Dräger Atlan A100 Instructions For Use Manual page 306

Anesthesia workstation
Hide thumbs Also See for Atlan A100:
Table of Contents

Advertisement

Technical data
15.26.4
USB
Functionality
This device supports the following interfaces based on USB 2.0:
– USB mass storage devices
The USB port supports data transmission to external storage media. Existing data
on external storage media may be deleted during this process.
The following data is transmitted to the USB mass storage device over the interface
unencrypted:
– Logbook with details on weight and height of the patient
– Screenshots with screen contents
The following functions can be performed if no patient is connected to the device:
– Exporting and importing device configurations
– Installing software options
Required properties
Only devices that are included in the list of accessories or which correspond to the
"mass storage medium" USB device class may be connected. For example, no
provision has been made for connecting devices whose battery is to be charged.
Dräger recommends the use of storage media with hardware encryption.
USB mass storage devices must be checked for malware and approved before
being connected to the device. Checking and approval must be performed by the IT
administrator or equipment officer of the health-care facility in accordance with the
specifications of the health-care facility.
The following USB devices must not be connected:
– Active USB devices (own power supply)
– Devices that use wireless technology
– Cellular phones
15.26.5
RFID
Functionality
This medical device may be equipped with an RFID module (Radio Frequency
Identification) to enable wireless communication with Infinity ID accessories.
This medical device has been designed and manufactured to comply with emission
limit values for high-frequency energy. These limit values are part of international
safety standards, such as IEC 60601-1-2, and standards on radio devices, such as
EN 300330, and have been specified by the authorities.
Changes and modifications that have not been expressly approved by Dräger can
mean that the user is no longer permitted to operate the device.
Dräger hereby declares that this medical device, including the radio devices,
complies with Directive 2014/53/EU. The full EU declaration of conformity can be
found at the following website: http://www.draeger.com/doc-radio
306
|
Instructions for use
Atlan A100 (XL), A300 (XL), A350 (XL) SW 2.1n

Advertisement

Table of Contents
loading

Table of Contents