ANI Monitor V2 - Continuous analgesia monitoring system
MD/PRD/IN16.ANIV2 v.07 - 12 MAR 2020
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DO NOT PLACE THE SKIN ELECTRODES BETWEEN DEFIBRILLATOR PADDLES
WHEN THEY ARE USE ON A PATIENT CONNECTED TO THE ANI Monitor V2.
ELECTRICAL SHOCK:
- 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.
- THE MANUFACTURER'S INSPECTION OF THIS APPARATUS VERIFIED THAT THE
GROUND LEAKAGE CURRENT AND THE PATIENT SAFETY CURRENT WERE BELOW
THE LIMITS SPECIFIED BY THE APPLICABLE SAFETY STANDARDS. AS A MATTER
OF SAFE PRACTICE, THE FACILITY MUST CONDUCT TESTS TO VERIFY THESE
CURRENTS ESPECIALLY WHEN A BIOMEDICAL ENGINEERING TECHNICIAN
PERIODICALLY PERFORMS MAINTENANCE.
WHENEVER AN EVENT SUCH AS SPILLAGE OF BLOOD OR LIQUIDS OCCURS ON
THE ANI Monitor V2, RE-TEST GROUND LEAKAGE CURRENT BEFORE FURTHER
USE.
OBSERVE UNIVERSAL PRECAUTIONS TO PREVENT CONTACT WITH BLOOD OR
OTHER POTENTIALLY INFECTIOUS MATERIALS. CONTAMINATED MATERIALS MUST
BE HANDLED IN ACCORDANCE WITH THE FACILITY'S APPLICABLE HEALTH AND
SAFETY REGULATIONS.
DO NOT MIX DISINFECTING SOLUTIONS (e.g., BLEACH AND AMMONIA), AS TOXIC
GASES MAY RESULT.
THE ANI Monitor V2 COMPLIES WITH THE ELECTROMAGNETIC COMPATIBILITY
REQUIREMENTS OF EN 60601-1-2. OPERATION OF THIS DEVICE MAY AFFECT OR BE
AFFECTED BY OTHER EQUIPMENT IN THE VICINITY DUE TO ELECTROMAGNETIC
INTERFERENCE (EMI). IF THIS OCCURS:
- INCREASE SEPARATION BETWEEN DEVICES
- CHANGE THE ORIENTATION OF DEVICE CABLING
- PLUG DEVICES INTO SEPARATE OUTLETS
- CONTACT YOUR MDOLORIS MEDICAL SYSTEMS REPRESENTATIVE.
