
Ultra Cart Technical Manual 3 2/8/2013
GD-99021 Rev. E
User/Patient Safety
WARNINGS:
DO NOT apply High Flow suction or allow extended
exposure of suction to the tissue associated with
procedures that require either no suction, low vacuum or
low flow suction, for example, passive chest drainage.
ALWAYS consider the type of tissue associated with the
surgical procedure BEFORE using this system. Failure to
comply may result in severe injury or death.
Before using this system, read and understand the information in
this manual. Suction equipment should only be used by people
that have had adequate training on the use of this type of
equipment. Pay special attention to WARNING information.
Become familiar with the system components prior to use.
The health care professional performing any procedure is
responsible for determining the appropriateness of this
equipment and the specific technique used for each patient.
Dornoch Medical Systems, Inc., as a manufacturer, does not
recommend surgical procedure or technique.
DO NOT use this system outside the scope of the defined
indications for use.
DO NOT use this system for applications that require a
constant vacuum level.
The reservoir scale and fluid volume display are not diagnostic
tools. DO NOT use the scale or volume display to accurately
calculate the amount of fluid loss from the patient.
Upon initial receipt and before each use, operate the equipment
and inspect each component for damage. DO NOT use any
component if damage is apparent.
ALWAYS close all unused ports and remove all unused tubing
to maintain optimal suction levels. The suction levels of each
canister are interdependent and linked to a common vacuum
source. Failure to comply may result in the unexpected reduction
of suction and patient injury.
The suction level of this product relative to its vacuum limit
setting may fluctuate significantly but will not exceed its limit.
DO NOT use this system if vacuum fluctuation may cause
patient injury. ALWAYS consider the type of surgical procedure
before using this system.
ALWAYS follow current local regulations governing procedure-
specific suction levels to remove fluid waste safely from a
surgical site.
Reservoirs are for surgical and bodily fluid collection only; do
not place any items into the reservoir for disposal. Caustic or
other harmful chemicals may harm the equipment and will void
the warranty.
Handling biohazard waste is potentially dangerous. ALWAYS
follow current local regulations governing biohazard waste to
safely handle and dispose of surgical fluid waste.
Manifolds and suction tubing may contain surgical waste after
use. ALWAYS handle these disposable accessories as
“potentially infectious materials” after use. ALWAYS wear
gloves and protective eye wear when removing and disposing of
these disposable accessories.
The Blood-borne Pathogens Standards, provided by the
Occupational Safety and Health Association (OSHA), requires
that all workers, having exposure to “potentially infectious
materials”, should wear the correct personal protection
equipment.
To avoid the risk of electrical shock, this equipment must be
connected to electrical outlet with a protective earth ground.
Verify all access doors are securely in place before operating this
unit.
ALWAYS follow reservoir overfill alarms to prevent overfill.
Use only Dornoch Medical Systems, Inc. approved accessories.
Do not connect items to this system that are not designed for or
specified for use with this system.
ALWAYS have more than one person unpack and lift the
equipment off the shipping pallet.
Perform recommended maintenance as indicated in these
instructions. Only trained and experienced health care
professionals should maintain this equipment.
No user serviceable parts inside the unit. Contact Dornoch
Medical Systems, Inc. customer service if an issue arises. Only
authorized service personnel should open any of the access
covers on this equipment. User operation does not require
access to these areas.
The unit is for use within the hospital and/or surgery center.
The unit is moveable but is not intended to be transportable or
used in the outside environment. To be used within the
healthcare facility ONLY.
DO NOT use the system with patients that are being treated
with radioisotopes or hazardous chemotherapy agents.
ALWAYS use the handle to move the cart. DO NOT push or
pull the cart by grasping any other part of the outer surface.
NEVER hang any heavy object from the cart handles.
No incline planes of operation.
ALWAYS follow reservoir overfill alarms to prevent overfill.
DO NOT use the system if leakage of surgical fluid waste
occurs. Disconnect power immediately and call Dornoch
Medical Systems, Inc. Customer Service.
DO NOT allow fluid of any kind to spill directly onto the
exterior surface of the electrically-powered cart.
DO NOT use the cart until it has been tested properly and the
Evac Unit has been installed and tested properly.
This unit uses both bleach and enzyme in its operation. When
replacing bottles, always wear the appropriate Personal
Protective Equipment. Use only Dornoch Medical Systems, Inc.
approved Bleach and Enzyme to avoid damage to the system
components.
This equipment is not suitable for use in the presence of
flammable anesthetic mixtures with air, oxygen or nitrous oxide.
Is not intended for use with AP or APG equipment.
Hot Water Temperatures higher than 118 0F can cause damage
to the unit.
There are no known significant risks of reciprocal interference
posed by the presence of this equipment or its operation in
either the operating room suites or other areas when used during
specific investigations and/or treatments.
There are no known potential electromagnetic or other
interferences between this unit and other devices located and/or
operated within the area of the operating room suites.