Bedienungsanleitung Gima OXY 50 (Seite 2 von 18) (Englisch)

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19 ENGLISH

Instructions to User

Dear users, thank you very much for purchasing the Pulse Oximeter (hereinafter referred to as device).

This Manual is written and compiled in accordance with the council directive MDD93/42/EEC for medical

devices and harmonized standards. In case of modications and software upgrades, the information

contained in this document is subject to change without notice.

It is a medical device, which can be used repeatedly.

The Manual describes, in accordance with the device’s features and requirements, main structure, func-

tions, specications, correct methods for transportation, installation, usage, operation, repair, mainte-

nance and storage, etc. as well as the safety procedures to protect both the user and device. Refer to

the respective chapters for details.

Please read the User Manual carefully before using this device. The User Manual which describes the

operating procedures should be followed strictly. Failure to follow the User Manual may cause measur-

ing abnormality, device damage and human injury. The manufacturer is NOT responsible for the safety,

reliability and performance issues and any monitoring abnormality, human injury and device damage

due to users’ negligence of the operation instructions. The manufacturer’s warranty service does not

cover such faults.

Owing to the forthcoming renovation, the specic products you received may not be totally in accord-

ance with the description of this User Manual. We would sincerely regret for that.

Our company has the nal interpretation to this manual. The content of this manual is subject to change

without prior notice.

Warnings

Remind that it may cause serious consequences to tester, user or environment.

 Explosive hazard—DO NOT use the device in environment with inammable gas such as anesthetic.

 DO NOT use the device while examining by MRI or CT, as the induced current may cause burn.

 Do not take the information displayed on the device as the sole basis for clinical diagnosis. The de-

vice is only used as an auxiliary means in diagnosis. And it must be used in conjunction with doctor’s

advice, clinical manifestations and symptoms.

 The maintenance to the device can only be performed by qualied service personnel specied by

manufacturer. Users are not permitted to maintain or ret the device by themselves.

 Uncomfortable or painful feeling may appear if using the device ceaselessly, especially for the micro-

circulation disturbance users. It is not recommended that the sensor is used on the same nger for

more than 2 hours.

 For some special users who need a more careful inspection on the test site, please don’t place the

device on the edema or tender tissue.

 Please do not stare at the red and infrared light emitter (the infrared light is invisible) after turning on

the device, including the maintenance staff, as it may be harmful to the eyes.

 The device contains silicone, PVC, TPU, TPE and ABS materials, whose biocompatibility has been

tested in accordance with the requirements in ISO 10993-1, and it has passed the recommended

biocompatibility test. The person who is allergic to silicone, PVC, TPU, TPE or ABS can not use this

device.

 The disposal of scrap device, its accessories and packaging should follow the local laws and regula-

tions, to avoid polluting to the local environment. And the packaging materials must be placed in the

region where the children are out of reaching.

 The device can not be used with the equipment not specied in the Manual. Only the accessories

appointed or recommended by the manufacturer can be used, otherwise it may cause injury to the

tester and operator or damage to the device.

 The SpO2 probe accompanied is only suitable for using with the device. The device can only use the

SpO2 probe described in the Manual, so the operator has the responsibility to check the compatibility

between the device and the SpO2 probe before using, incompatible accessories may cause device

performance degradation, device damage or patient injury.

 Do not reprocess the accompanying SpO2 probe.



Check the device before use to make sure that there is no visible damage that may affect user’s safety

and device performance. When there is obvious damage, please replace the damaged parts before use.

 When the message “Sensor Off” or “Sensor Fault” appears on the screen, it indicates that the SpO2

probe is disconnected or line fault occurs. Check the connection of the SpO2 probe and whether

there is damage for the probe, if necessary, please replace the probe to avoid risks. The probe fault

will not result in a safety hazard.

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