Table Des Matières; Safety Instructions; Intended Use; Receiving/Inspection - Ohio Medical ISU Rx Only Mode D'emploi

Régulateur d'aspiration, unité d'aspiration intermittente
Table des Matières

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  • FRANÇAIS, page 21
Table of Contents
Safety Instructions ............................................................. 2
Intended use ..................................................................... 2
Receiving/Inspection ......................................................... 2
User Responsibility ........................................................... 2
Definitions/Abbreviations ................................................... 3
Regulator Identification...................................................... 4
Operation .......................................................................... 4
Cleaning ............................................................................ 9
Troubleshooting ................................................................. 9
Warranty .......................................................................... 10

Safety Instructions

This manual provides you with important information about the Intermittent
Suction Unit (ISU). To ensure the safe and proper use of this device, READ
and UNDERSTAND all of the safety and operating instructions. IF YOU DO
NOT UNDERSTAND THESE INSTRUCTIONS, OR HAVE ANY QUESTIONS,
CONTACT YOUR SUPERVISOR, DEALER OR THE MANUFACTURER BEFORE
ATTEMPTING TO USE THE DEVICE.

Intended Use:

The vacuum regulator is intended to be used in the medical facility as a means to
evacuate media (i.e. fluids) from the body.
Receiving / Inspection:
Remove product from package and inspect for damage. If product is damaged, DO
NOT USE and contact your dealer or equipment provider.
WARNINGS
This device is to be used only by persons who have been adequately
instructed in its use.
Do not use this device in the presence of flammable anesthetics. Static
charges my not dissipate and a possible explosion hazard exists in the
presence of these agents.

User Responsibility

This product performs as explained in this manual as long as the assembly, use,
repair and maintenance are properly followed according to our instructions. Periodic
review of this device is recommended. If any damage or defects are present,
the product should not be used. This includes parts that may have been altered,
contaminated, worn or missing. If any of the above are noted, immediate repair /
replacement is required. In compliance with the Ohio Medical Warranty, repair of
this device is not to be performed by anyone other than a qualified professional and
2
6700-0359-000
(Rev. 9) 08/2020

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