ANI Monitor V1 - Continouous analgesia monitoring system
MD/PRD/IN16.ANIV1 V.10 – 29 SEP 2021
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NEITHER THE MONITOR NOR THE SKIN ELECTRODES ARE DESIGNED FOR
USE IN THE MRI ENVIRONMENT.
THIS ANI Monitor V1 COULD NOT BE IN ANY CASE CONSIDERED AS AN ECG
MONITORING SYSTEM.
CONSIDERATIONS WHEN USING ELECTRO-CONVULSIVE THERAPY (ECT)
EQUIPMENT DURING THE ANI MONITORING: place ECT electrodes as far away as
possible from the sensors to minimize the effect of interference. Some ECT equipment may
interfere with the proper functioning of the ANI Monitor V1. Check for compatibility of
equipment during patient setup.
ONLY USE THE POWER CORD SUPPLIED BY THE MANUFACTURER. NEVER
ADAPT THE PLUG FROM THE MONITOR TO FIT A NON-STANDARD OUTLET.
IF THE INTEGRITY OF THE EXTERNAL PROTECTIVE EARTH GROUND IS IN
DOUBT, THE ANI Monitor V1 SHOULD NOT BE USED.
BE SURE THE MONITOR IS INSTALLED SECURELY TO AVOID PERSONAL OR
PATIENT INJURY.
WHEN CONNECTING EXTERNAL EQUIPMENT (e.g., DATA CAPTURE
COMPUTER), THE LEAKAGE SYSTEM CURRENT MUST BE CHECKED AND MUST
BE LESS THAN THE IEC 60601-1-1 LIMIT.