Introduction
Document No. 992012. Issue 19 – 24.10.22 Page 2
1.3.
Device Classification
The device referenced in this document is CE marked and has been classified as a Class 1
Medical Device under the scope of both the Medical Devices Directive 93/42/EEC and the
Medical Device Regulation 2017/745.
1.4.
Serial Number Label
The serial number label is located on the base cover moulding; see Fig. 2.
1.5.
Putting the Stretcher into Service
Care should be taken when removing packaging, avoid the use of sharp implements
wherever possible.
It is important that the stretcher is working properly, fully charged (if applicable to the
model, see Section 24. Battery Charge Level Indication, Battery Charging &
Maintenance), cleaned and disinfected before it is put into service. Use this manual to
check all the functions and refer to section 40. Cleaning and Disinfecting the Stretcher.
The stretcher should only be used, for its intended use, by suitably trained personnel
who have familiarised themselves with the functions of the stretcher. Our
representatives are available for on-site consultation or training and our head office
team will be pleased to answer any queries you may have.
1.6.
Abridged Summary of Warnings and Cautions
In common with all medical devices of this nature there are inherent risks that the user
should be made aware of, including potential pinch points from moving parts. Whilst
every effort has been taken to eliminate these risks, care should be taken when using
the stretcher. It is important that the user familiarise themselves with all of the
warnings and cautions contained within this document.
If the stretcher is damaged or faulty it must be taken out of use with immediate
effect and the fault reported to Anetic Aid, your authorised dealer or maintenance
department. The stretcher must not be used until the damage or fault has been
repaired.
When leaving patients unattended the stretcher should be fully lowered to minimise
any risk of injury should the patient fall off the stretcher.
Always apply the brakes when a patient is getting on or off the stretcher, or when
transferring patients from the stretcher to another platform.
It is important to ensure that nothing impedes the side rail release lever from locking
correctly; ensure that the release lever remains visible at all times.
After raising the side rail, it is important to ensure that it has locked in position by
pushing down on the side rail; failure to ensure the side rail is properly locked could
result in injury to the patient.
If the side rail mounted IV pole is in use when either raising or lowering the side rail
it is important to check the infusion flow rate as the height of the infusion above the
patient will change by approximately 300mm (11.8”).
When the backrest is raised, the fold-away pushing handles can come in close
proximity to the patient’s head and care should be taken.
Syringe drivers (and similar devices) can be mounted to the IV pole if extreme care is
taken when lowering or lifting the side rail with additional weight attached.
