CareFusion Diamond-Flex Manual Del Usuario página 5

en
Catalog Numbers
89-6101, 89-6104, 89-6105, 89-6106, 89-6107, 89-6109,
89-6110, 89-6111, 89-6112, 89-6113, 89-6114, 89-6117,
89-6210, 89-6212, 89-6216
Device Components
(a) Actuating Knob with double start thread
(b) Handle
(c) Luer Lock Connector
(d) 05.3mm
(e) Flexible, Segmented Portion
(f) Color Coded Cap for Identification
(g) Protective Sterilizing Sleeve
(h) Actuating Knob Rotated fully counter-clockwise to
completely relax the segmented portion
(i) Luer lock capped
(j) Segments fully relaxed
Indications For Use
Articulating Retractors are designed to retract or elevate organs
and tissue to provide better visualization access to surgical
sites during minimally invasive laparoscopic procedures.
How Supplied
Snowden-Pencer devices are packaged non-sterile. Cleaning
and sterilization must occur prior to use.
Limitations on Reprocessing
Repeated reprocessing has minimal effect on these devices. End
of life is normally determined by wear and damage due to use.
Warnings
Snowden-Pencer devices are to be used in accordance with
these instructions for use. Read all sections of this insert prior
to use. Improper use of the device may cause serious injury. In
addition, improper care and maintenance of the device may
render the device non-sterile prior to patient use and cause a
serious injury to the patient or health care provider.
This device should only be used during insufflator assisted
procedures. This device requires use of high flow insufflation
(15 liters/minute minimum).
Cautions
If there are any variations between these instructions and either
your facility's policies and/or your cleaning/sterilizing equipment
manufacturer's instructions, those variations should be brought
to the attention of the appropriate responsible hospital
personnel for resolution before proceeding with cleaning and
sterilizing your devices.
Use of instrument for a task other than that for which it is
intended will usually result in a damaged or broken device.
Over tightening device actuating knob will result in premature
device failure. Tighten actuating knob until intended shape is
achieved, additional tightening will not improve device
performance.
When sterilizing or storing device, always use protective
sterilizing sleeve provided. Failure to use the sleeve may result
in premature device failure. This device should never be folded
or bent to fit into a small sterilization tray.
Prior to use, inspect device to ensure proper function, insulation
and condition. Do not use devices if they do not satisfactorily
perform their intended function or have physical damage.
Avoid mechanical shock or overstressing devices. Close distal
ends prior to insertion or removal through cannulas.
Only the cleaning and sterilization processes which are defined
within these instructions for use have been validated.
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