Datasheet

DocID:LAB-6888194 version:01 status: Approved

Servo-n
2018-06-29 10:02 by Jennie Haag u2411101

System version 3.0

This document is intended to provide information to an international audience outside of the US.
 Contents

Technical specifications................................................................. 3
General................................................................................................... 3
The ventilator – general................................................................... 3
Ventilation – general......................................................................... 4
User interface...................................................................................... 4
Power supply........................................................................................ 4
Gas supply............................................................................................. 4
Operating conditions........................................................................ 5
Non operating conditions............................................................... 5
Standards – safety and functionality......................................... 5
Display.................................................................................................... 5
Ventilation modes – invasive ventilation................................... 6
Invasive ventilation........................................................................... 6
Ventilation modes – non invasive ventilation.......................... 6
Non invasive ventilation.................................................................. 6
High flow therapy (option).............................................................. 6
Open Lung Tool trends (option).................................................... 7
High Frequency Oscillatory Ventilation (option).................... 7
Parameter settings............................................................................ 7
Backup parameter settings............................................................ 8
Special functions................................................................................ 8
Disconnection / Suction.................................................................. 8
Monitoring and trends...................................................................... 8
Alarms..................................................................................................... 9
Autoset (alarm limits) specification............................................ 9
Y sensor (option)................................................................................. 10
CO2 analyzer (option) ...................................................................... 10
Edi module (option)........................................................................... 11
Aerogen nebulizers............................................................................ 11
Communication / Interface............................................................ 11
Log function......................................................................................... 11
Saving of data...................................................................................... 12
Optional equipment.......................................................................... 12
Compressor Mini (option)............................................................... 12
Service.................................................................................................... 12
DocID:LAB-6888194 version:01 status: Approved

Ordering information...................................................................... 13
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Dimensional drawings.................................................................... 14
Servo-n on mobile cart..................................................................... 14
Servo-n holder..................................................................................... 14
Servo-n (patient unit) on Servo-n holder.................................. 14

2 GETINGE • SERVO -N
 Servo-n
Technical specifications

General The ventilator – general

Intended use The Servo-n ventilator system is: Servo-n Servo-n on

mobile cart
• intended for respiratory support,
monitoring and treatment of neona- Base system weight Approximately Approximately
tal and pediatric patients 23 kg (50.7 lbs) 35 kg (77.2 lbs)
• to be used only by healthcare pro- • Patient unit • Base system
viders 15 kg (33.0 lbs) approx. 23 kg
• to be used only in professional • User interface (50.7 lbs)
healthcare facilities and for trans- 4 kg (8.8 lbs) • Mobile cart
port within these facilities • Handle 3 kg 13.0 kg (28.7 lbs)
(6.6 lbs)
For NAVA and Edi monitoring, it is in • Cable holder
addition intended: and cable 1 kg
• to provide monitoring of the (2.2 lbs)
patient’s breathing drive
Dimensions of base 368 x 205 mm 647 x 547 mm
• to improve synchrony between the
(W x D), see dimen- (14.5" x 8.1") (25.5" x 21.5")
ventilator system and patient when
sional drawings incl. wheels
the electrical signal from the brain
Height (incl. user 826 mm (32.5") 1368 mm (53.8")
to the diaphragm is active
interface)
• for use on all patients with no
contraindication for insertion/ Wheels N/A Four wheels with
exchange of a nasogastric tubes separate brakes

Instructions for use Please carefully read the user’s A-weighted sound <40 dB, measured at a distance of 1 m
manual pressure level (LpA) (3.3 ft)

Legal manufacturer Maquet Critical Care AB A-weighted sound <51 dB

power level (LWA)
Other products See separate data sheets.

Contact your local Getinge supplier

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for more information.

2018-06-29 10:02 by Jennie Haag u2411101

GETINGE • SERVO -N 3
 Ventilation – general Power supply

Patient range • Neonatal: 0.3–8 kg (0.7–17.6 lbs) Power supply, auto- • 100–120 V AC, 2 A, 50–60 Hz
• Pediatric: 3–30 kg (6.6–66.0 lbs) matic range selection • 220–240 V AC, 1 A, 50–60 Hz

Bias flow 0.5 l/min * Plug-in battery module:

• Battery backup • Six battery module slots. Two bat-
Internal compress- Max. 0.1 ml/cmH2O
(­nickel-metal hydride, teries are delivered with the venti-
ible factor
NiMH) lator.
Gas delivery system Microprocessor controlled valves
• Battery capacity • Rechargeable, 12 V, 3.5 Ah each
Maximum airway 125 cmH2O • Battery backup time • Ranging from 60 minutes (2 batteries)
pressure to 180 minutes (6 batteries)
• Recharge time • Approximately 3 h/battery
Method of trigger- Flow, pressure and Edi (with Edi module
ing and Edi catheter) External 12 V DC 12.0 V–15.0 V DC, 10 A

Inspiratory flow 0 to 33 l/min * Typical min. power con- 100 VA, 40 W at 230 V or 75 VA, 40 W
range sumption (no optional at 110 V
modules, no ongoing
Pressure drop • Max. 6 cmH2O at a flow of 60 l/min
battery charging,
(insp. channel)
normal panel back-
• Max. 3 cmH2O at a flow of 60 l/min
light)
(exp. channel)
Typical max. power 200 VA, 80 W at 230 V or 170 VA, 80 W
PEEP regulation Microprocessor controlled valve
consumption (with at 110 V
Rise time, expiratory <12 ms for 10–90 % response at flow of
CO2), Edi and Y sensor
flow measurement 3–192 l/min
modules, ongoing bat-
Expiratory flow 0 to 192 l/min tery charging, max.
range panel backlight)

* In HFOV, adaptive BIAS flow and extended flow range.

Gas supply
User interface
Inlet gas pressure 200–600 kPa / 2.0–6.0 bar / 29–87 PSI
air/O2 (HFOV performance may be limited at
Type TFT-LCD touchscreen
low inlet gas pressures. See users
Size 366 x 300 x 50 mm (14.4" x 11.8" x 2.0")
instruction for details.)
Viewing area 15" XGA, 1024 x 768 pixels with a
Connection stan- AGA, DISS, NIST, or French standard
24-bit color palette
dards available
Weight Approximately 4 kg (8.8 lbs)
Unavailable gas/loss The flow from an unavailable gas (air or
of gas pressure O2) is automatically compensated for
so that the patient gets the preset
volume and pressure.
DocID:LAB-6888194 version:01 status: Approved

Patient system gas Male 22 mm / female 15 mm. In accor-

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connectors dance with ISO 5356-1

Gas exhaust port Male 30 mm cone

4 GETINGE • SERVO -N
 Operating conditions
Operating temperature
Relative humidity
Atmospheric pressure
Lowest pressure in
patient circuit
Display
Views • Basic view
+10 to +40ºC (+50 to +104ºF)
• Advanced view
15 to 95% non-condensing
• Loops view
660 to 1060 hPa • Distance view
(HFOV performance may be limited • Family view
at high altitudes. See users • Servo Compass (option)
instruction for details.) Each of the screen layout views offers a
specific combination of displayed wave-
-400 cmH2O
forms, loops and presented values.
Real time wave- • Pressure
forms • Flow
• Volume
• CO2 (with CO2 analyzer option)

Non operating conditions • Edi (with Edi module and Edi catheter)

Loops • Pressure – Volume

Temperature
Relative humidity
Atmospheric pressure
• Pressure – Flow
-25 to +60ºC (-13 to +140ºF)
• Volume – Flow
<95% condensing
A reference loop and three overlaying
470 to 1060 hPa loops can be displayed.

Lowest pressure in patient N/A Servo Compass Visualizes volume (VT/BW) and pressure
circuit (total or driving) in relation to set targets
in invasive modes.

Monitoring Possibility to combine waveforms with trends of

trends displayed monitored values in one view
(15 min –72 h).
Standards – safety and functionality

The device complies with requirements

0123
and classification IIb of Medical Device
Directive 93/42/EEC.

CE Mark Notified Body number: 0123.

Classification IEC 60601-1: 2005, Class I, continuous

operation.

Standards • ISO 80601-2-12:2011,

ISO 80601-2-55:2011,
EN 13544-1:2007+A1:2009
• IEC 60601-1, Type B (equipment making
physical contact with the patient and
the gas pathways).
• IEC 60601-1, Type BF (CO2 analyzer, Y
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sensor, nebulizer patient unit and

2018-06-29 10:02 by Jennie Haag u2411101

cable)
• IEC 60601-1, Type CF defibrillation
proof (Edi catheter and cable)

Ingress protection IP 21

Electromagnetic According to limits specified in IEC

compatibility (EMC) 60601-1-2:2014

The ‘EMC Declaration, Information to the Responsible

Organization’ is available from the manufacturer.

GETINGE • SERVO -N 5
 Ventilation modes – invasive Ventilation modes – non invasive
ventilation ventilation

Controlled ventilation • PC (Pressure Control) Controlled ventilation • NIV PC (option)

• VC (Volume Control)
Supported ventilation • NIV PS (option)
• PRVC (Pressure Regulated Volume
• Nasal CPAP
Control)
NIV NAVA • Neurally Adjusted Ventilatory Assist
• HFOV (Amplitude Control)
via non-invasive patient interfaces
• HFOV (V TGT) (Volume Target)
NIV PS is not available in the neonatal patient category
Supported ventilation: • PS/CPAP (Pressure Support / Con-
tinuous Positive Airway Pressure)
• VS (Volume Support)

Automode (option) • Control mode: VC <–>

Support mode: VS
• Control mode: PC <–> Non invasive ventilation
Support mode: PS
• Control mode: PRVC <–>
Max. leakage compen- • Pediatric and neonatal:
Support mode: VS
sation level -- Inspiratory: up to 33 l/min
Combined ventilation • SIMV (VC) + PS (Synchronized -- Expiratory: up to 25 l/min
Intermittent Mandatory Ventila- -- Nasal CPAP: up to 20 l/min
tion)
Disconnection flow • Low:
• SIMV (PC) + PS
(configurable) -- 7.5 l/min
• SIMV (PRVC) + PS
• High:
• Bi-Vent/APRV (Airway Pressure
-- 15 l/min
Release Ventilation) (option)
• Disabled: the ventilator system will
NAVA • Neurally Adjusted Ventilatory continue to deliver assist even
Assist via endotracheal tube or tra- when leakage is excessive.
cheostomy
Connection detection Manual or automatic via bias flow
VC and SIMV (VC) + PS and Automode VC <–> VS are not avail-
able in the neonatal patient category.

HFOV and HFOV (V TGT) are only available in neonatal patient

­category
High flow therapy (option)

Flow setting range • Pediatric:

-- 0.5–30 l/min

Invasive ventilation • Neonatal:

-- 0.5–20 l/min

Max. leakage compensation level • Neonatal:

-- 25 l/min
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6 GETINGE • SERVO -N
 Open Lung Tool trends (option) Parameter settings

Graphical trend areas 1. - EIP (end-inspiratory pressure) Parameter Neonatal Pediatric

range range
- Pdrive *
- PEEP Tidal volume (ml) 2–50 10–350
2. - VTCO2 (when applicable)
Minute volume (l/min) 0.1–7.5 0.3–20
- Cdyn
Apnea, time to alarm (s) 1–45 2–45
3. - VTi
- VTe Max. apnea time in Automode (s) 3–15 3–15

* Pdrive only shown as values – not graphical trends Pressure level above PEEP (cmH2O) 0–60 0–60

Modes All invasive modes Pressure level above PEEP (in NIV) 0–30 0–30
(cmH2O)
Trend time 5, 10, 15, 30, or 60 minutes
Pmean (HFOV) (cmH2O) 5–40 –

Pamp (HFOV) (cmH2O) 0–100 –

Tidal Volume (HFOV) (ml) 0.2–40 –

I:E ratio (HFOV) 1:2–1:1 –

Frequency (HFOV) (Hz) 5–20 –

PEEP (cmH2O) 1–50 1–50

PEEP in NIV (cmH2O) 2–20 2–20

CPAP pressure (cmH2O) 2–20 2–20

Respiratory rate (breaths/min) 4–150 4–150

SIMV rate (breaths/min) 1–60 1–60

Breath cycle time, SIMV (s) 0.5–15 0.5–15

PHigh (cmH2O) 2–50 2–50

THigh (s) 0.2–30 0.2–30

TPEEP (s) 0.1–10 0.1–10

PS above PHigh (cmH2O) 0–78 0–78

O2 concentration (%) 21–100 21–100

I:E ratio 1:10–4:1 1:10–4:1

Ti (s) 0.1–5 0.1–5

NAVA level (cmH2O/μV) 0–15 0–15

Edi trigger (μV) 0.1–2.0 0.1–2.0

TPause (s) – 0–1.5

TPause (% of breath cycle time) – 0–30

Flow trigger (l/min) 0–0.5 0–0.5

Pressure trigger (cmH2O) -1 to -20 -1 to -20

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Insp. rise time (% of breath cycle 0–20 0–20

time)

Insp. rise time (s) 0–0.2 0–0.2

End inspiration (% of peak flow) 1–70 1–70

End inspiration (% of peak flow) in 10–70 10–70

NIV

GETINGE • SERVO -N 7
 Backup parameter settings Monitoring and trends

Parameter Neonatal Pediatric Peak airway pressure Ppeak

range range
Pause airway pressure Pplat
Inspiratory tidal volume (ml) 2–50 10–350
Mean airway pressure Pmean
Pressure level above PEEP in backup 5–60 5–60
Driving pressure Pdrive
(cmH2O)
Positive end expiratory pressure PEEP
Pressure level above PEEP in NIV 5–30 5–30
Continuous positive airway pressure CPAP
backup (cmH2O)
Spontaneous breaths per minute RR sp
Respiratory rate in backup (breaths/ 4–150 4–150
Respiratory rate RR
min)
Spontaneous expiratory minute volume MVe sp
I:E ratio 1:10–4:1 1:10–4:1
Inspired minute volume MVi
Ti (s) 0.1–5 0.1–5
Expired minute volume MVe
Leakage fraction (%) Leakage

Inspired tidal volume VTi

Expired tidal volume VTe

Special functions End expiratory flow Flowee

Measured oxygen concentration O2 conc

Special function Setting range
CO2 end tidal concentration etCO2
Manual breath Initiation of 1 breath (In SIMV mode
CO2 minute elimination VCO2
initiation of 1 mandatory breath)
CO2 tidal elimination VTCO2
Static measurements Insp. or exp. hold (0–30 seconds)
CO2 Diffusion (HFOV) DCO2
Nebulization 5–30 min/Continuous/Off
Dynamic compliance Cdyn
O2 boost level Off, 1–78 %, 100%
Static compliance Cstatic
O2 boost function Activate O2 boost up to 1 minute
Inspiratory resistance Ri
Leakage compensation On/Off
Expiratory resistance Re
Circuit compensation On/Off
Work of breathing, ventilator WOBvent
Edi monitoring In all ventilation modes and in Work of breathing, patient WOBpat
Standby (with Edi module and Edi
Elastance E
catheter)
P 0.1 P 0.1
Previous mode Activates previously used mode
Shallow Breathing Index SBI
Backup ventilation Backup On/Off
Peak Edi value Edipeak
Apnea management Several parameters
Average Edipeak Edipeak average
Pause oscillation Pause oscillation during HFOV (monitoring only)
Average Edimin Edimin average
(monitoring only)
Minimum Edi value Edimin
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Ratio of expired tidal volume to body weight VT/BW

Disconnection / Suction Switches to backup per minute Backup ∑ (trended
value only)
Pre-oxygenation time Max. 2 min Time in backup in percent per minute Backup % (trended
value only)
Post-oxygenation time Max. 1 min
Tidal Volume (HFOV) VTHF
Patient disconnected High priority alarm activated after
Pressure Amplitude (HFOV) Pamp
1 min
I:E-ratio (HFOV) I:EHF
Adjustable oxygen level 21 – 100 %

8 GETINGE • SERVO -N
 Alarms Autoset (alarm limits) specification

Alarm Neonatal Pediatric Autoset (alarm limits) Invasive ventilation, controlled

range range specification modes only
Airway pressure (upper alarm limit) 16–90 16–90
High airway pressure Mean peak pressure +10 cmH2O
cmH2O cmH2O
or at least 35 cmH2O
Airway pressure NIV (upper alarm 16–70 16–70
Inspiratory tidal volume The greater of VTi + 30 % or
limit) cmH2O cmH2O
too high VTi +2 ml
Respiratory rate (upper alarm limit) 2–160 2–160
Expiratory minute volume Mean expiratory minute volume
breaths/ breaths/
(upper alarm limit) +50 %
min min
Expiratory minute volume Mean expiratory minute volume
Respiratory rate (lower alarm limit) 1–159 1–159
(lower alarm limit) -50 %
breaths/ breaths/
Respiratory rate (upper Mean respiratory rate +40 %
min min
alarm limit)
Expired minute volume (upper alarm 0.02–30 0.02–30
Respiratory rate (lower Mean respiratory rate -40 %
limit) l/min l/min
alarm limit)
Expired minute volume (lower alarm 0.01 – 20 0.01 – 20
End expiratory pressure Mean end expiratory pressure
limit) l/min l/min
(upper alarm limit) +5 cmH2O
End expiratory pressure (upper 1–55 1–55
End expiratory pressure Mean end expiratory pressure
alarm limit) cmH2O cmH2O
(lower alarm limit) -3 cmH2O
End expiratory pressure (lower Off, 1–47 Off, 1–47
End tidal CO2 concentra- Mean end tidal CO2 concentra-
alarm limit) cmH2O cmH2O
tion (upper alarm limit) tion +25 %
No patient effort (Apnea) alarm 1–45 s 2–45 s
End tidal CO2 concentra- Mean end tidal CO2 concentra-
Automatic return to support mode on patient triggering
tion (lower alarm limit) tion -25 %
No consistent patient effort Yes, described in User’s
High frequency Tidal High frequency Tidal Volume
manual
Volume in HFOV (upper +22 % *
High continuous pressure Yes, described in User’s alarm limit)
manual
High frequency Tidal High frequency Tidal Volume
O2 concentration Set value ±5 vol% or Volume in HFOV (lower -29 % *
≤18 vol% alarm limit)

Gas supply Below 200 kPa (2.0 Pressure amplitude in Mean Pressure amplitude in
bar/29 PSI), above 600 HFOV (V TGT) (upper alarm HFOV +40 % *
kPa (6.0 bar/87 PSI) limit)

Battery • Limited battery Pressure amplitude in Mean Pressure amplitude in

capacity: 10 min. HFOV (V TGT) (lower alarm HFOV -40 % *
• No battery capacity: limit)
less than 3 min
* These alarm limits correspond to a 50 % increase / decrease of DCO2
• Low battery voltage.

End tidal CO2 (upper and lower limit) 0.5–19.9 %,

4–99mmHg,
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0.5–13.9kPa
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Leakage too high Yes, described in User’s

manual

Technical Yes, described in User’s

manual

Mean Airway Pressure (HFOV) High / Yes –

Low

Pressure amplitude (HFOV) High / Low Yes –

VTHF High / Low Yes –

VTHF Limited Yes –

GETINGE • SERVO -N 9
 Y sensor (option) CO2 analyzer (option)

Y sensor Size Weight CO2 analyzer Size Weight

(option) (option)

Y sensor module W 154 x L 90 x H 21 mm 280 g (0.6 lbs) CO2 analyzer module W 154 x L 90 x H 21 mm 265 g
(W 6.1" x L 3.5" x H 0.8") (W 6.1" x L 3.5" x H 0.8") (0.58 lbs)

Y sensor W 18 x L 50 x H 27 mm 11 g Sensor (Capnostat 5) 32.0 x 47.0 x 21.6 mm 20 g

(W 0.7" x L 2.0" x H 1.1") (1.3" x 1.9" x 0.8")

Connectors and • 15 mm male and female conical connector Operating temperature 10 to 33 °C (50 to 91 °F)
cables on flow sensor according to ISO 5356-1
Airway adapter 10 g
• Pressure port on module, pressure line,
Power source Powered by the ventilator
2.0 m (6.6 ft), phthalate free PVC
• Flow sensor cable, 2.0 m (6.6 ft) Connectors and cables Sensor 2.8 m (9.2
ft) cable
Sensor material • Single use: PC, Polycarbonate
• Reusable: PEI, Polyetherimide or PSF, Poly- Measuring method Mainstream, dual-wavelength,
sulfone non-dispersive infrared

Power source Powered by the ventilator system, ≤4.5 W Parameters • CO2 end tidal concentration
during normal operation (etCO2)
• CO2 minute elimination (VCO2)
Measuring Hot Wire Anemometer (HWA)
• CO2 tidal elimination (VTCO2)
method
Measuring range • 0 to 100 mmHg CO2 partial pressure
Parameters • Airway pressure
• 0 to 13.3 kPa CO2 partial pressure
• Airway flow
• 0 to 13.2 % CO2 volume (at a baro-
• Inspiratory and expiratory volumes
metric pressure of 1013 hPa)
• Trigger and End inspiration
System response time The total system response time of
Measuring • Flow: 0.12 to 32 l/min
CO2 the CO2 monitor when exposed first
range • Pressure: -40 to 120 cmH2O
to air and then to a gas mix with
Y sensor resis- 10 cmH2O/l/s at 30 l/min
5.0 % CO2 is <250 ms
tance
Warm-up time 15 s to initial CO2 indication maxi-
Dead space ≤1 ml
mum 2 minutes to full specification
Pressure line Gable mounted bulk head connector to fit
Oxygen concentration Automatic. Values supplied from the
connector tubing with an inner diameter of 3-4 mm
compensation ventilator system
(0.12–0.16")
Barometric pressure Automatic. Values supplied from the
Y sensor is recommended for conventional ventilation with
compensation ventilator system
small tidal volumes, and required during HFOV to get flow and
Digitizing rate 100 Hz
tidal volumes measurements.
Airway adapter dead • Neonatal/pediatric: <1 cm3
space
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10 GETINGE • SERVO -N
 Edi module (option) Communication / Interface

Edi module (option) Size Weight Serial ports • Isolated

Edi module W 154 x L 90 x H 21 mm
(W 6.1" x L 3.5" x H 0.8")
Edi catheter cable 2.0 m (6.6 ft)
Power source Powered by the ventilator
Power consumption <3 W during normal operation
Parameters • Edi waveform
• ECG leads waveforms
• NAVA estimated pressure waveform
(Pest)
• Two RS-232C ports. For data com-
0.25 kg
munication via the Servo Commu-
(0.6 lbs)
nication Interface (SCI).
-
Servo Communication A protocol for data communication
Interface (SCI) with external devices
Alarm output connec- • Isolated
tion (option) • 4-pin modular connector for com-
munication of all active alarms
• Switching capability: Max. 40 V DC,
max. 500 mA, max. 20 W

Data transfer via USB • Non-isolated

port • For transfer of trends, logs, screen-
shots and recordings to a USB
memory stick

Aerogen nebulizers Ethernet port • Isolated

• The network connection (LAN) port
Aerogen Pro Solo is for service use, and should only
nebulizers be used by personnel trained and
authorized by the manufacturer
Size W 50 x L 50 x H 45 mm W 48 x L 25 x H 67 mm
(W 2.0" x L 2.0" x H 1.8") (W 1.9" x L 1.0" x H 2.6") MSync, HL7 converter See separate datasheet
(optional)
Weight Approx. 25 g (0.88 oz) Approx. 14 g (0.49 oz)
VGA interface VGA connector for duplication of the
Particle size 1–5 µm mass median aerodynamic diameter
user interface
(MMAD)

Flow rate >0.2 (average: ~0.4) ml/min

Max. volume 10 ml 6 ml

Residual volume <0.1 ml for 3 ml dose

Control cable 1.8 m (5.9 ft)

Log function

Event log • Alarms

• Ventilator settings
• Apnea periods
• Immediate functions

Diagnostic log • Technical alarms

• Test results
• Service records
• Software installation
• Configuration information
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GETINGE • SERVO -N 11
 Saving of data Compressor Mini (option)

Recording of current 30 seconds of data will be recorded See separate datasheet

waveform and param- (15 seconds before and 15 seconds
eter values after activation). Up to 40 recordings
can be stored.

Saving screenshots Up to 40 screenshots can be stored.

Saving recruitments Up to 12 recruitments can be stored.

Service
Export files Recordings, screenshots , recruit-
Regular maintenance Preventive maintenance must be
ments and the event log can be
­performed by authorized personnel at
saved together in an export file and
least once every 5000 hours of
transferred to a USB memory stick.
­operation or once every 12 months,
whichever comes first.

Optional equipment

Optional Weight Dimensions Maxi-

equipment mum
load
Mobile cart 13.0 kg W 647 x L 547 x H 557 mm -
(28.7 lbs) (W 25.5" x L 21.5" x H 21.9")

Drawer for 0.6 kg W 247 x L 118 x H 302 mm -

mobile cart (1.3 lbs) (W 9.7" x L 4.6" x H 11.9")

Shelf base 2.5 kg W 207 x L 302 x H 43 mm -

(5.5 lbs) (W 8.2" x L 4.6" x H 1.7")

Pendant/bed 3.2 kg W 302 x L 302 x H 393 mm -

holder (7.1 lbs) (W 11.9" x L 11.9" x H 15.5")

Humidifier 0.5 kg W 243 x L 38 x H 185 mm 5 kg

holder (1.1 lbs) (W 9.6" x L 1.5" x H 7.3") (11.0
lbs)

Support arm 2.5 kg L 900 mm (35.4") 1–3 kg

178 (5.5 lbs) (2.2–6.6
lbs) *

* depending on angle

User inter- 0.6 kg W 46 x L 90 x H 123 mm -

face holder (1.3 lbs) (W 1.8" x L 3.5" x H 4.8")

Cable holder 0.1 kg W 138 x L 92 x H 155 mm 5 kg

for handle (0.2 lbs) (W 5.4" x L 3.6" x H 6.1") (11.0 lbs)
DocID:LAB-6888194 version:01 status: Approved

Waterbag/IV 0.4 kg W 148 x L 26 x H 1007 mm 1.5 kg

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pole (0.9 lbs) (W 5.8" x L 1.0" x H 39.6") (3.3 lbs)

Gas cylinder 0.5 kg Upper: Two 4.5

restrainer kit (1.1 lbs) W 104 x L 65 x H 48 mm liter
(W 4.1" x L 2.5" x H 1.9") bottles
Lower:
W 106 x L 162 x H 76 mm
(W 4.1" x L 6.4" x H 3.0")

Y piece W 26 x L 52 x H 46 mm
holder (W 1.0" x L 2.0" x H 1.8")

12 GETINGE • SERVO -N
 Ordering information
Servo-n, ventilator system and accessories:
See separate information in “System flowchart, Servo-n”
DocID:LAB-6888194 version:01 status: Approved
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GETINGE • SERVO -N 13
 Dimensional drawings
Servo-n on mobile cart Servo-n holder

Servo-n (patient unit) on Servo-n holder

DocID:LAB-6888194 version:01 status: Approved
2018-06-29 10:02 by Jennie Haag u2411101

14 GETINGE • SERVO -N
 DocID:LAB-6888194 version:01 status: Approved
2018-06-29 10:02 by Jennie Haag u2411101

Notes

GETINGE • SERVO -N
15
 © Maquet Critical Care AB 2018 · Servo-n, Automode, Open Lung Tool, Servo Compass, NAVA are trademarks by Maquet Critical Care AB · Subject to modifications · Order No. 68 88 194 Rev 01 · English · 2018-06
DocID:LAB-6888194 version:01 status: Approved
2018-06-29 10:02 by Jennie Haag u2411101

Getinge is a global provider of innovative solutions for operating rooms, intensive care units, sterilization departments and
for life science companies and institutions. Based on our firsthand experience and close partnerships with clinical experts,
healthcare professionals and medtech specialists, we are improving the everyday life for people, today and tomorrow.

Servo-n may be pending regulatory approvals to be marketed in your country. Contact your Getinge representative for
more information. This document is intended to provide information to an international audience outside of the US.

May be changed without prior notice.

Manufacturer · Maquet Critical Care AB · Röntgenvägen 2 SE-171 54 Solna · Sweden · +46 (0)10 335 73 00

www.getinge.com