Barco MUIP-2213 handleiding
Handleiding
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25R5916765 /01 MUIP-2213
Decommissioning is the process of disposing a device, or removing a device from its originally intended use in
the health care facility to an alternative use.
Every health care facility or institution shall have standard operating procedures in place to decommission a
device according to the Occupational Safety and Health Administration (OSHA) regulations or/and the World
Health Organization (WHO) Decommissioning Medical Devices Technical guideline.
The seller / manufacturer of the device has no legal obligation on the device sold in the event that the health
care facility or institution decides to activate the decommissioning process.
Overview
The structure and the specifications of this device as well as the materials used for manufacturing makes it
easy to wipe and clean and therefore suitable to be used for various applications in hospitals and other
medical environments, where procedures for frequent cleaning are specified.
However, normal use shall exclude biological contaminated environments, to prevent spreading of infections.
Therefore use of this device in such environments is at the exclusive risk of Customer. In case this device is
used where potential biological contamination cannot be excluded.
Customer shall implement the decontamination process as defined in the latest edition of the ANSI/AAMI
ST35 standard on each single failed Product that is returned for servicing, repair, reworking or failure
investigation to Seller (or to the Authorized Service Provider). At least one adhesive yellow label shall be
attached on the top site of the package of returned Product and accompanied by a declaration statement
proving the Product has been successfully decontaminated.
Returned Products that are not provided with such external decontamination label, and/or whenever such
declaration is missing, can be rejected by Seller (or by the Authorized Service Provider) and shipped back at
Customer expenses.
4.5 Regulatory information
Intended Purpose
MUIP-2213 is a LCD user interface for use in the hospital environment. It can be used for third party software
applications that provide a user interface for medical systems. The equipment can be used in CathLab
Examination Rooms & Control Rooms, Surgical Rooms and Hybrid Operating Rooms, both inside and outside
the patient area. The equipment is not intended to be used for displaying medical images, nor for diagnostic
purposes.
Factory address
Fimi S.r.l., Via Saul Banfi 1, 21047 Saronno, VA, Italy
Manufacturing country
The manufacturing country of the product is indicated on the product label (“Made in …”).
Importers contact information
To find your local importer, contact one of Barco’s regional offices via the contact information provided on our
website (www.barco.com).
FCC class B
This device complies with Part 15 of the FCC Rules. Operation is subject to the following two conditions: (1)
this device may not cause harmful interference, and (2) this device must accept any interference received,
including interference that may cause undesired operation.
This device has been tested and found to comply with the limits for a Class B digital device, pursuant to Part
15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference
in a residential installation. This device generates, uses and can radiate radio frequency energy and, if not
installed and used in accordance with the instructions, may cause harmful interference to radio
communications. However, there is no guarantee that interference will not occur in a particular installation. If
this device does cause harmful interference to radio or television reception, which can be determined by
Important information
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Productinformatie
| Merk | Barco |
| Model | MUIP-2213 |
| Categorie | Niet gecategoriseerd |
| Taal | Nederlands |
| Grootte | 3833 MB |
