Bedienungsanleitung SunTech CT40 (Seite 6 von 52) (Englisch)

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80-0067-00-MO-RevJ 2019-01-30 SunTech CT40 User Manual | 6

Pulse Oximetry (SpO2)

ChipOx SpO2 Module: Use only pulse oximeter (SpO2) sensors supplied by SunTech Medical or original Nellcor® pulse

oximeter (SpO2) sensors supplied by Covidien® (except for forehead reflectance sensors).

Masimo® SpO2 Module: Use only original Masimo® pulse oximeter (SpO2) sensors and cables.

Check the application site of the SpO2 sensor frequently to confirm proper positioning of the sensor and to check the

circulation and skin sensitivity of the patient.

Wireless Networking

When connecting this device to a wireless network, it is important to use only the hardware specified by SunTech

Medical (see Accessories section for details). Unsupported USB accessories, including unsupported Wireless

adapters, have been intentionally disabled and will not function with this device.

Possible Adverse Reactions

In the area of the BP cuff or SpO2 sensor, allergic exanthema (symptomatic eruption) may result, including the

formation of urticaria (allergic reaction including raised edematous patches of skin or mucous membrane and

intense itching) caused by the fabric material of the cuff or sensor.

Following the application of the BP cuff, petechia formation (a minute reddish or purplish spot containing blood that

appears in the skin) or Rumpel-Leede phenomenon (multiple petechia) may appear on the arm, which may lead to

idiopathic-thrombocytopenia (spontaneous persistent decrease in the number of platelets, associated with

hemorrhagic conditions) or phlebitis (inflammation of a vein).

Warnings and Cautions

WARNING: Do not attach the cuff to a limb being used for IV infusions or any other intravascular access, therapy or

an arteriovenous (A-V) shunt. The cuff inflation can temporarily block blood flow, potentially causing harm to the

patient.

WARNING: Pressurization of the cuff can temporarily cause loss of functionality of SpO2 if simultaneously using

device on the same limb.

WARNING: Not designed for neonates.

WARNING: Do not apply the BP cuff to a limb being used for IV infusions as the cuff inflation can temporarily block

the infusion, causing harm to the patient.

WARNING: Check frequently by observing the limb that operation of the AUTOMATED SPHYGMOMANOMETER does

not result in prolonged impairment of the circulation of the patient.

WARNING: The cuff should not be applied over a wound as this can cause further injury.

WARNING: The cuff should not be placed on the arm on the side of a mastectomy. In the case of a double

mastectomy use the side of the least dominant arm.

WARNING: The CT40 is NOT defibrillator protected.

WARNING: Do not use in the presence of flammable anesthetics or other flammable substances in combination with

air, oxygen-enriched environments, or nitrous oxide.

WARNING: Do not use the device if it has failed its diagnostics self-test, or if it displays a greater than zero pressure

with no BP cuff attached or a value of oxygen saturation with no SpO2 sensor attached.

WARNING: Do not use if device is dropped and/or damaged. Have a qualified service representative check the unit

before using again.

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