Table Des Matières; Safety Instructions; Intended Use; Receiving/Inspection - Ohio Medical 6730-0350-800 Mode D'emploi

Table of Contents
Safety Instructions ............................................................2
Intended use ......................................................................2
Receiving/Inspection ........................................................2
User Responsibility ..........................................................2
Definitions .........................................................................3
Venturi/ejector suction module identification ................4
Equipment Set Up .............................................................4
Pre-use Checkout Procedure ...........................................5
Cleaning .............................................................................6
Troubleshooting ................................................................6
Warranty .............................................................................7

Safety Instructions

This manual provides you with important information about the Venturi/Ejector Suction Module.
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 venturi/ ejector suction module is an accessory designed to generate a vacuum supply
through the use of pressurized medical air or oxygen. It is not a stand alone medical device. It
should always be used with a vacuum regulator. The device is to be used with Ohio Medical
vacuum regulators only.
Receiving / Inspection:
Remove product from package and inspect for damage. If product is damaged, DO NOT USE and
contact your dealer or equipment provider.

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 done
in strict accordance to the written instructions provided by Ohio Medical. If this device is subject to
improper maintenance, repair, use and/or abuse leading to malfunction of the device, replacement
is the sole responsibility of the user.
123 A This alpha character indicates the year of product manufacture and when the serial
number was assigned; "Y" = 1995, "Z" = 1996,
"A" = 1997, etc. "I" and "O" are not used.
WARNINGS This device is to be used only by persons who have been adequately
⚠
instructed in its use.
2
6700-0382-000 (Rev. 7) 08/2020