USER GUIDE //
EVACUATION CHAIR WITH TRACKS PS-190
Review 2021/09
8
01
INTRODUCTION
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 device; any such interference could cause malfunctions and injury
to the patient and/or rescuer.
14. The device must not in any way be tampered with (modification, adjustment, addition, replacement).
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.
16. Handle with care.
17. Ensure that all the necessary precautions are taken in order to avoid the hazards that can arise as the
result of contact with blood or body fluids.
18. Register and store with these instructions: lot number, place and date of purchase, first date of use, date
of checks, name of users, any comments.
19. When the device is being used, the assistance of qualified staff must be guaranteed.
20. Do not store the device underneath any heavy objects which could cause structural damage.
21. Store in a cool, dry, dark place and do not expose to direct sun.
22. Store and transport device in its original packaging.
23. The device must not be exposed or come into contact with any source of combustion or inflammable
agents.
24. Position and adjust the device taking care not to cause any obstruction to rescuers and or any other
rescue equipment.
25. Attention: laboratory testing, post production tests and instruction manuals cannot always consider
every possible scenario for use. This means that in some cases the performance of the product could be
notable different from results to date obtained. Instructions are continually being updated and are under
tight surveillance of fully qualified staffs with adequate technical formation.
26. Both public and private operators are obliged to report any accident involving any medical device to the
Ministry of Health and the manufacturer as specified and within the time given by European regulations.
27. Both public and private operators are obliged to inform the manufacturer of the measures to be taken
to guarantee the safety and health of patients and users of any medical device.
28. As a distributor or end user of the products manufactured and/or distributed by Promeba, S.L., you are
strictly obliged to know the legal provisions in force in the country of destination of the goods, applicable
to the devices to be supplied (including the regulations relating to technical specifications and/or safety re-
quirements) and, therefore, understand the necessary requirements to ensure compliance of the products
