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USER GUIDE //
STRETCHER SUPPORT SERIES PB-410
Review 2022/01
01
INTRODUCTION
01.8
Intended purpose
The product MANUAL STRETCHER SUPPORT is indicated to load, unload and position stretchers in emer-
gency vehicles while supporting them by remaining anchored during transport.
01.9
General warnings
1. The product must be used by trained personnel only, having attended specific training for this device and
not for similar products.
2. At least every 6 months, is important to verify if updated User Manuals are available or there is any change
involving your product. This information is freely available on the website http://promeba.com/
3. Training routines must be registered on a special register in which the names of those trained, of the
trainers, date and place are indicated. This register, which will certify the eligibility of the operators to use
the Promeba, S.L. device, has to be kept for a period of 10 years after the disposal of the device itself. This
register will be made available to the competent authorities and/or manufacturer if requested.
4. Promeba, S.L. is always at your disposal to plan trainings on products.
5. Before carrying out any kind of operation on the appliance (training, installation, use), the operator must
carefully read the enclosed instructions, paying particular attention to the correct safety precautions and to
the procedures to be followed for installation and for correct use.
6. If the instructions belong to another device and not the device received, inform the manufacturer imme-
diately and avoid use of the device.
7. In the case of any doubts as to the correct interpretation of the instructions, please contact Promeba, S.L.
for any necessary clarifications.
8. Do not allow untrained persons to help during the use of the device, because they could cause damage
to the patient or to themselves.
9. Regularly check the appliance and carry out the prescribed maintenance.
10. Before each use of device the perfect operating state of the device must be checked as specified in the
instruction manual. If any damage or abnormalities which could in any way influence the correct functio-
ning and the safety of the device, of the patient and/or of the user are detected, the device must be imme-
diately removed from service and the manufacturer must be contacted.
11. If any failure or incorrect functioning of the device is detected, it must be immediately substituted with
a similar item so that the rescue procedures are guaranteed without any interruption.
12. Use of the device in anyway other than described in this manual is forbidden.
13. Do not alter or modify in any way the appliance; any such interference could cause malfunctions and
injury to the patient and/or rescuer.
14. The appliance must not in any way be tampered with (modification, adjustment, addition, replace-
ment). In such cases all responsibility will be denied for any malfunctions or injuries caused by the appliance
itself; moreover CE certification and product warranty will be considered void.
15. Those who modify or have modified, prepare or have prepared medical appliances in such a way that
they no longer serve the purpose for which they were intended, or no longer supply the intended service,
must satisfy the valid conditions for the introduction onto the market.
7
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