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AGFA ID Tablet Getting Started page 2

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without appropriate qualification and training
as well as using unapproved spare parts may
lead to serious risk of injury and damage to
the equipment as well as making the
warranty void.
7
Cleaning and Disinfection
All appropriate policies and procedures should be
followed to avoid contamination of the staff, patients and
the ID Tablet. All existing universal precautions should be
taken to avoid that the ID Tablet comes into contact with
potential contaminations.
To clean the exterior of the ID Tablet
Unplug the ID Tablet from the PC.
Wipe the exterior of the ID Tablet with a clean, soft,
damp cloth. Use a mild soap or detergent if required but
never use ammonia based cleaner.
Plug the ID Tablet back into the PC.
8
Labels
The identification label is located at the back side of the
ID Tablet.
9
Technical specifications
Power supply
5V DC via USB interface
Class III (IEC60950 /
Classification
UL60950)
2287B EN 20191031
Operating conditions:
Temp.:
5 to 40°C
RH:
5% to 85%
12 kg
Weight:
Dimensions H x W x D:
115 x 390 x 450 mm
Maximum power
200 mA
consumption:
The equipment is suited for continuous operation.
The ID Tablet is provided with 1 USB 2.0 interface to
connect it to the PC for data transmission and power
supply.
10
System Documentation
For general safety directions, refer to the user
documentation of the Agfa CR system.
11
Environmental Protection
WEEE end user information
(Applicable in the European Union and other European
countries with separate collection system)
This symbol on the product, or in the manual and in the
warranty, and/or on its packaging indicates that this
product shall not be treated as household waste.
For more detailed information about take-back and
recycling of this product, please contact your local Agfa
service organization. By ensuring this product is disposed
of correctly, you will help prevent potential negative
consequences for the environment and human health,
Getting started with the ID Tablet
which could otherwise be caused by inappropriate waste
handling of this product. The recycling of materials will
help to conserve natural resources.
12
Compliance
For general safety directions, refer to the user
documentation of the Agfa CR system.
Both the workstation console and the ID Tablet comply
with the following safety standards:
UL 60950 / EN 60950 / EN 62368
CAN/CSA 22.2 NO. 60950-1-07, Third Edition (TÜV- NRTL
c-us)
The equipment bears the CE mark and fully
complies with European Regulation (EU)
2017/745 on medical devices (MDR).and with
the federal code of the United States, bearing on:
Emission and immunity according to EN 60601-1-2, for
emissions the equipment complies with EN 55011 class A
(CISPR 11). This is a Class A product. In a domestic
environment this product may cause radio interference in
which case the user may be required to take adequate
measures.
Emissions according to 47 CFR part 15 subpart B, Class A.
This equipment has been tested and found to comply with
the limits for a Class A digital device, pursuant to part 15
of the FCC rules. These limits are designed to provide
reasonable protection against harmful interference when
the equipment is operated in a commercial environment.
This equipment generates, uses, and can radiate radio
frequency energy and, if not installed and used in
accordance with the Instruction manual, may cause
harmful interference to radio communications. Operation
of this equipment in a residential area is likely to cause
harmful interference in which case the user will be
required to correct the interference at his own expense.
Radio-parameters according to ETS 300330.
Agfa NV, Septestraat 27, B-2640 Mortsel, Belgium

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