Overview Of Alarms; Warranty; Return And Disposal; Provider's Notes - Drive DeVilbiss 1025 Serie Guía De Instrucciones

OVERVIEW OF ALARMS

This device contains an alarm system which monitors the state of the device and alerts of abnormal operation, loss of essential performance or failures . Alarm conditions are
shown on the LED display . The alarm system functions are tested at power up by lighting all visual alarm indicators and sounding the audible alarm (beep) .
All alarms are Low Priority Technical Alarms .
Alarm Condition LED Indicator
Start-up Period
Low Oxygen
Concentration
Malfunction

WARRANTY

DeVilbiss provides warranty for this device . Use only DeVilbiss approved original spare parts for maintenance and repair to retain warranty . Using unapproved or non-original
spare parts would void warranty .

RETURN AND DISPOSAL

This device may not be disposed of with household waste . After use of the device, please return the device to the provider for disposal . This device contains electrical and/or
electronic components that must be recycled per EU Directive 2012/19/EU-Waste Electrical and Electronic Equipment (WEEE) . Non-infectious used accessories (e .g . nasal
cannula) can be disposed of as residential waste . The disposal of infectious accessories (e .g . nasal cannula from an infected user) must be made via an approved waste
disposal company . Names and addresses can be obtained from the local municipality .
PROVIDER'S NOTES - Cleaning and Disinfection When There is a Patient Change
When medical devices have already been used with a patient, contamination with human pathogenic germs should be assumed (unless there is evidence to the contrary) . The
next patient, user or third party should be protected by appropriate handling and preparation .
Therefore, when there is a patient change, people must be protected during the transport and handling of the device, and the device must be fully processed, i .e ., cleaned and
disinfected, by suitably trained personnel before reuse to protect the next patient. The complete processing may only be done by the manufacturer or by a qualified DeVilbiss
provider/service technician .
NOTE– If the following described complete processing of the concentrator by a qualified DeVilbiss provider/technician is not possible, the device must not be used by another
patient!
DeVilbiss Healthcare recommends that at least the following procedures be carried out by the manufacturer or a qualified third party between uses by different patients.
NOTE– If preventive maintenance is due at this time, these procedures should be carried out in addition to the servicing procedures.
1. Dispose of all accessory components that are not suitable for reuse, i.e., particularly the oxygen tubing, the nasal cannula/mask, oxygen outlet connector and humidifier
bottle .
The concentrator must be disconnected from the power supply for this step: Open the concentrator and remove all dust deposits inside the cabinet with an
2 .
appropriate vacuum cleaner .
3 . Clean and disinfect all parts of the cabinet inside and outside and the power cord with a suitable disinfecting agent, e .g ., Microbac Forte or Terralin® .
4 . Check the cord, the plug on the back of the device, the power switch, the fuse holder and the indicator light for possible damage .
5 . Replace all damaged or worn components .
6. Replace the cabinet air filter on the back of the device.
7. Check the oxygen concentration. If the device is within specifications, the extended life intake bacteria filter does not need to be replaced between patients. If the
concentration is not within specifications, the provider should refer to the service manual section on Troubleshooting.
NOTE– There is no portion of the gas pathways through the concentrator that could be contaminated with body fluids under normal conditions.
The device patient connection may unintentionally become contaminated with expired gases for a single fault condition i .e ., a hose internal to the device becomes
disconnected. This condition will cause no flow out of the device and/or an alarm condition. Should this occur refer to the Service Manual for additional instructions.
Disinfection
WARNING
Electric shock hazard. Do not attempt to open or remove cabinet. There are no user-serviceable internal components.
NOTE– The disinfection process can only be completed by the manufacturer or by a qualified DeVilbiss provider/service technician.
Cabinet parts, inside and out, power cord Between patients
Oxygen Tubing, nasal cannula, Oxygen
outlet connector, humidifier bottle
Inside cabinet
A-1025
Visual Alarm Signal
Meaning
YELLOW
Low O LED ON
2
YELLOW
Low O LED ON when O is
2 2
<87%
RED
Service Required LED ON
Recommended disinfection
interval
Do not clean, replace between patients
Between patients
Visual Alarm Signal
Audible Alarm Signal
No
Yes
Before O drops below 82%
2
Yes
Number of disinfection
cycles *
20
N/A
N/A
Action to take
Cleared by
Wait for unit to finish startup
After startup period, O
2
period, up to 15 minutes
reaches at least 87%
Turn unit off See Troubleshooting table
Return unit to provider for
Turn unit off
Compatible disinfection method
Microbac Forte, Terralin
OPA or Peract,1:10 chlorine bleach
(5 .25%) and water solution
N/A
Remove dust with a vacuum cleaner
service
, Aldahol, Cidex
®
EN - 9