Product Improvement
MEC Medical Ltd. has a policy of continued product improvement and therefore reserves the right to make
changes which may affect the information contained in the manual without giving prior notice.
Responsibilities of the User
The Purair 750 conforms to the specifications and operating procedures described in this manual and any
accompanying notices and labels only if it has been installed, used, and maintained in accordance with the
instructions. MEC Medical can only guarantee the safe function of the machine if it is regularly checked and
serviced at or above the standards specified in this manual.
If you suspect that any component of the machine is worn, defective or otherwise unfit for use, do not use the
machine under any circumstances.
Replace any broken, worn or contaminated component(s) immediately. Contact the MEC Medical distributor
from whom the machine was obtained for further service.
Responsibilities of the Manufacturer
The manufacturer accepts responsibility for the effects on safety, reliability, and performance of the
equipment only if assembly operations, extensions, adjustments, modifications, and repairs are carried out by
persons with written authorization from the manufacturer, and the equipment is used in accordance with the
instructions for use and the electrical installation of the relevant room complies with the ‘Regulations for the
Electrical Equipment of Buildings’.
If during the warranty period the equipment is serviced by an unauthorized party, the warranty will be void.
Note to Service Personnel
The Purair 750 must only be serviced by Qualified Service Personnel.
The contents of this manual are not binding. If any significant difference is found between the product and this
manual please contact MEC Medical Ltd. for further information.
To ensure correct functioning, the equipment must be serviced at regular intervals.
MEC Medical Ltd. recommends that the machine should be serviced at intervals not exceeding one year.
Qualified Service Personnel and genuine spare parts should be used for all servicing and repairs. MEC Medical
Ltd. will not otherwise assume responsibility for the materials used, the work performed or any possible
consequences of the same.
In communication with MEC Medical Ltd., quote the model and serial number of the equipment, with the
approximate date of purchase. If the unit is being returned for repair, indicate the nature of the fault or the
work you require to be carried out.
General Cautions and Warnings
The user must be familiar with the machine and its various functions before using it on a patient.
Incorrect use of the equipment described herein may result in injury to the patient. Read this manual
before operating the machine. You must be familiar with the machine and its functions before using it on
a patient.
Keep this manual with the system to refer to and to answer any questions that arise about the system’s
operation, maintenance or, if necessary, repair.
The PA750 is latex free, note that any replacement parts must not use latex.
Warning HAZARDS can result from unauthorized modification of this ME EQUIPMENT
WARNING: To avoid the risk of electric shock, this equipment must only be connected to a supply
mains with protective earth.
Warning: A potential for electromagnetic or other interference between this EQUIPMENT and other
devices
This ME Equipment is rated to over voltage category I according to IEC 60664-1
