Dräger Fabius plus XL User Manual

Technical data
42 Supplement Fabius plus XL SW 3.n
EMC declaration
The following chapters have changed:
General information
This device was tested for electromagnetic
compatibility using accessories from the list of
accessories. Other accessories may only be used
if they do not compromise the electromagnetic
compatibility. The use of non-compliant
accessories may result in increased
electromagnetic emissions or decreased
electromagnetic immunity of the device.
This device may be used in the direct vicinity of
other devices only if Dräger has approved this
device arrangement. If no approval has been given
by Dräger, it must be ensured that this device
functions correctly in the desired arrangement
before use. The instructions for use for the other
devices must be followed.
Electromagnetic emissions
The chapter has been deleted.
Electromagnetic environment
This device may only be used in environments
specified in the instructions for use under
"Environments of use" in the chapter "Application".
Emissions Compliance
Radiated emis-
sions
Class A, group 1 (30 MHz to
1GHz)
Conducted emis-
sions
Class A, group 1 (150 kHz to
30 MHz)
NOTE
The emissions characteristics of this equipment
make it suitable for use in industrial areas and
hospitals (CISPR 11 class A). If it is used in a
residential environment (for which CISPR 11
class B is normally required), this equipment
might not offer adequate protection to radio-
frequency communication services.
The user might need to take mitigation
measures, such as relocating or re-orienting the
equipment.

Dräger Fabius plus XL Specifications

General

Brand	Dräger
Model	Fabius plus XL
Category	Medical Equipment
Language	English