User Manual: xr50+_eng
5
Cardioline S.p.A.
Via Linz,151
38121 Trento (TN)
www.cardioline.com
Sales office:
Via F.lli Bronzetti, 8 20129 Milano (MI) Italy tel.+39 02 94750470
fax +39 02 94750471
xr50+
1 General Information
• The product xr50+ bears the CE marking CE‑0123
(Notified Body: TÜV), indicating its compliance with the
provisions of the Council Directive 93/42/EEC about
medical devices and fulfills the essential requirements
of Annex I of this directive.
The CE marking covers only the accessories listed in the
Order Information chapter. The device is an MDD class
IIa product.
• The device fulfills the requirements of the standard
EN 60601‑1 "Medical electrical equipment, Part 1:
General Requirements for Safety" as well as the inter‑
ference protection requirements of standard EN 60601‑1‑2
"Electromagnetic Compatibility – Medical Electrical
Devices".
The radio‑interference emitted by this product is within
the limits specified in EN 55011, class B.
• The symbol
means: protection class II.
• This manual is an integral part of the device. It should
be available to the device operator at all times. Close
observance of the information given in the manual is a
prerequisite for proper device performance and correct
operation and ensures patient and operator safety.
Please note that information pertinent to several chap‑
ters is given only once. Therefore, read the manual once
in its entirety.
• The symbols
mean:
Consult accompanying documents.
They indicate points that are of particular importance in
the operation of the device.
• Observance of the safety information protects from
injuries and prevents inappropriate use of the device.
All device users and persons responsible for assembly,
maintenance, inspection and repair of the device must
read and understand the content of this manual, before
using the device or working with it. Paragraphs with
special symbols are of particular importance.
• If unauthorized individuals open the control terminal,
damaging the calibration sticker, any warranty claim
shall become void.
• This manual reflects the device specifications and appli‑
cable safety standards valid at the time of printing.
All rights are reserved for devices, circuits, techniques,
software programs, and names appearing in this manual.
• On request
ergoline
will provide a Field Service Manual.
• The
ergoline
quality management system complies with
the standard EN ISO 13485: 2016.
• The safety information given in this manual is classified
as follows:
Danger
indicates an imminent hazard. If not avoided, the hazard will
result in death or serious injury.
Warning
indicates a hazard. If not avoided, the hazard may result in
minor injury and/or product/property damage.
Caution
Indicates a potential hazard. If not avoided, the hazard may
result in minor injury and/or product/property damage.
• To ensure patient safety, the specified measuring accu‑
racy, and interference‑free operation, we recommend
using only original
ergoline
accessories. The user is
responsible if accessories from other manufacturers are
used.
•
ergoline
is responsible for the safety, reliability, and
performance of the device, only if
— modifications and repair are carried out by ergoline
GmbH or by an organization expressly authorized
by ergoline GmbH
— the device is used in accordance with the instruc‑
tions given in this operator manual.
