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Weinmann MEDUCORE Standard2 User Manual

Weinmann MEDUCORE Standard2
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WM 68401 04/2021
MEDUCORE Standard
2
EN 33
2 Safety
Delay in treatment due to power supply network disruption!
Disruptions to the power supply network may cause visible
disruptions to the ECG. This may lead to incorrect measurement
results and alarms and in AED mode, lead to shock delivery at the
wrong time. This may delay therapy and injure the patient.
If there is major disruption to the power supply network, only
operate the device with a battery.
2.7 General instructions
If third-party items are used, functional failures and restricted
fitness for use may result. Biocompatibility requirements may
also not be met. Please note that in such cases, any warranty
claim and liability will be voided if neither the accessories
recommended in the instructions for use nor original
replacement parts are used. Third-party items may increase
radiation output or reduce interference immunity.
The manufacturer, WEINMANN Emergency, guarantees the
compatibility of the device and of all components or
accessories connected to the patient prior to the session. Have
modifications to the device or accessories (exception: software
update) carried out only by the manufacturer,
WEINMANN Emergency, or by a technician expressly
authorized by it. Do not use any articles from third parties.
Follow the section on hygienic reprocessing in order to avoid
infection or bacterial contamination (see “8 Hygienic
reprocessing”, page 230).
As the user, always stay in the immediate vicinity of the device
and the patient.
Risks due to software errors have been minimized by means of
extensive qualification measures.
This device’s software contains code which is subject to the
General Public License (GPL). We will send you the source code
and the GPL on request.

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Weinmann MEDUCORE Standard2 Specifications

General IconGeneral
BrandWeinmann
ModelMEDUCORE Standard2
CategoryMedical Equipment
LanguageEnglish

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