PHYSIO-PORT
User Manual Version 2017-11-12
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This manual reflects the equipment specifications and applicable safety standards valid at the time of
printing.
All rights are reserved for devices, circuits, techniques, software programs, and names appearing in this
manual.
The quality assurance system used by PAR Medizintechnik GmbH & Co. KG in all the company facilities
complies with standard EN ISO 13485.
The safety instructions in this manual are indicated in the following way:
CAUTION
This refers to a potentially dangerous
situation failure to observe this warning may
result in injuries and/or damage to the
product.
In order to ensure the highest level of safety for patients and a minimum of interference, as well as
keeping in line with the relevant testing precision level, the device should only be used in combination
with original accessories provided by PAR Medizintechnik GmbH & Co. KG.
No warranty claims can be made in the event of any damage as a result of using other inappropriate
accessories and consumable materials.
PAR Medizintechnik GmbH & Co. KG
will only assume responsibility for devices in relation to their
safety, reliability and functioning in the following cases:
▪
Assembly, enhancements, resettings, alterations and repairs carried out by PAR
Medizintechnik GmbH & Co. KG, or at locations that have been expressly authorized by PAR
Medizintechnik GmbH & Co. KG to carry out such repairs;
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Devices that have been used in accordance with their manuals.