Specific Warnings; Residual Risk; Technical Data And Components; Commissioning - Spencer TOTAL Manuel D'utilisation Et D'entretien

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  • FRANÇAIS, page 23
warranty and release the manufacturer from all liability.
• Disinfection operations must be carried out in accordance with the validated cycle parameters, as stated in the specific technical standards.
• Do not use drying machines to dry the device.
• In case of exposed and/or injured skin, cover the surfaces in contact with the patient with a surgical sheet that respects bio-compatibility regulations to protect the patient's
health.
6.

SPECIFIC WARNINGS

To use the Total device, you must also have read, understood and carefully follow all the instructions in the user manual.
• Always comply with the maximum capacity, if any, indicated in the User Manual. Maximum load capacity means the total weight distributed according to human anatomy.
When determining the total weight load on the product, the operator should consider the weight of the patient, equipment and accessories. In addition, the operator should
assess whether the overall size of the patient reduces the functionality of the product.
• Make sure that operators are in good physical condition before lifting, as listed in the User Manual.
• The maximum weight, which weighs on each operator, must comply with local health and safety requirements.
• The warranty seals, if present on the product, must not be removed; otherwise, the Manufacturer shall no longer recognise the product warranty and shall decline all
responsibility for incorrect operation or any damage caused by the product itself.
• Establish a maintenance program and periodic checks, identifying a designated reference person. The person entrusted with routine maintenance of the device must ensure
the basic requirements envisaged by the manufacturer within these operating instructions.
• All maintenance activities must be recorded and documented with the relevant technical operation reports. This documentation must be kept for at least 10 years after the
end of the device's life and must be made available to the competent authorities and/or the manufacturer when requested.
• Use only original or Spencer Italia S.r.l. approved components/replacement parts and/or accessories to carry out any operation without causing alterations or modifications
to the device. Otherwise, we decline all responsibility regarding incorrect operation or any damage caused by the device to the patient or the operator, invalidating the
warranty and invalidating compliance with EU Regulation 2017/745.
• Never leave the patient on the device unsupervised, as they could get injured.
• Avoid contact with sharp objects.
• Follow approved Emergency Medical Service procedures for patient immobilization and transportation.
• Follow approved Emergency Medical Service procedures for patient positioning and transportation.
• Before lifting, make sure that operators have a secure grip on the device.
• The device is a patient transport stretcher and cannot be used as a stationing device.
The device is not intended for spinal immobilisation and if such injuries are suspected or evident, suitable devices should be used according to the guidelines of the
relevant emergency medical service.
• Practice with an empty stretcher with a simulated patient load to make sure you are familiar with the manoeuvres.
• At least two operators for Total Kon and four operators for Total, in suitable physical conditions, are required for use of the device. They must therefore be endowed with
strength, balance, coordination, common sense and must be trained in the correct operation of the Spencer stretcher device.
• For patient loading techniques for particularly heavy patients, for operations on steep terrain or in special and unusual circumstances, the presence of more than two ope-
rators is recommended in addition to the minimum foreseen operators.
Before each use, always check the conditions of the device and its components, as specified in the user manual. In case of faults or damage that may compromise the
functionality and safety of the device, and therefore the patient and the operator, remove the device from service or replace the components that are not intact.
• Make sure that the straps are properly installed.
• Always immobilise the patient using the equipment supplied with the device. A failure to do so can cause serious damage to the patient.
• Do not move the stretcher if the weight is not properly distributed.
• Use the stretcher only as described in this user manual.
• Do not alter or modify the stretcher to adapt it to unforeseen conditions of use: doing so could result in unpredictable operation and damage to the patient or rescuers and
shall void the manufacturer's warranty and release the manufacturer from all liability.
• Pay the utmost attention to any obstacles (water, ice, debris, etc.) present on the route, as they may cause the operator to lose balance and compromise proper functioning
of the device. If you cannot clear the route, choose an alternative route.
During hoisting, the stretcher must be kept horizontal with respect to the ground. Any abnormal inclination can cause serious damage to the patient, the device and
the operator.
• If it is necessary to use ropes, winches, ladders, lifting straps or other special equipment to move the stretcher or in the presence of a rescue that is classified as high risk or
of a purely technical nature, these interventions must be carried out solely by personnel adequately trained and with proven experience in rescue.
• The Total stretcher can only be hoisted from a fixed position using the spring catch supplied with the device. Total Kon cannot be hoisted.
• Dragging the stretcher on any type of surface leads to premature deterioration of the stretcher, which reduces its useful life and initial safety conditions.
To preserve the life of the device, protect it as much as possible from UV rays and adverse weather conditions.
• Recovery stretchers are not approved for use with aircraft.
7.

RESIDUAL RISK

No residual risks, or rather risks that could arise despite compliance with all warnings in this user manual, have been identified.
8.

TECHNICAL DATA AND COMPONENTS

Note: Spencer Italia S.r.l. reserves the right to make changes to specifications without notice.
9.

COMMISSIONING

For first use, check that:
• Packaging is intact and has protected the device during transportation
• Check that all parts included in the packing list are present
• General functionality of the device
DESCRIPTION
1
Support bed
2
Patient containment belts
3
Rope
4
Extension
5
Removable handles
6
Harnesses
7
Grommets
8
Handles
9
Transport bag
EN
DE
FR
ES
PT
EL
MATERIAL
DA
Polyethylene
Polyester
Polyester
Polyester
NL
Polyester
Nylon
Brass
Polyester
PVC
13
IT

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loading

Ce manuel est également adapté pour:

Total kon

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