ANI Monitor V1 - Continuous analgesia monitoring system
4
MD/PRD/IN16.ANIV1 V.14 - 12 MAR 2020
ENSURE PROPER CONTACT OF THE ELECTROSURGERY RETURN ELECTRODE
TO AVOID POSSIBLE BURNS ON THE PATIENT VIA ANI ELECTRODES.
THE CHARACTERISTICS OF ANI Monitor V1 EMISSIONS ALLOW IT TO BE USED
IN INDUSTRIAL AREAS AND HOSPITALS (CISPR 11 CLASS A). WHEN USED IN
RESIDENTIAL ENVIRONMENTS (FOR WHICH CISPR 11 CLASS B IS REQUIRED),
ANI Monitor V1 CANNOT GUARANTEE PROVISION OF ADEQUATE PROTECTION
OF RADIO FREQUENCY COMMUNICATION. THE USER MIGHT NEED TO
PERFORM
CORRECTIVE
ACTIONS,
SUCH
AS
REIMPLANTATION
OR
REORIENTATION OF THE ANI Monitor V1.
TO MINIMIZE THE RISK OF PATIENT STRANGULATION, THE PATIENT
INTERFACE CABLE MUST BE CAREFULLY PLACED AND SECURED.
DO NOT PLACE THE SKIN ELECTRODES BETWEEN DEFIBRILLATOR PADDLES
WHEN THEY ARE USE ON A PATIENT CONNECTED TO THE ANI Monitor V1.
REUSING A SENSOR ALREADY USED ON ANOTHER PATIENT COULD LEAD TO
CROSS-CONTAMINATION.
IF THE PATIENT DEVELOPS A SKIN REACTION OR OTHER UNUSUAL
SYMPTOMS, REMOVE THE ELECTRODES. IT IS IMPORTANT TO TAKE
PARTICULAR CARE WITH PATIENTS SUFFERING FROM DERMATOLOGICAL
PROBLEMS.
NEVER PUT ELECTRODES ON SKIN INJURIES.
