Trio™ Operating Instructions
0070-10-0666-01
xi
Notes
Introduction
Notes
NOTE:
Potential hazards due to errors in software or hardware
have been minimized by actions taken in accordance with
IEC 60601-1.
NOTE:
Messages are provided to assist in the identification and
correction of problems that may occur with the monitor.
NOTE:
Should the device become accidently saturated with any
liquid, immediately discontinue use and contact Customer
Service.
NOTE:
The comparison testing conducted via the auscultatory
method used both Phase 4 and Phase 5 Korotkoff sounds.
Reports of study findings for both the auscultatory method
as well as the intra-arterial methods are available by
contacting Technical Support (201) 995-8116.
NOTE:
Only operate this device within the specified operating
signal range.
Indication For Use
The
Trio
™
monitor is intended for use in healthcare settings under the direct supervision of a
licensed healthcare practitioner. The intended use of the monitor is to monitor physiologic
parameter data on adult and pediatric patients. Physiologic data includes:
electrocardiogram, invasive blood pressure, non-invasive blood pressure (NIBP), pulse
oximetry, heart rate (derived from ECG, SpO
2
, or NIBP), respiration and temperature as
summarized in the operating instructions manual. The information can be displayed, stored,
trended and printed.
The monitor is not intended for home use. The monitor is not intended to be an apnea
monitor. It was not designed or validated for use as an apnea monitor.
Unpacking
Remove the instrument and accessories from the shipping cartons and examine them for signs
of shipping damage. Save all packing materials, invoice and bill of lading. These may be
required to process a claim with the carrier. Check all materials against the packing list.
Contact your Sales Representative or Distributor for assistance in resolving shipping
problems.