Usb Connection Cable; Device - MIR Spirodoc Bedienungsanleitung

These sensors, , with the exception of the sensor MIR code 919020 which has the MIR connector with orange arrow,
an extension cable for a proper connection to Spirodoc. Two cable lengths are available:
Cod. 919200_INV
Cod. 919210_INV
Prolonged use and/or the patient's condition may require changing the sensor site periodically. Change sensor site and check skin
integrity, blood circulation, and correct sensor alignment at least every 4 hours.
WARNING
Incorrectly applied oximetry sensors or damaged cables may cause inaccurate readings. Using a damaged oximetry
sensor may cause inaccurate readings, possibly resulting in patient injury or death. Inspect each oximetry sensor before
use.
If an oximetry sensor appears damaged, do not use it. Use another oximetry sensor or contact your authorized repair
center for assistance.
Use only MIR oximetry sensors supplied with, or specifically intended for use with Spirodoc. Use of oximetry sensors
not intended for use with the Spirodoc may cause inaccurate readings.
Oximetry measurements may be inaccurate in the presence of high ambient light. Shield the sensor area (with a surgical
towel, for example) if necessary.
WARNING
Dyes introduced into the bloodstream (for example; to perform a diagnostic tests) such as methylene blue, indocyanine
green, indigo carmine, patent blue V (PBV), and fluorescein may adversely affect the accuracy of the oximetry reading.
Any condition that restricts blood flow, such as the use of a blood pressure cuff or a device for systemic vascular
resistance, may cause the inability to determine accurate pulse rate and SpO2 readings.
Remove fingernail polish and/or false fingernails before applying SpO2 sensors. Both may cause inaccurate oximetry
measurements.
Significant levels of dysfunctional hemoglobins, such as carboxyhemoglobin or methemoglobin, may adversely affect
the accuracy of the oximetry measurement.
Optical cross-talk can occur when two or more sensors are placed in close proximity. Optical cross-talk may adversely
affect the accuracy of the oximetry readings. The danger can be eliminated by covering each site with opaque material.
Obstructions or dirt on the sensor's emitter and/or detector may cause a sensor failure or inaccurate readings. Make sure
there are no obstructions and the sensor is clean.
Autoclaving, ethylene oxide sterilizing, may cause sensor damage. Do not attempt to sterilize the sensor.
Unplug the sensor from Spirodoc before cleaning or disinfecting to prevent damaging sensor or device, and to prevent
safety hazards for the user.
1.2.5

USB connection cable

Incorrect use or application of the USB cable may produce inaccurate measurements, which will show very inaccurate values of the
patient's condition. Carefully inspect each cable before use.
Do not use cables that appear to be or are damaged. If a new cable is required, contact your local distributor.
Use only cables supplied by MIR, specifically designed to be used with Spirodoc. The use of other types of cables can lead to inaccurate
measurements.
1.2.6

Device

WARNING
The maintenance operations detailed in this manual must be fully and accurately carried out. If these instructions are
not followed this may cause measurement errors and/or an incorrect test interpretation.
Any modifications, adjustments, repairs or reconfigurations must be made by the manufacturer or by personnel
authorised by the manufacturer. Never attempt to make a repair on your own. The set-up of configurable parameters
should only be made by qualified personnel. However, an incorrect set-up of the parameters in no way endagers the
patient's health.
The use of accessories and cables other than those specified by the manufacturer may result in increased emissions or
decreased immunity of the device.
Spirodoc should not be used adjacent to or stacked with other equipment and if adjacent or stacked use is necessary,
Spirodoc should be observed to verify normal operation in the configuration in which it will be used.
If the device is connected to other instruments, to satisfy the safety requirements of the system required by the standard
CEI EN 60601-1, it is necessary to use exclusively devices compliant to the safety standard. Therefore the PC or the
printer which the Spirodoc is connected must be compliant to the standard CEI EN 60601-1.
To dispose of the Spirodoc, the accessories, any plastic consumable materials (mouthpieces) as well as the battery, use
only appropriate containers or return all such parts to the dealer or to a recycling center. All applicable local regulations
must be followed.
SPIRODOC
length 1.5 m
length 0.5 m
cod. 980156 Rev 4.2.1
spirodoc
User manual
require the use of
EN 9/48