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11 Accessories and replacement
parts
A current list of accessories and replacement parts
can be ordered on the internet site of the manufac-
turer or through your authorized specialist dealer.
12 Technical data
Product class to
I
MDR (EU) 2017/745
Dimensions
15 x 3 x 9.2
W x H x D in cm
Weight
0.2 kg
Temperature range
operation
+5 °C to +40 °C
transport and storage
-25 °C to +70 °C
Permitted humidity for operation,
15 % to 93 %, no
transport and storage
condensation
700 hPa -
1060 hPa, corre-
Air pressure range
sponds to an alti-
tude of 3000 m
above MSL
Classification to EN 60601-1-11:
Protection class II
type of protection against electric shock
Classification to DIN EN 60601-1:
operating mode
Continuous duty
Electrical rating
12 V/24 V
Power capacity
2 VA
Insulation of Ethernet port to PC
4 kV
Insulation of Ethernet port to prisma-
1.5 kV
CONNECT module
The right to make design modifications is reserved.
13 Warranty
Löwenstein Medical Technology gives the customer a
limited manufacturer warranty on a new genuine
Löwenstein Medical Technology product and on any
replacement part fitted by Löwenstein Medical
Technology in accordance with the warranty condi-
tions applicable to the product in question and in ac-
cordance with the warranty periods from date of
purchase listed below. The warranty conditions are
available on the website of the manufacturer. We will
also send you the warranty conditions on request.
In the event of a claim under warranty, contact your
specialist dealer.
Product
Warranty
periods
Devices including accessories (except masks)
2 years
Masks including accessories, rechargeable bat-
teries, batteries (unless quoted differently in the
6 months
technical documentation), sensors, patient
circuits
Disposable products
None
14 Declaration of conformity
Löwenstein Medical Technology GmbH + Co. KG,
Kronsaalsweg 40, 22525 Hamburg, Germany, the
manufacturer of the devices described in these In-
structions for Use, hereby declares that the product
complies with the respective regulations of Medical
Devices Directive 93/42/EEC. The unabridged text of
the Declaration of Conformity can be found on the
manufacturer's website.
1
Introduction
1.1 Intended use
The WM090MC module is used to create a link be-
tween approved devices and a PC via Ethernet. It is
also used to create a link between approved devices
and the WM100MP module. The WM090MC module
is designed solely for use indoors. The WM090MC
module is not designed for use in domestic settings.
2
Safety
2.1 Safety information
Risk of injury from device or component
malfunctions!
A damaged device or damaged components may
injure the patient, the user and people in the vicinity.
Only operate the device and its components if
they are externally undamaged.
Only operate the device and its components if a
function check has been completed successfully.
Risk of injury from operating the device outside
the specified ambient conditions!
Using the device outside the specified ambient
conditions may lead to tolerances being exceeded
and to device failure and injury to the patient.
Only operate device within the specified ambient
conditions (see section entitled "Technical data").
Only operate the device in closed rooms.
2.2 General information
•
Connect only the devices and modules permitted
in accordance with these Instructions for Use.
Devices connected to the LAN port of the module
must meet their respective product standard.
Non-medical equipment should be positioned
out of the patient's vicinity.
•
The owner/operator is responsible for ensuring
the compatibility of the therapy device and of all
the components or accessories connected to the
patient before use. Have modifications to the
device carried out only by the manufacturer,
Weinmann, or by specialist staff expressly
authorized by the manufacturer.
•
If the WM090MC module is integrated in an IT
network which includes other devices, the
owner/operator must check whether this causes
risks to patients, operators or third parties
(IEC 80001-1).
•
The use of third-party articles may lead to
incompatibility with the device. In such cases,
please be aware that any claim under warranty
and liability will be void if neither the accessories
nor the genuine replacement parts
recommended in the Instructions for Use are
used.
•
To prevent infection or bacterial contamination,
follow the section about hygiene treatment (see
section entitled "Hygiene treatment").
•
In the EU: As a user and/or patient, you must
report any severe adverse events occurring in
connection with the product to the manufacturer
and to the responsible authorities.
3
Product description
3.1 Overview
A diagram of the individual parts can be found on the
title page.
Key
1. Connection for prismaPSG (WM100MP)
2. LAN port for connecting to a PC.
3. Port for prisma SMART series (WM090TD)
4. PSG port to the prismaCONNECT module
(WM100MC).
5. LAN port to the prismaCONNECT module
(WM100MC).
6. Update LED - indicates an update in progress.
7. Error LED - indicates a fault.
8. PSG key - outputs test signals to the prismaPSG.
3.2 Ferrite
Ferrite (see Figure 1 and Figure 2) is a non-conduc-
tive material which absorbs electromagnetic waves
passing through it. It serves as an interference filter
which eliminates electromagnetic waves before they
can be emitted via the cable.
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