Uniden AM2305, Руководство пользователя

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WARNING indicates a hazardous situation which, if not avoided,
could result in death or serious injury.
•
Consult your physician before starting to measure your blood pressure.
•
Like any oscillometric blood pressure measurement devices, certain medical conditions can affect the
measurement accuracy, among others:
- Disorder of the cardiac rhythm
- Very low blood pressure
- Very low blood perfusion
- Patients in shock
- Diabetes
- Vessel anomalies
- People with electrical implants such as a cardiac pacemaker
- Women who are pregnant
- Patient who are pre-eclamptic
- Patient motion during measurement
Due to their condition the oscillometric measurement method can produce incorrect readings. This represents a
risk for your health, since values may be interpreted incorrectly. Always consult your physician to determine
what will be suitable for you.
• This product does not and is not intended to provide a medical diagnosis. Measurement results are for
reference only. Self-diagnosis and treatment, e.g. regarding medication, using measured results represents a risk
for your health. Always consult with a licensed physician for determination of appropriate medication and
dosage thereof. Follow the instructions of your physician or licensed healthcare provider.
SAFETY NOTES
WARNING
WARNING
CAUTION indicates a hazardous situation which, if not avoided,
may result in minor or moderate injury.
CAUTION
1 2
INTRODUCTION
Thank you for purchasing Uniden blood pressure monitor. Please read this manual thoroughly before use. Contact
your physician if you have any queries about your blood pressure.
This fully automatic instrument utilizes the non-invasive oscillometric method, which detects your blood
movement through you brachial artery, for measuring your blood pressure and pulse rate, and the result will
display on a digital panel. Without using a stethoscope, you can get the readings promptly and easily.
This device conforms to European Council Directive 93/42/EEC concerning medical devices. This is made
evident by the CE mark of conformity accompanies by the reference number of the designated authority.
This device complies with EN ISO 81060 standard relating to non-invasive sphygmomanometers Part 1:
Requirements and test methods for non-automated measuremnt types and EN 1060 standard relating to
non-invasive sphygmomanometers Part 3: Supplementary requirements for electro-mechanical blood
pressure measuring systems.
This device also complies with EN 60601 standard relating to medical electrical equipment – Part 1-2: General
requirements for basic safety and essential performance and essential performance – Collateral standard:
Electromagnetic compatibility – Requirements and tests.
Indication for Use
This device is for use by medical professional or home users. It is intended to measure the systolic and diastolic
blood pressure of an adult individual by using a non-invasive technique, in which an inflatable cuff is wrapped
around the upper arm.