ANI Monitor V1 - Continouous analgesia monitoring system
MD/PRD/IN16.ANIV1 V.10 – 29 SEP 2021
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OF RADIO FREQUENCY COMMUNICATION. THE USER MIGHT NEED TO
PERFORM CORRECTIVE ACTIONS, SUCH AS REIMPLANTATION OR
REORIENTATION OF THE ANI Monitor V1.
THE INTERFACE WIRE HAS TO BE CAREFULLY PLACED AND HELD DOWN TO
PREVENT ANY PATIENT STRANGULATION RISK.
DO NOT PLACE SKIN ELECTRODES BETWEEN DEFIBRILLATOR PADLLE WHEN
IT’S USED ON A PATIENT CONNECTED TO THE ANI Monitor V1.
USE AGAIN AN ARRAY ALREADY USED ON PREVIOUS PATIENT COULD LEAD
RISK OF CROSS-CONTAMINATION.
IF THE PATIENT DEVELOPS A CUTANEOUS RASH OR OTHERS UNUSUAL
SYMPTOMS, REMOVE THE ARRAY. IT IS IMPORTANT TO ADAPT A PARTICULAR
CARE TO PATIENTS SUFFERING FROM DERMATOLOGICAL PROBLEMS.
NEVER PUT ELECTRODES ON INJURIES.
ON ELECTRICAL SHOCK HAZARD :
-
DO NOT ATTEMPT TO DISCONNECT THE POWER CORD WITH WET
HANDS.
-
DO NOT REMOVE MONITOR COVERS DURING OPERATION OR WHILE
POWER IS CONNECTED TO MONITOR.
