DeVilbiss Healthcare 515A Series Manual

0044
EN
DeVilbiss® Oxygen Concentrator
Instruction Guide
WARNING–Read instruction guide before operating this equipment.
CAUTION– Federal (U.S.A.) law restricts this device to sale by or on the order
of a physician.
MADE IN THE USA of U.S. and Imported Parts
DANGER–NO SMOKING
ES
Guía de Instrucciones del Concentrador
de Oxígeno DeVilbiss®
ADVERTENCIA–Lea la guía de instrucciones antes de poner a funcionar
este equipo.
PRECAUCION– La ley federal (EE.UU.) establece que este aparato sólo lo
puede vender un médico o por prescripción del mismo.
FABRICADO EN EE. UU. de partes nacionales e importadas
PELIGRO–NO FUMAR
FR
Guide d’Instructions sur le Concentrateur
d’oxygène de DeVilbiss®
AVERTISSEMENT–Lire le mode d’emploi avant d’utiliser ce dispositif.
ATTENTION–En vertu de la Loi fédérale américaine, la vente de cet appareil
n’est autorisée que par un médecin ou sur ordonnance de ce dernier.
FABRIQUÉ AUX ÉTATS-UNIS avec des pièces des États-Unis et des pièces
importées
DANGER–NE PAS FUMER
DE
DeVilbiss® Sauerstoffkonzentrator
Bedienungsanleitung
WARNUNG–Vor Inbetriebnahme des Gerätes Bedienungshinweise lesen.
ACHTUNG– Dieses Gerät darf US-Bundesgesetzen zufolge nur von Ärzten
oder auf deren Anweisung hin verkauft werden.
Gefertigt in den USA unter Verwendung amerikanischer und importierter Teile.
GEFAHR–RAUCHEN VERBOTEN
IT
Manuale di Istruzioni del Concentratore di
ossigeno DeVilbiss®
AVVERTENZA–Leggere il manuale di istruzioni prima di usarel’apparecchio
ATTENZIONE–La legislazione federale degli Stati Uniti limita la vendita di
questo prodotto al personale medico o alle persone munite di prescrizione
medica.
ASSEMBLATO NEGLI USA con componenti prodotti negli Stati Uniti e importati.
PERICOLO - NON FUMARE
NL
DeVilbiss® zuurstofconcentrator
Instructiehandboekje
WAARSCHUWING–Lees dit instructiehandboekje zorgvuldig door voordat
u het apparaat gaat gebruiken.
ATTENTIE–De federale wetgebing in de Verenigde Staten schrijft voor dat
dit apparaat uitsluitend mag worden verkocht of voorgeschreven door een
arts.
GEPRODUCEERD IN DE VERENIGDE STATEN met Amerikaanse en
geïmporteerde onderdelen
GEVAAR– VERBODEN TE ROKEN
515A & 515 Series
Serie de 515A & 515
Série 515A & 515
515A & 515 Serie
Serie da 515A & 515
515A & 515 Serie

2
00
55
LPM O2
44
33
22
11
Increase
DeVilbiss 4- & 5-Liter Series
EN ENGLISH.................................................................................................................................................................................... EN-2
ES ESPAÑOL ................................................................................................................................................................................... ES-10
FR FRANÇAIS.................................................................................................................................................................................. FR-18
DE DEUTSCH................................................................................................................................................................................... DE-26
IT ITALIANO................................................................................................................................................................................... IT-34
NL NEDERLANDS............................................................................................................................................................................ NL-42
TABLE OF CONTENTS
Important Safeguards.................................................................................................................. EN - 3
Introduction.......................................................................................................................... EN - 3
Why Your Physician Prescribed Supplemental Oxygen ................................................................................... EN - 3
How Your Concentrator Works ...................................................................................................... EN - 3
Important Parts of Your Concentrator...................................................................................................... EN - 3
Setting Up Your Concentrator ........................................................................................................... EN - 4
Before Operating Your Concentrator ...................................................................................................... EN - 4
Operating Your Concentrator ............................................................................................................ EN - 4
DeVilbiss OSD®Operation.......................................................................................................... EN - 5
Reserve Oxygen System ............................................................................................................... EN - 5
Caring for Your Concentrator ............................................................................................................ EN - 5
Provider’s Notes...................................................................................................................... EN - 6
Troubleshooting ...................................................................................................................... EN - 6
Specifications ........................................................................................................................ EN - 7
Guidance and Manufacturer’s Declaration.................................................................................................. EN - 9
CAUTION– Federal (U.S.A.) law restricts this device to sale by or on the order of a physician.
INDICATIONS FOR USE– The DeVilbiss Oxygen Concentrator is intended for use as an oxygen concentrator to provide supplemental low ow oxygen therapy in the home,
nursing homes, patient care facilities, etc.
WARNING
Under certain circumstances, oxygen therapy can be hazardous. Seek medical advice before using an oxygen concentrator.
Physician Information
Physician Name:__________________________________________________________________
Telephone: ______________________________________________________________________
Address: _______________________________________________________________________
Prescription Information
Name: _________________________________________________________________________
Oxygen liters per minute
at rest:____________________ during activity:____________________ other: _____________
Oxygen use per day
Hours:_____________________________________ Minutes: ___________________________
Comments: ______________________________________________________________________
DeVilbiss Oxygen Concentrators (check one)
☐ 4-liter w/OSD, ☐5-liter, ☐5-liter w/OSD, Serial Number: ____________________________
DeVilbiss Equipment Provider Information
Set-Up Person: ___________________________________________________________________
This instruction guide was reviewed with me and I have been instructed on the safe use and care of
the DeVilbiss Oxygen Concentrator.
Signature:____________________________________________________ Date: ________________
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EN - 3
IMPORTANT SAFEGUARDS
Read this entire guide before using your DeVilbiss concentrator. Important information is highlighted by these terms throughout this guide:
DANGER Urgent safety information for hazards that will cause serious injury or death.
WARNING Important safety information for hazards that might cause serious injury.
CAUTION Information for preventing damage to the product.
NOTE Information to which you should pay special attention.
Important safeguards are indicated throughout this guide; pay special attention to all safety information.
READ ALL INSTRUCTIONS BEFORE USING.
SAVE THESE INSTRUCTIONS.
INTRODUCTION
This instruction guide will acquaint you with the DeVilbiss oxygen concentrator. Make sure that you read and understand this guide before operating your unit. Important
safeguards are indicated throughout this guide; pay special attention to all safety information. Contact your DeVilbiss equipment provider should you have any questions.
WARNING
For your safety, the oxygen concentrator must be used according to the prescription determined by your physician.
Equipment not suitable for use in the presence of a ammable anesthetic mixture with air or with oxygen or nitrous oxide.
This device contains electrical and/or electronic equipment. Follow local governing ordinances and recycling plans regarding disposal of device components.
DANGER
Oxygen causes rapid burning. Do not smoke while your oxygen concentrator is operating, or when you are near a person utilizing oxygen therapy. Do not use
within 5 feet (1.6m) of hot, sparking objects or naked sources of ame.
Why Your Physician Prescribed Supplemental Oxygen
Today, many people suffer from heart, lung, and other respiratory diseases. Many of these people can benet from supplemental oxygen therapy. Your body requires a steady
supply of oxygen to function properly. Your physician prescribed supplemental oxygen for you because you are not getting enough oxygen from room air alone. Supplemental
oxygen will increase the amount of oxygen that your body receives.
Supplemental oxygen is not addictive. Your physician prescribed a specic oxygen ow to improve symptoms such as headaches, drowsiness, confusion, fatigue, or increased
irritability. If these symptoms persist after you begin your supplemental oxygen program, consult your physician.
How Your DeVilbiss Oxygen Concentrator Works
Oxygen concentrators are the most reliable, efcient, and convenient source of supplemental oxygen available today. The oxygen concentrator is electrically operated. The unit
separates oxygen from room air which allows high-purity supplemental oxygen to be delivered to you through the oxygen outlet. Although the concentrator lters the oxygen in
a room, it will not affect the normal amount of oxygen in your room.
IMPORTANT PARTS OF YOUR CONCENTRATOR
Please take time to familiarize yourself with your DeVilbiss oxygen concentrator before operating.
Front View (Figure A)
1. Operating instructions
2. Green Power light – illuminates when your concentrator is operating
3. Power Switch
| = ON
O = OFF
4. Flow meter knob
5. Flow meter
6. Circuit breaker – resets the unit after electrical overload
shutdown
7. Oxygen outlet – oxygen is dispersed through this port
8. Normal Oxygen (green) light only on units w/OSD (see page 4)
9. Low Oxygen (yellow) light only on units w/OSD (see page 4)
10. Red Service Required light – when illuminated contact your DeVilbiss
provider
11. Line cord strap
Back View (Figure B)
12. Important Safeguards
13. Handgrip
14. Exhaust
15. Power cord and/or IEC power connector.
16. Air lter – prevents dirt, dust, and lint from entering your unit.
13
14
15
14
13
12
16
B
123
4
5
6
7
8
910
A
11
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DANGER
NO SMOKING

EN - 4
SETTING UP YOUR OXYGEN CONCENTRATOR
1. Position your unit near an electrical outlet in the room where you spend most of your time.
DANGER
Keep the oxygen concentrator at least 5 feet (1.6 m) from hot, sparking objects or naked sources of ame.
NOTE– Do not connect to an electrical outlet controlled by a wall switch. No other appliances should be plugged into the wall outlet.
2. Position your unit at least 6 inches (16 cm) from walls, draperies, or any other objects that might prevent the proper ow of air in and
out of your oxygen concentrator. The oxygen concentrator should be located so as to avoid pollutants or fumes.
BEFORE OPERATING YOUR OXYGEN CONCENTRATOR
1. Before operating your unit, always check to be sure the air lter (located on the back of your unit) is clean. Proper cleaning of this
lter is discussed in the Caring For Your Concentrator section on page 5.
2. Attach the appropriate oxygen accessories to the oxygen outlet.
Oxygen Tubing Connection:
a. Thread the oxygen outlet connector onto the oxygen outlet.
b. Attach the oxygen tubing directly to the connector (Figure 1).
Oxygen Tubing Connection With Humidication:
If your physician has prescribed an oxygen humidier as part of your therapy, follow these steps (If using a prell, go to step b.):
a. Fill the humidier bottle with distilled water. Do not overll.
b. Thread the wing nut located on the top of the humidier bottle to the oxygen outlet so that it is suspended (Figure 2). Make sure
it is securely tightened.
c. Attach the oxygen tubing directly to the humidier bottle outlet tting (Figure 3).
3. Your physician has prescribed either a nasal cannula or face mask. In most cases, they are already attached to the oxygen tubing. If
not, follow the manufacturer’s instructions for attachment.
4. Remove the power cord completely from the line cord strap. Make sure the power switch is in the “Off” position, and insert the plug
into the wall outlet. The unit is double insulated to guard against electric shock.
NOTE– (only 115 volt units) The plug on the DeVilbiss oxygen concentrator has one blade wider than the other. To reduce the risk of
electric shock, this plug is intended to t in a wall outlet only one way. Do not attempt to defeat this safety feature.
WARNING
Improper use of the power cord and plugs can cause a burn, re, or other electric shock hazards. Do not use the unit if the
power cord is damaged.
Only DeVilbiss Oxygen Concentrators with OSD
The OSD (Oxygen Sensing Device) is a device within your concentrator that monitors the oxygen produced by your unit. When the unit is turned “On,” all four lights (Power,
Service Required, Low Oxygen, and Normal Oxygen) on the front panel will illuminate briey. After a few seconds, only the Power and Normal Oxygen lights will remain lit.
The OSD lights on the front panel are dened as follows:
• Green Normal Oxygen light–acceptable oxygen level.
• Yellow Low Oxygen light– below an acceptable oxygen level.
If the oxygen purity falls below the acceptable level, the green Normal Oxygen light will shut off and the yellow Low Oxygen light will illuminate. Switch to your reserve
oxygen system. Refer to the Minor Troubleshooting section in this guide on page 6 and contact your DeVilbiss provider.
As an added safety feature should the oxygen purity continue to drop, an intermittent audible signal will sound. Contact your DeVilbiss provider immediately. Do not attempt
any other maintenance.
Accessories
Oxygen Outlet Connector - Plastic - 1/pack...................................................................................................................................................................................................... CN100
Bubble Humidifier........................................................................................................................................................................................................ Salter Labs 7600 or equivalent
There are many types of humidiers, oxygen tubing and cannulas/masks that can be used with this device. Certain humidiers and accessories may impair the device’s
performance. A mask or any nasal cannula can be used with continuous ow delivery and may be sized according to your prescription as recommended by your homecare
provider who should also give you advice on the proper usage, maintenance, and cleaning.
NOTE– A maximum of 50 feet (15 meters) of crush-proof oxygen tubing plus 7 feet (2.1 meters) of cannula plus a bubble humidier is allowed between the concentrator and
the patient.
NOTE– The oxygen supply accessory (patient tubing) shall be equipped with a means that in case of re stops the delivery of oxygen to the patient. This means of protection
should be located as close to the patient as practicable.
1
3
2
OPERATING YOUR DEVILBISS OXYGEN CONCENTRATOR
DANGER
Oxygen causes rapid burning. Do not smoke while your oxygen concentrator is operating, or when you are near a person
utilizing oxygen therapy. Keep the oxygen concentrator at least 5 feet (1.6 m) from hot, sparking objects or naked sources
of ame.
DANGER
Do not lay the cannula down while the concentrator is delivering oxygen. High concentrations of oxygen can cause rapid
burning.
1. Press the power switch to the “On” position. When the unit is turned on, the Power light will illuminate, and the patient alert
system – Service Required light and audible signal – will briey alarm.
SE-515X
DANGER
NO SMOKING

EN - 5
4
5
NOTE– If the Service Required light illuminates and the audible signal alarms but the unit is not operating, there is no power to the unit. Refer to the Minor Troubleshooting
chart on page 6 and contact your DeVilbiss provider if necessary.
NOTE– If an audible low-frequency vibration sound is detected, the unit is not operating properly. Refer to the Minor Troubleshooting chart on page 6, and contact your
DeVilbiss provider if necessary.
2. Check the ow meter to make sure that the ow meter ball is centered on the line next to the prescribed number of your ow rate.
CAUTION– It is very important to follow your oxygen prescription. Do not increase or decrease the ow of oxygen – consult your physician.
NOTE– Your DeVilbiss provider may have preset the ow meter so that it can not be adjusted.
NOTE– If the ow meter knob is turned clockwise, the ow decreases (and eventually will shut off the oxygen ow). If the knob is turned counterclockwise, the ow increases.
NOTE– For prescriptions of 5 LPM, be sure the ball is centered on the 5 liter line; the ball should not touch the red line. Setting the ow
higher than 5 may cause the oxygen purity level to drop.
NOTE– The low-ow alarm will activate if the ow meter ball is set below .3 lpm. The unit will continue to run; however, the Service
Required light will come on accompanied by an audible alarm. Adjust the ow meter to your prescribed ow.
NOTE–On later models of the 515 concentrators equipped with an OSD, the low-ow alarm may be activated if the ow meter ball is set
below 1 lpm. The unit will continue to run; however, the Service Required light will come on accompanied by an audible alarm. Adjust the
ow meter to your prescribed ow.
3. Your DeVilbiss concentrator is now ready for use, properly position the cannula or mask (Figure 4). Allow 20 minutes for oxygen
concentrator to reach stated performance.
RESERVE OXYGEN SYSTEM
As a precaution, your DeVilbiss provider may supply you with a reserve oxygen system. If your unit loses electrical power or fails to operate correctly, the Patient Alert System
will sound to signal you to switch to your reserve oxygen system (if provided) and contact your DeVilbiss provider.
CARING FOR YOUR DEVILBISS OXYGEN CONCENTRATOR
NOTE–Use no lubricants, oils or grease.
WARNING
Before attempting any cleaning procedures, turn the unit “Off.”
Cannula/Mask, Tubing, and Humidifier Bottle
Clean and replace the cannula/mask, tubing, and humidier bottle according to the manufacturer’s instructions.
Air Filter and Oxygen Outlet Connector
The air lter and connector should be cleaned at least once a week. To clean, follow these steps:
1. Remove the air lter, located on the back of the unit. Remove the oxygen outlet connector (if used).
2. Wash in a solution of warm water and dishwashing detergent (Figure 5).
3. Rinse thoroughly with warm tap water and towel dry. The lter should be completely dry before reinstalling.
CAUTION– To prevent product damage, do not attempt to operate the unit without the air lter or while the lter is still damp.
Exterior Cabinet
As needed, clean the concentrator exterior cabinet by using a damp cloth or sponge with a mild household cleaner and wipe it dry.
WARNING
To avoid electric shock, do not remove the concentrator cabinet. The cabinet should only be removed by a qualied DeVilbiss technician. Do not apply liquid
directly to the cabinet or utilize any petroleum-based solvents or cleaning agents.
Use of harsh chemicals (including alcohol) is not recommended. If bactericidal cleaning is required, a non-alcohol based product should be used to avoid
inadvertent damage.
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), and
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 qualied DeVilbiss
provider/service technician.
NOTE–If the following described complete processing of the concentrator by a qualied 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 qualied 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 humidier
bottle.
2. CAUTION–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 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 lter on the back of the device.
7. Check the oxygen concentration. If the device is within specications, the extended life intake bacteria lter does not need to be replaced between patients. If the
concentration is not within specications, the provider should refer to the service manual section on Troubleshooting.
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EN - 6
TROUBLESHOOTING
The following troubleshooting chart will help you analyze and correct minor oxygen concentrator malfunctions. If the suggested procedures do not help, switch to your reserve
oxygen system and call your DeVilbiss homecare provider. Do not attempt any other maintenance.
WARNING
To avoid electric shock hazard, do not remove the cabinet. The cabinet should only be removed by a qualied DeVilbiss homecare technician.
Minor Troubleshooting Chart
SYMPTOM POSSIBLE CAUSE REMEDY
A. Unit does not operate. Power light is off when the
power switch is “On.” Audible alert is pulsing and
Service Required light is ashing.
1. Power cord not properly inserted
into wall outlet. 1. Check power cord connection at the wall outlet. On 230 volt units, also check the mains connection on the back of the unit.
2. No power at wall outlet. 2. Check your home circuit breaker and reset if necessary. Use a different
wall outlet if the situation occurs again.
3. Oxygen concentrator circuit
breaker activated. 3. Press the concentrator circuit breaker reset button located below the power switch. Use a different wall outlet if the situation occurs again.
If the above remedies do not work, contact your DeVilbiss provider.
B. Unit operates, the Power light is on when the
power switch is “On.” Red Service Required light
is illuminated. Audible alert may be sounding.
1. Air lter is blocked. 1. Check the air lter. If the lter is dirty, wash it following the cleaning
instructions on page 5.
2. Exhaust is blocked. 2. Check the exhaust area; make sure there is nothing restricting the unit
exhaust.
3. Blocked or defective cannula, face
mask, or oxygen tubing.
3. Detach cannula or face mask. If proper ow is restored, clean or replace
if necessary. Disconnect the oxygen tubing at the oxygen outlet. If
proper ow is restored, check oxygen tubing for obstructions or kinks.
Replace if necessary.
4. Blocked or defective humidier
bottle. 4. Detach the humidier from the oxygen outlet. If proper ow is obtained, clean or replace humidier.
5. Flow meter set too low. 5. Set ow meter to prescribed ow rate.
If the above remedies do not work, contact your DeVilbiss provider.
C. Unit operates, the power light is on when power
switch is “on,” audible low-frequency vibration
sound is detected.
1. Turn your unit “Off.” Switch to your reserve oxygen system, and contact
your DeVilbiss provider immediately.
D. If any other problems occur with your oxygen
concentrator. 1. Turn your unit “Off.” Switch to your reserve oxygen system, and contact your DeVilbiss provider immediately.
Minor Troubleshooting Chart - only OSD Concentrators
A. Both the green Normal Oxygen and the yellow
Low Oxygen lights are either on or off. 1. OSD malfunction. 1. Contact your DeVilbiss provider.
B. Yellow Low Oxygen light is on or the yellow Low
Oxygen light is on and the intermittent audible
signal is sounding.
1. Flow meter is not properly set. 1. Ensure the ow meter is properly set to the prescribed number.
2. Air lter is blocked. 2. Check the air lter. If the lter is dirty, wash it following the cleaning
instructions on page 5.
3. Exhaust is blocked. 3. Check the exhaust area; make sure there is nothing restricting the unit
exhaust.
If the above remedies do not work, contact your DeVilbiss provider.
C. Red Service Required light is on and an
intermittent audible signal is sounding. 1. Flow meter is not properly set. 1. Ensure the ow meter is properly set to the prescribed number.
2. Air lter is blocked. 2. Check the air lter. If the lter is dirty, wash it following the cleaning
instructions on page 5.
3. Exhaust is blocked. 3. Check the exhaust area; make sure there is nothing restricting the unit
exhaust.
If the above remedies do not work, contact your DeVilbiss provider.
SE-515X

EN - 7
SPECIFICATIONS
DEVILBISS 4-LITER AND 5-LITER SERIES
Catalog Number 515ADS/515ADZ
515DS/515DZ
515AKS/515AKZ
515KS/515KZ/515NS 515UK 4-Liter
Delivery Rate (Lower delivery rates
available for low ow applications) 1 to 5 LPM 1 to 5 LPM 1 to 4 LPM
Maximum Recommended Flow (@
nominal outlet pressures of zero and 7
kPa) 5 LPM 5 LPM 4 LPM
Outlet Pressure 8.5 psig (58.6 kPa) 8.5 psig (58.6 kPa) 8.5 psig (58.6 kPa)
Electrical Rating
515A Series - 115 V, 60 Hz, 4.1 Amp 515A Series -220-230 V~, 50 Hz, 1.7 Amp
230 V~, 60 Hz, 2.4 Amp 230 V~, 50 Hz, 1.4 Amp
515 Series - 115 V, 60 Hz, 4.2 Amp 515 Series - 220-230 V~, 50 Hz, 1.7 Amp
230 V~, 60 Hz, 1.9 Amp
Operating Voltage Range 97-127 V~, 60 Hz 187-255 V~, 50 Hz
218-253 V~, 60 Hz 195-253 V~, 50 Hz
Oxygen Percentage 1-5 LPM=93%±3% 1-5 LPM=93%±3% 1-4 LPM=93%±3%
Operating Altitude
(tested at 21°C only)
0-1500 M (0-4921 ft) Across the voltage range: No degradation of performance Across the voltage range: No degradation of performance Across the voltage range: No degradation of performance
1500-3000 M (4921-9842 ft)
515A Series
Tested at nominal voltage only:
No degradation in performance expected
based on tests of similar products.
515A Series
Tested at 230V/50Hz only:
No degradation in performance expected
based on tests of similar products. Not recommended/Not tested
515 Series
Tested at nominal voltage only:
No degradation in performance
515 Series
Tested at 230V/50Hz only:
~4% oxygen performance drop at 5 LPM
3000-4000 M (9842-13123 ft) Not recommended/Not tested Not recommended/Not tested Not recommended/Not tested
Operating Environment Range*
10°C to 35°C, humidity range of 30%
to 75%
515A Series - No degradation in
performance up to 40°C across the
operating voltage range. (tested at 670 m).
515A Series - No degradation in
performance up to 40°C across the
operating voltage range. (tested at 670 m). No degradation in performance across
the operating voltage range (tested @
sea level).
515 Series - No degradation in performance
across the operating voltage range (tested
@ sea level)
515 Series - ~4% oxygen performance drop
at 5 LPM and 35˚C condition. No
degradation in performance across the
operating voltage range at other liter ows
(tested at 670 M).
Power Consumption
515A Series - 385 Watts Average
515ADS Only - 320 Watts @ 2.5 LPM &
below
515 Series - 400 Watts Average
515A Series - 230V / 50 Hz - 330 Watts
Average
230V / 50 Hz - 305 Watts Average 515AKS
Only @ 2.5 LPM & below
515 Series - 230V / 50 Hz – 365 Watts
Average
515A Series - 230V / 60 Hz - 450 Watts
Average
230V / 60 Hz 515AKS Only - 415 Watts
Average @ 2.5 LPM & below
515 Series – 230V / 60Hz – 435 Watts
Average
295 Watts Average
Weight 515A Series - 50 lbs. (22.7 Kilograms) 515A Series - 50 lbs. (22.7 Kilograms) 53 lbs. (24.5 Kilograms)
515 Series - 52 lbs. (23.5 Kilograms) 515 Series - 53 lbs. (24.5 Kilograms)
Sound Level (ISO 8359:1996 from
front)
515A Series - 48 dbA overall average 515A Series - 48 dbA (50Hz) overall
average 50.5 dbA overall average
515 Series - 52.5 dbA overall average** 515 Series - 50.5 dbA (50Hz) overall
average
Dimensions 27.75”H x 16”W x 14”D
(70.5 x 40.6 x 35.6 cm) 27.75”H x 16”W x 14”D (70.5 x 40.6 x 35.6 cm) 27.75”H x 16”W x 14”D (70.5 x 40.6 x 35.6 cm)
Pressure Relief Valve
515A Series - 40 psig±5psig
(276 kPa±34.5 kPa) 515A Series - 40 psig±5psig (276 kPa±34.5 kPa) 44 psig±3psig (303 kPa±2.1 kPa)
515 Series - 44 psig±3psig
(303 kPa±21 kPa) 515 Series - 44 psig±3psig (303 kPa±21 kPa)
SE-515X

EN - 8
DEVILBISS 4-LITER AND 5-LITER SERIES
Catalog Number 515ADS/515ADZ
515DS/515DZ
515AKS/515AKZ
515KS/515KZ/515NS 515UK 4-Liter
Operating System Time Cycle / Pressure Swing Time Cycle / Pressure Swing Time Cycle / Pressure Swing
For units equipped with an OSD, the
visible “low oxygen” indicator will
activate at the following level
515A Series
84% ± 2%
(The audible alarm will alert at
approximately 75%. At less than 60%, the
red “service required” light will activate.)
515A Series
84% ± 2%
(The audible alarm will alert at
approximately 75%. At less than 60%, the
red “service required” light will activate.)
Units with serial numbers less than
H20000: 85%± 2% (The audible alarm
will alert at approximately 75%).
Units with serial numbers of H20000
and greater: 83.5%± 1.5%. (The
audible alarm will alert at
approximately 75%. At less than 60%,
the red “service required” light will
activate.)
515 Series
Units with serial numbers less than H20000:
85%± 2% (The audible alarm will alert at
approximately 75%).
Units with serial numbers of H20000 and
greater: 83.5%± 1.5%. (The audible alarm
will alert at approximately 75%. At less than
60%, the red “service required” light will
activate.)
515 Series
Units with serial numbers less than H20000:
85%± 2% (The audible alarm will alert at
approximately 75%).
Units with serial numbers of H20000 and
greater: 83.5%± 1.5%. (The audible alarm
will alert at approximately 75%. At less than
60%, the red “service required” light will
activate.)
Storage Conditions -40°C to 70°C, humidity range of 10% to
100%, including condensation
-40°C to 70°C, humidity range of 10% to
100%, including condensation
-40°C to 70°C, humidity range of 10%
to 100%, including condensation
Equipment Class and Type
Class II Equipment Double Insulated;
Type B Applied Part
Ordinary Equipment, IPX0
Class II Equipment Double Insulated;
Type B Applied Part
Ordinary Equipment, IPX0
Class II Equipment Double
Insulated;
Type B Applied Part
Ordinary Equipment, IPX0
Approval Body and Safety Standard CSA
CAN/CSA-C22.2 No. 601.1-M90
515A Series
TUV
IEC 60601-1
EN 60601+A1+A2
ISO8359:1996 (515AKZ excluded) TUV
IEC 601-1+A1+A2
EN 60601+A1+A2
ISO8359:1996
515 Series
TUV
IEC 601-1+A1+A2
EN 60601+A1+A2
ISO8359:1996 (515KZ excluded)
EMC Compliance To 515A Series - IEC 60601-1-2 515A Series - IEC 60601-1-2 IEC 601-1-2
515 Series - IEC 601-1-2 515 Series - IEC 601-1-2
*NOTE: The OSD performance at 10°C to 35°C, 95% R.H. through voltage range on the 515ADS/515AKS/515DS veried at 670m.
**NOTE: This corresponds with a sound level of 50 dbA overall average as measured according to the guidelines of the now defunct ANSI Z79.123-1981 standard.
Specications subject to change without notice.
SE-515X

EN - 9
DEVILBISS GUIDANCE AND MANUFACTURER’S DECLARATION
WARNING
Medical Electrical Equipment needs special precautions regarding EMC and needs to be installed and put into service according to the Electromagnetic
Compatibility [EMC] information provided in the accompanying documents.
Portable and Mobile RF Communications Equipment can affect Medical Electrical Equipment.
The equipment or system should not be used adjacent to or stacked with other equipment and that if adjacent or stacked use is necessary, the equipment or
system should be observed to verify normal operation in the conguration in which it will be used.
NOTE– The EMC tables and other guidelines provide information to the customer or user that is essential in determining the suitability of the Equipment or System for the
Electromagnetic Environment of use, and in managing the Electromagnetic Environment of use to permit the Equipment or System to perform its intended use without
disturbing other Equipment and Systems or non-medical electrical equipment.
Guidance and Manufacturer’s Declaration – Electromagnetic Emissions
This device is intended for use in the electromagnetic environment specied below. The customer or the user of this device should assure that it is used in such an
environment.
Emissions Test Compliance Electromagnetic Environment – Guidance
RF Emissions CISPR 11 Group 1 This device uses RF energy only for its internal function. Therefore, its RF emissions are very low and
are not likely to cause any interference in nearby electronic equipment.
RF Emissions CISPR 11 Class B This device is suitable for use in all establishments including domestic and those directly connected to
the public low-voltage power supply network that supplies buildings used for domestic purposes.
Harmonic emissions IEC 61000-3-2 Class B
Voltage uctuations / icker emissions Complies
Guidance and Manufacturer’s Declaration – Electromagnetic Immunity
This device is intended for use in the electromagnetic environment specied below. The customer or the user of this device should assure that it is used in such an
environment.
Immunity Test
IEC 60601 Test
Level
Compliance
Level Electromagnetic Environment - Guidance
Electrostatic discharge (ESD)
IEC 61000-4-2
±6kV contact
±8kV air Complies Floors should be wood, concrete, or ceramic tile. If oors are covered with
synthetic material, the relative humidity should be at least 30%
Radiated RF IEC 61000-4-3 3 V/m 80MHz to 2.5GHz Complies Field strengths outside the shielded location from xed RF transmitters, as
determined by an electromagnetic site survey, should be less than 3 V/m.
Interference may occur in the vicinity of equipment marked with the following
symbol:
Conducted RF IEC 61000-4-6 3 Vrms 150kHz to 80MHz Complies
Electrical fast transient
IEC 61000-4-4
±2kV power line
±1kV I/O lines Complies Mains power quality should be that of a typical commercial or hospital
environment.
Surge IEC 61000-4-5 ±1kV differential
±2kV common Complies
Power frequency magnetic eld
IEC 61000-4-8 3 A/m Complies Power frequency magnetic elds should be at levels characteristic of a typical
location in a typical commercial or hospital environment.
Voltage dips, short interrupts and
voltage variations on power supply
input lines IEC 61000-4-11
>95% dip 0.5 cycle
60% dip 5 cycles
70% dip 25 cycles
95% dip 5 secs.
Complies
Mains power quality should be that of a typical commercial or hospital
environment. If the user of this device requires continued operation during power
mains interruptions, it is recommended that the device be powered from an
uninterruptible power supply or battery.
SE-515X