ANI Monitor V1 - Continuous analgesia monitoring system
5
MD/PRD/IN16.ANIV1 V.14 - 12 MAR 2020
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 V1, 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
V1
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