Dräger SilverLine Instrucciones De Uso página 35

Abbreviations
Abbreviation Explanation
Air Medical compressed air
O Oxygen
2
N O Nitrous oxide
2
CO Carbon dioxide
2
p2 Output pressure
p1, p3 Input pressure
Q1 Nominal flow
STPD Standard temperature and pressure,
dry, at 20 °C (68 °F), 1013 hPa
(14.7 psi), dry gas
For your safety and that of your
patients
General safety information
Strictly follow these instructions for use
WARNING
Risk of incorrect operation and of incorrect use
Any use of the medical device requires full un-
derstanding and strict observation of all sec-
tions of these instructions for use. The medical
device may only be used for the purpose spec-
ified under Intended use.
Strictly observe all WARNING and CAUTION
statements throughout these instructions for
use and all statements on medical device la-
bels. Failure to observe these safety informa-
tion statements constitutes a use of the medi-
cal device that is inconsistent with its intended
use.
Instructions for use SilverLine
Maintenance
WARNING
Risk if service is not performed regularly
If service is not performed regularly, malfunc-
tions may occur, which can result in personal
injury and property damage.
Perform the service in accordance with the
chapter "Service".
Accessories
WARNING
Risk due to incompatible accessories
Dräger has tested only the compatibility of ac-
cessories listed in the current list of accesso-
ries. If other, incompatible accessories are
used, there is a risk of patient injury due to
medical device failure.
Dräger recommends that the medical device is
only used together with accessories listed in
the current list of accessories.
WARNING
Risk of malfunctions
Installation to the main device must be in ac-
cordance with the instructions for use for the
main device to which this medical device is be-
ing connected. Check that connection is secure
with the main device system.
CAUTION
Risk of contamination and soiling
To avoid contamination and soiling, keep the medi-
cal device in its packaging until use. Do not use the
medical device if the primary packaging is dama-
ged.
Patient safety
The design of the medical device, the accompanying
documentation, and the labeling on the medical de-
vice are based on the assumption that the purchase
and the use of the medical device are restricted to
persons familiar with the most important inherent
characteristics of the medical device.
Instructions and WARNING and CAUTION state-
ments are therefore largely limited to the specifics of
the Dräger medical device.
The instructions for use do not contain any informa-
tion on the following points:
– Risks that are obvious to users
– Consequences of obvious improper use of the
medical device
– Potentially negative effects on patients with dif-
ferent underlying diseases
Medical device modification or misuse can be dan-
gerous.
Mandatory reporting of adverse events
Serious adverse events with this product must be re-
ported to Dräger and the responsible authorities.
Product-specific safety information
WARNING
Risk of malfunctions and of patient injury
Modifications may damage the device or impair
the proper functioning of the device and lead to
patient injury.
Do not modify or misuse the pressure reducer.
Do not remove the inlet filter.
English US
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