
Backrest adjustment
deg
0 ÷ 71 (90)
Leg section adjustment
deg
0÷20
Angolo Trendelenburg
deg
-
0÷-18
Angle Reverse-Trendelenburg
deg
-
0÷18
Safe workload
kg
230
Patient weight
kg
Standard wheel diameter
mm
200
Maximum mattress dimensions
mm
1900x630x100
Weight
kg
110
Technical characteristics
200
*the dimensions of the table can vary according to customer requirements: width from 580 to 650 mm, length from 1950 to
2010 mm.
1 WORKING LOAD is defined as the sum of the following: patient (200 Kg), mattress and accessories (30 Kg).
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5. INSTALLATION
The handling activities described in this chapter shall only be carried out by qualified
personnel specially trained to carry out loading operations in complete safety, unloading and
handling of packages by means of lifting tools such as cranes or forklifts. Local staff should
be aware of the accident prevention rules.
5.1
Transport and delivery
Transport may be by the following means of transport: road, rail, sea, air.
The weight of the article is deductible from the technical characteristics and packaging. The
handling of the single article must be carried out using suitable means for handling such as
the self-propelled forklift or the manual forklift.
Occupational safety precautions remain valid.
The device is delivered mounted wrapped with a shockproof bubble wrap film.
ATTENTION! Upon receipt of the device, check with the conveyor that the
material is intact, has not been damaged during transport or has not been
opened voluntarily to remove parts inside. Check that the delivery corresponds
to the specifications of the order and verify with the shipping documents that the
delivery is complete.
If the packaging is damaged externally, open it in the presence of the carrier and check that
the stretcher has not been damaged.
Note any damage on the shipping documents and immediately inform Pam Mobility s.r.l.
If the packaging is not defective, please check the stretcher externally within 24 hours of
delivery.
In case of visible damage due to transport, inform the carrier and the insurer immediately, as
well as Pam Mobility s.r.l.
5.2
Lifting
WARNING! Lifting and handling operations must be carried out by specialized
personnel and trained in this type of manoeuvres.
ATTENTION! During the lifting, slowly tighten the belts and verify that no
components not prepared to bear the weight of the group are affected
In order to ensure the safe handling of the stretcher, strictly follow the following instructions:
▪ Ensure that the lifting means are adequate for the weight of the stretcher.
▪ Use only flat lifting bands.
▪ Place the lifting bands near the trolley frame and not the net frame.
▪ If forklifts are used, place the stretcher on top of a suitable platform by locking the four
wheels.
▪ Raise the stretcher from the ground as little as possible.
ATTENTION! During the operation, check that no part of the stretcher is crushed
against the lifting device.
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5.3
Storage
In case of prolonged storage, leave the stretcher sheltered from rain and wind and in a dry
place.
Protect particularly well the hydraulic parts and all parts very sensitive to humidity and low
temperatures.
The storage of the stretcher can be done in dry premises with the temperature between -10
ºF and +50 ºF; and relative humidity 20% 90% without condensation.
5.4
Installation
The installation takes place under the direction and responsibility of a qualified technician of
Pam Mobility s.r.l.
WARNING: it is absolutely forbidden to mount and install the stretcher without
the support of a qualified technician of Pam Mobility s.r.l.. Similarly it is
absolutely forbidden to disassemble the stretcher for a subsequent reinstallation
without the support of a qualified technician of Pam Mobility s.r.l.
Verify that the installation surface is sufficient considering the additional space
necessary for the assembly.
Make sure that the space left next to the stretcher is sufficient for the passage of a
persona.
Make sure that the specific capacity of the floor is sufficient to bear the weight of the
stretcher.
5.4.1
Preparation of the installation area
The place of installation must have a rigid floor, horizontal, flat.
5.5
Verification of the allocation
The packaging shall contain:
▪ variable height stretcher or variable height Plus (ordered version);
▪ additional accessories ordered;
▪ the instruction manual for use.
5.6
Assembly
ATTENTION! The assembly area must be clean and clear; must be at least 4x3 m
to allow for assembly operations.
The assembly site shall have the following characteristics:
▪ flat floor, not yielding;
▪ lighting 400 LUX.
5.7
Functional test
ATTENTION! The following check should be repeated periodically to check the
efficiency of the product.
Before using the article:
▪ perform the "periodic check" provided for in the maintenance chapter;
▪ if the check is successful the article is ready to be put on regular service, otherwise contact
Pam Mobility Customer Service immediately.
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6. OPERATION AND USE
6.1
Warnings
Sanitize the stretcher according to the procedures described in the chapter
SANITIZATION.
Inform the patient whenever the stretcher is adjusted.
Always lift the safety rails of the stretcher when a patient is on it. Always lock the
stretcher during parking by applying the brakes.
Do not use the device for purposes other than those for which it was intended
and for which it was designed.
6.2
Secure position
The stretcher is in a safe position when the bed base is in a horizontal position in the lowest
position with the sides raised and the brake applied.
6.3
Brake and unlock stretcher/insertion 5directional assist
The stretcher is equipped with four rotating braking wheels and with directional function.
With the pedal in horizontal position andwheels are free.
Pushing the pedal into position Bsi inserts the brake and the wheels are locked.
Lifting the pedal into the CSI position inserts the directional block (if any).
C
To
B
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6.4
Move the stretcher around
WARNING! Always notify the patient before moving the stretcher.
WARNING! The handling must take place only on rigid flat surfaces and with raised
sides. Always lock the stretcher at the end of handling.
To move the stretcher proceed as follows:
▪ release the brakes;
▪ ensure that the sides are raised;
▪ push or pull the stretcher by grabbing it from the push handles (2);
▪ at the end of the journey, apply the brakes.
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6.5
Raising and lowering the stretcher
WARNING! Before adjusting the height of the stretcher make sure that the brakes
are locked and the side sides raised; always notify the patient before any
adjustment.
WARNING! Do not place hands or objects between the frame and moving parts.
Do not manually intervene on moving parts and follow the instructions.
The height adjustment is obtained by means of an hydraulic pump operated by a pedal lever
on the foot side of the stretcher.
To lift the stretcher proceed as follows:
▪ Press the pedal repeatedly (6) until the desired position is reached.
To lower the stretcher proceed as follows:
▪ Lift the pedal (6) to lower the bed until the desired height is reached.
6
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6.6
Raising and lowering the back section
WARNING! Always notify the patient before adjusting the backrest of the
stretcher.
ATTENTION! Make sure that the brake is engaged before performing any
manoeuvre.
The adjustment of the backrest section of the stretcher is obtained through two gas springs
controlled by lever (7).
WARNING! Do not interpose the hands or objects between the backrest and the
frame of the bed base. Do not manually intervene on moving parts and follow the
instructions.
WARNING! Do not release the back section if you are not sure of the perfect
locking by the mechanism.
ATTENTION!! During the adjustment accompany the movement to avoid sharp
movements to the patient.
To raise the back section proceed as follows:
▪ grab the back section (1) with one hand through the handle and with the other pull the
handle (7);
▪ reached the desired position release the handle (7).
To lower the back section proceed as follows:
▪ grab the back section (1) with one hand through the handle and with the other pull the
handle (7);
▪ push the backrest section downwards until the desired position is reached and release the
handle (7).
7
1
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6.7
Raising and lowering the leg section
WARNING! Always notify the patient before adjusting the upper leg section.
ATTENTION! Make sure that the brake is engaged before performing any
manoeuvre.
The leg section is adjusted by means of a 5-position trigger mechanism.
WARNING! Do not interpose the hands or objects between the leg section and
the frame of the network plane. Do not manually intervene on moving parts and
follow the instructions.
WARNING! Do not release the leg section if you are not sure of the perfect
locking by the mechanism.
To raise the leg section (4) proceed as follows:
▪ Grasp with both hands and lift the leg section (4) until the desired position. The mechanism
is equipped with an automatic locking system with clicks and a "click" will alert you to reach
the locking point.
To lower the upper leg section (19) proceed as follows:
▪ Lift the leg section (4) completely so as to unlock the rack mechanism, then gently lower
the section to the complete support on the frame of the mesh.
4
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6.8
Trendelenburg and Reverse-Trendelenburg (7285RT20 only)
WARNING! Before adjusting the position of Trendelenburg/ controtrendelenburg
of the stretcher make sure that the brakes are locked and the side rails raised;
always notify the patient before any adjustment.
The Trendelenburg and reverse-Trendelenburg movements are adjusted by means of two
hydraulic pistons controlled by a handle (9) on the foot side of the stretcher.
WARNING! Before making any other type of adjustment, return the plane to the
horizontal position.
WARNING! Do not release the frame traverse unless you are sure of the perfect
locking by the mechanism.
ATTENTION! During adjustment accompany the movement to avoid sharp
movements to the patient.
To adjust the trendelenburgposition proceed as follows:
▪ if not in position, raise or lower the bed base up to about half height (see par.
"Raise and lower the stretcher;
▪ firmly grip the frame crossbar (11) with both hands and press the handle (9);
▪ lift the net to the end of the course to obtain the Trendelenburg position or lower it to the
end of the course to obtain the Reverse Trendelenburg position;
▪ once you have reached the desired position release the handle (9).
9 11
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6.9
Handling of sides
WARNING! Always notify the patient before making any adjustments.
ATTENTION! Make sure that the brake is engaged before performing any
manoeuvre.
WARNING! Do not insert hands or objects between the network plane and the
banks.
WARNING! Do not release the side if you are not sure of the perfect locking by
the mechanism.
To lower the sides proceed as follows;
▪ pull the red lever (12) and accompany the bank until the end of the run.
To lift the sides proceed as follows:
▪ raise the bank to the safety lock.
12
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7. SANITATION
7.1
Sanitizing products
ATTENTION! Sanitizing agents are corrosive.
The best sanitizing agents and disinfectants are those most commonly used in industry.
Follow the instructions provided by the manufacturer for the specific application during use. If
possible, ask the manufacturer for guarantees on the degree of corrosivity of the solutions
used.
Any change to these features may damage the item.
È very important to follow the specifications regarding concentration, temperature and
reaction time. Any modification of these features may damage the device.
During the sanitization steps use only:
▪ cold water;
▪ hot water max. 95 C;
▪ alkaline solutions max. 80 C;
▪ disinfectant solutions.
Do not use sulfuric acids or mineral acids such as HCl, H2SO4, HNO3and
H2SO3.
7.2
Sanitization with products containing halogens
WARNING: Do not use halogen-containing products during closed circuit
sterilization, the stretcher may be damaged.
If used incorrectly these products can corrode steel especially if the pH is low. Perform
accurate checks before using these solutions.
If the device is to be sanitized using halogen containing sanitizers (e.g.
chlorine), the following requirements shall be followed:
▪ the pH must be above 10;
▪ the temperature must not exceed 40 ºC;
▪ the solution must not remain in contact with the stretcher for more than 20 min.;
▪ a concentration of up to 50 ppm of active chlorine shall be used;
▪ after sanitizing perform a generous rinse with water.
7.3
Sanitizing intervals
The sanitising intervals shall be defined by the user, according to the requirements, taking into
account the indications given in this manual and those given in the sanitising products used.
7.4
Automatic sanitization
The stretcher is not autoclavable. Danger of damage.
7.5
Manual sanitization
ATTENTION! Always check the safety data sheets of the materials used for
sanitization. In case of contact/ inhalation and/ or ingestion, follow the
prescriptions indicated in the prescribed sheets.
The manual sanitization will be defined by the customer, according to the needs, taking into
account the indications in this manual, and those reported by the sanitizing products used.
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8. MAINTENANCE
8.1
Periodic verification
ATTENTION! If damage is detected, put the product immediately out of service
until it has been repaired or replaced.
User personnel shall inspect the article at least once a year; the inspection must
include the visual search for any damage that could compromise integrity and
proper functioning of Article. Which:
▪ integrity of sides and brakes;
▪ integrity of the stretcher structure;
▪ tightening screws;
▪ correct insertion and fixing of any accessories;
▪ wheel cleaning and general product.
8.2
Technical assistance
ATTENTION: all assistance interventions must be carried out by Pam Mobility
personnel. Assistance by unauthorized persons may impair the operation of the
stretcher and may cause damage to property or persons. Pam Mobility s.r.l.
assumes no liability for damage to property or persons resulting from assistance
provided by unauthorized personnel.
Requests for assistance from the customer service department must be sent by fax or e-mail
to the following address:
Pam Mobility s.r.l.
Via Verdi 39 - 42043 Gattatico (RE) - Italy
Tel 0522 473859 - Fax 0522 1548244
E-mail: info@pammobility.com
http: www.pammobility.com
Specifying:
▪ product code, serial number, production code, year of installation;
▪ defects found;
▪ exact address of the place where the stretcher is installed.
8.3
Provision
In the case of a long-term provision of the product, it is necessary:
▪ turn off and/or disconnect the battery;
▪ place it dry and sheltered from the sun;
▪ protect it from dust by covering it with a nylon sheet;
▪ grease the parts that could oxidize or damage in case of drying.
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8.4
Demolition and disposal
The materials of the stretcher consist essentially of:
▪ painted or galvanized steel;
▪ plastic material in abs;
▪ elastomers.
Disassemble the stretcher by separating the individual pieces according to the material with which they
are made.
È It is mandatory to dispose of the different materials in accordance with the regulations of
the country where the product is to be disposed of.
8.5
Products for the sanitization
▪ The products used for sanitation must not be discharged into urban canalizations.
▪ Inquire about the provisions in force on disposal arrangements at the local authorities.
9. GUARANTEE
For the duration of the warranty period, the manufacturer undertakes to eliminate any defects
and/or defects in the stretcher provided that it has been correctly used in accordance with the
instructions in the user and maintenance manual.
The replacement of parts with other parts that do not comply with the Pam Mobility s.r.l.
specifications, if commercial, or not provided by Pam Mobility s.r.l. if designed, make the
warranty expire, as well as the improper use of the stretcher.
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10. ACCESSORIES
10.1
4 hooks adjustable IV rod cod. 72850032
10.1.1
Technical presentation
The drip rod consists of a chromed steel tube, at the end of which there is a support with 4
hooks made of resistant plastic material.
10.1.2
Intended use
The device is intended to be installed on Pam Mobility stretchers to support IV bags or
bottles.
Use environment: within healthcare facilities.
The device may not be used in a potentially explosive or flammable atmosphere.
Personnel for the use of the product: specialized operators and doctors.
10.1.3
Names of parties
1. Asta;
2. Shaped hooks.
2
1
10.1.4
Identification
ATTENTION! It is forbidden to remove the label from the article for any reason.
The following label shall be applied to the article:
Tel. +39 0522 473859
Pam Mobility srl
Via Verdi, 39 - 42043 Gattatico (RE) Italy
info@pammobility.com
<Lot>
ITEM NAME
<Year>
<Description Article>
IT
<ID CODE>
= Kg <C.l.s.>
<SERIAL NUMBER>
for hook
<Vector UDI>
25
ID08558 - Rev. 1.3 - 14/02/2023
10.1.5
Installation of the IV support rod
WARNING! The installation of this article must be carried out by qualified
personnel.
WARNING! Orient the IV support hooks according to the longitudinal axis of the
stretcher.
To install the IV rod proceed as follows:
▪ lift the rod fixing lever (4) present in the clamp (3) of the IV rod holder bar present in the
stretcher;
▪ Insert the rod (1) into the clamp (3);
▪ Adjust the height and fix the position by lowering the lever (4).
1
4
3
10.1.6
Functional test
ATTENTION! The following check should be repeated periodically to check the
efficiency of the product.
Before using the article:
▪ check if it works correctly by referring to the "Operation and use" section of this accessory;
▪ If the check is successful, the item is ready to be put on regular service, otherwise contact
Customer Service immediately.
10.1.7
Operation and use
ATTENTION! Do not use the IV support rod for any other purpose.
WARNING! Always check that the IV support rod is correctly installed before use.
WARNING! Do not exceed the safe workload of the IV support rod.
Hang the IV with its own holder on the rod hook (2).
10.2
Basket for Stretchers cod. 72850048
10.2.1
Technical presentation
Steel basket to be placed under the backrest of the stretcher.
10.2.2
Intended use
The device is intended to be installed on Pam Mobility stretchers to hold clothing and items.
Use environment: within healthcare facilities.
The device may not be used in a potentially explosive or flammable atmosphere. Personnel
for the use of the product: specialised and medical professionals
10.2.3
Preparation of the installation area
The DIN bar basket must be installed on Pam Mobility stretchers. It is advisable to install the
accessory before placing the stretcher in service.
10.2.4
Identification
ATTENTION! It is forbidden to remove the label from the article for any reason.
The following label shall be applied to the article:
Tel. +39 0522 473859
<Vector UDI>
10.2.5
Installation of the monitor door system
WARNING! The installation of this article must be carried out by nursing staff.
To install the basket, proceed as follows:
▪ raise the backrest of the stretcher;
▪ hook the basket to the frame of the stretcher.
26 ID08558 - Rev. 1.2 - 27/04/2023
Pam Mobility srl
Via Verdi, 39 - 42043 Gattatico (RE) Italy
info@pammobility.com
<Lot>
ITEM NAME
<Description Article>
<Year>
IT
<ID CODE>
= Kg <C.l.s.>
<SERIAL NUMBER>
27
ID08558 - Rev. 1.2 - 27/04/2023
10.3
Oxygen tank basket for stretcher cod. 72850047
10.3.1
Technical presentation
The cylinder holder consists of a curved painted steel rod. The cylinder holder must be
installed on the chassis side of the stretcher head.
10.3.2
Intended use
The device is intended to be installed on Pam Mobility stretchers to support the oxygen
cylinder.
Use environment: within healthcare facilities.
The device may not be used in a potentially explosive or flammable atmosphere.
Personnel for the use of the product: specialized operators and doctors.
10.3.3
Preparation of the installation area
The cylinder holder must be installed on stretchers by Pam Mobility technical personnel. It is
advisable to install the accessory before placing the stretcher in service.
10.3.4
Identification
ATTENTION! It is forbidden to remove the label from the article for any reason.
The following label shall be applied to the article:
Tel. +39 0522 473859
Pam Mobility srl
Via Verdi, 39 - 42043 Gattatico (RE) Italy
info@pammobility.com
<Lot>
ITEM NAME
<Year>
<Description Article>
IT
<ID CODE>
= Kg <C.l.s.>
<SERIAL NUMBER>
<Vector UDI>
10.3.5
Installation of the cylinder holder
The installation of this article must be carried out by Pam Mobility technical staff.
10.3.6
Functional test
ATTENTION! The following check should be repeated periodically to check the
efficiency of the product.
Before using the article:
▪ check if it works correctly by referring to the "Operation and use" section of this accessory;
▪ If the check is successful, the item is ready to be put on regular service, otherwise contact
Customer Service immediately.
10.3.7
Operation and use
ATTENTION! Do not use the article for any purpose other than the following.
WARNING! Never exceed the safe workload of the accessory.
WARNING! Always make sure that the article is securely attached to the stretcher
before putting it into use.
WARNING! Check that the cylinder is completely free from attached medical aids.
Make sure you have adequate movement space to perform the operation safely.
WARNING! The residual risk of the cylinder falling during extraction remains.
Insert the cylinder slowly and completely into the cylinder holder.
Carefully remove the cylinder and store it in a safe place.
28 ID08558 - Rev. 1.2 - 27/04/2023
29
ID08558 - Rev. 1.2 - 27/04/2023
10.4
Water repellent mattress for stretcher cod. 72850105 and cod.
72850126
10.4.1
Technical presentation
Fireproof mattress with removable zipper lining, waterproof, washable and translucent.
Spessore 6 cm (cod. 72850105) o 8 cm (cod.72850126).
10.4.2
Intended use
The device is intended to be installed on Pam Mobility stretchers to ensure patient comfort.
Use environment: within healthcare facilities.
The device may not be used in a potentially explosive or flammable atmosphere.
Personnel intended for use of the product: specialized operators, doctors and patients.
10.4.3
Identification
WARNING! it is forbidden to remove the label from the article for any reason.
The following label shall be applied to the article:
Pam Mobility srl
Via Verdi, 39 - 42043 Gattatico (RE) Italy
Tel. +39 0522 473859
info@pammobility.com
<Lot>
ITEM NAME
<Description Article>
<Year>
IT <ID CODE>
= Kg <C.l.s.> <SERIAL NUMBER>
<Vector UDI>
10.4.4
Preparation for installation area
The mattress must be installed on Pam Mobility stretchers before placing the stretcher in
service.
Via Verdi, 39 - 42043 Gattatico (RE)
Tel. +39 0522 473859 - Fax +39 0522 1548244
info@pammobility.com - www.pammobility.com
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