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ergoline ERS 2 - Revision History; Intended Audience; Stylistic Conventions; Safety Information

ergoline ERS 2
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rEvision History
Revision: 1.0
Date: 2014-04-15
Comments: Applies to software version 1.0 and later
intEndEd audiEnCE
This manual is geared for clinical professionals. Clinical professionals are expected
to have working knowledge of medical procedures, practices, and terminology as
required for completing these examinations.
styListiC ConvEntions
Control keys (soft keys and hard keys) are emphasized by different styles, e.g.,
Start training or [ Create ].
safEty inforMation
General Information
This manual is an integral part of the device. It should be available to the equip-
ment operator at all times. Close observance of the information given in the man-
ual is a prerequisite for proper equipment performance and correct operation and
ensures patient and operator safety. Please note that information pertinent to
several chapters is given only once. Therefore, read the manual once in its entire-
ty. Also observe the information given in the enclosed separate user manuals (e.g.,
the PC and ergometer user manuals).
To ensure maximum patient safety, the specified measuring accuracy, and inter-
ference-free operation, we recommend using only original accessories available
through Ergoline GmbH. The user is responsible if accessories from other manu-
facturers are used.
Ergoline GmbH is responsible for the effects on safety, reliability, and perfor-
mance of the equipment, only if
· assembly operations, extensions, readjustments, modifications, or repairs are
carried out by Ergoline GmbH or persons authorized by Ergoline GmbH
· the device is used in accordance with the instructions given in this manual.
The warranty does not cover damage resulting from the use of unsuitable acces-
sories and consumables from other manufacturers.
Always consult with Ergoline GmbH if you intend to connect equipment not men-
tioned in this manual.
Parts and accessories must comply with the applicable IEC 60601 safety stan-
dards and/or the configured system must comply with the collateral standard IEC
60601-1-1 "Safety requirements for medical electrical systems".

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