SERVO-i v8.

0
Data sheet

This document is intended to provide information to an international audience outside of the US.
| 2 | SERVO-i v8.0 | Critical Care |

SERVO-i ventilator family

SERVO-i v8.0

SERVO-i configurations
®
The SERVO-i ventilator family consists of three configurations:
®
NIV NAVA
Infant NAVA
®

Nasal CPAP
Adult
NIV PC
Universal NIV PS
Y Sensor Measuring
CO2 Analyzer
Standard configuration
Nebulizer
Options Alarm output connection
Heliox
Not applicable STRESS INDEX
®
Open Lung Tool
®
The SERVO-i ventilator family addresses the very different Automode
requirements of neonatal, pediatric and adult needs from a single Bi-Vent/APRV
ventilation platform. The SERVO-i family can also be upgraded VS
with different options for future needs. The same ventilator can be
PRVC (incl. SIMV (PRVC) + PS)
used at the bedside, and in the MR-room* facilitating training,
VC (incl. SIMV (VC) + PS)
operation and maintenance, increasing efficiency and flexibility.
PC (incl. SIMV (PC) + PS)
*An agreement with Maquet must be signed, see conditions in the PS/CPAP
SERVO-i MR declaration (Order no. 66 71 670). All patient category software
Key to abbreviations

NAVA Neurally Adjusted Ventilatory Assist

NIV Non-invasive ventilation
SIMV Synchronized Intermittent Mandatory Ventilation
PRVC Pressure Regulated Volume Control
VS Volume Support
VC Volume Control
PS Pressure Support
PC Pressure Control
CPAP Continuous Positive Airway Pressure
 | Critical Care | SERVO-i v8.0 | 3 |

Technical specifications
SERVO-i v8.0

Intended use - general The system - general

The SERVO-i ventilator • Intended for treatment and The device complies with
system is: monitoring of patients in the requirements and
range of neonates, infants classification IIb of Medical
and adults with respiratory Device Directive 93/42/EEC.
failure or respiratory CE Mark Notified Body number:
insufficiency. 0123.
• The added indications for Classification: IEC 60601-1: 2005, Class I,
use of the NAVA option is continuous operation
when the electrical signal
from the brain to the Standards: • ISO 80601-2-12:2011
diaphragm is intact; NAVA • ISO 80601-2-55:2011
will improve synchrony
• EN 13544-1:2007+A1:2009
between the ventilator and
patients with no • IEC 60601-1, Type B
contraindication for (base unit, nebulizer patient
insertion/exchange of a unit with cable and the gas
Naso-Gastric tube. path ways)
• IEC 60601-1, Type BF
Instructions for use Please carefully read the user’s (CO2 analyzer)
manual
• IEC 60601-1, Type CF
Legal manufacturer Maquet Critical Care AB defibrillation proof
(Edi catheter and cable)
Other products See separate data sheets.
Contact your local Maquet A-weighted sound pressure <41 dB, measured at 1 m
supplier for more information. level (LpA) distance.

IP classification IP 21
Electromagnetic compatibility According to limits specified in
(EMC): IEC 60601-1-2:2007.
The 'EMC Declaration, Information to the Responsible
Organization' is available from Maquet.

Patient range: Weight:

• Adult, all ventilation modes: 10 - 250 kg
• Infant, invasive ventilation: 0.5 - 30 kg
• Infant, NAVA + NIV NAVA: 0.5 - 30 kg
• Infant, NIV PS+PC: 3 – 30 kg
• Infant, Nasal CPAP: 0.5 – 10 kg
| 4 | SERVO-i v8.0 | Critical Care |

Technical specifications
SERVO-i v8.0

Operating conditions Power supply

Operating temperature: +10 to +40ºC Power supply, automatic range 100 – 120 V AC ±10%, 50 –
selection: 60 Hz, or 220 – 240 V AC ±10%,
Relative humidity: 15 to 95% non-condensing 50 – 60 Hz.
Atmospheric pressure: 660 to 1060 hPa Plug-in battery module:
Lowest pressure in breathing –400 cmH2O • Battery backup: Two battery modules are
system: delivered with the ventilator. Up
to six battery modules can be
included.
Non-operating conditions • Battery capacity: Rechargable, 12 V, 3.5 Ah each.
Impact: • Peak acceleration: 15 g. • Recharge time: Approximately 3 h/battery.
• Pulse duration: 6 ms.
• Battery backup time: At least 3 h, when using six
• Number of impacts: 1000. batteries.
Storage temperature: –25 to +60º C (–13 to 140º F)
External 12 V DC: 12.0 V – 15.0 V DC, 10 A
Storage relative humidity: < 95%
Max power consumption: At 100 – 120 V: 2 A, 190 VA,
Storage atmospheric pressure: 470 to 1060 hPa
140 W.
At 220 – 240 V: 1 A, 190 VA,
140 W.
 | Critical Care | SERVO-i v8.0 | 5 |

Technical specifications
SERVO-i v8.0

The ventilator - general User interface

Dimensions: (See dimensional drawings Weight: Approximately 5 kg
page 15)
Attachment: Can be attached to the mobile
• User interface: W 355 x D 53 x H 295 mm cart, a table, rail or pole (15 –
• Patient unit: W 300 x D 205 x H 415 mm 30 mm diameter).

Weight: Approximately 20 kg (Patient

Unit 15 kg, User Interface 5 kg)
Screen
Method of triggering: Flow, pressure and Edi Type: TFT-LCD module
(optional)
Size: 31 cm (12.1”) diagonal
Max. operating pressure: Approximately 115 cmH2O
Viewing area: 246.0 x 184.5 mm
Bias flow:
• Adult: 2 l/min
• Infant: 0.5 l/min Inspiratory channel
Pressure drop: Max. 6 cmH2O at a flow of 1 l/s

Internal compressible factor: Max. 0.1 ml/cmH2O

Gas supply
Gas delivery system: Microprocessor controlled valve
Inlet gas pressure Air/O2: 200 – 600 kPa / 2.0 – 6.0 bar /
29 – 87 PSI Inspiratory flow range:
Connection standards available: AGA, DISS, NIST, or French • Adult: 0 – 3.3 l/s
standard.
• Infant: 0 – 0.55 l/s
Unavailable gas/loss of gas The flow from an unavailable
pressure: gas (air or O2) is automatically
compensated for so that the
patient gets the preset volume
and pressure. Expiratory channel
Pressure drop: Max. 3 cmH2O at a flow of 1 l/s

Internal compressible factor: Max. 0.1 ml/cmH2O

Patient system gas connectors
PEEP regulation: Microprocessor controlled valve
Conical fittings: Male 22 mm / female 15 mm. In
accordance with ISO 5356-1. Rise time, expiratory flow <12 ms for 10 – 90 % response
measurement: at flow of 0.05 – 3.2 l/s
Gas exhaust port: Male 30 mm cone
Expiratory flow range: 0 to 3.2 l/s
| 6 | SERVO-i v8.0 | Critical Care |

Technical specifications
SERVO-i v8.0

Alarms Alarms
Airway pressure (upper): Battery: • Limited battery capacity:
10 min.
• Adult, Invasive ventilation 16 – 120 cmH2O
• No battery capacity: less
• Adult, Non-invasive 16 - 70 cmH2O than 3 min.
ventilation • Low battery voltage.
• Infant, Invasive ventilation: 16 – 90 cmH2O
End-tidal CO2 (upper and lower • 0.5 – 20%.
• Infant, Non-invasive 16 - 70 cmH2O limit): • 4 – 100 mm Hg.
ventilation
• 0.5 – 14 kPa.
Expired minute volume (Upper
alarm limit): Leakage out of range in NIV: Yes. Described in the User’s
manual.
• Adult: 0.5 – 60 l/min
• Infant: 0.01 – 30 l/min Technical: Yes. Described in the User’s
manual.
Expired minute volume (Lower
alarm limit): Autoset (alarm limits) Invasive ventilation, controlled
specification: modes only.
• Adult: 0.5 – 40 l/min
• High airway pressure: Mean peak pressure
• Infant: 0.01 – 20 l/min +10 cmH2O or at least
35 cmH2O.
It is possible to permanently silence this alarm (an option with
infant version only) • Upper minute volume: Expiratory minute volume
+ 50%.
No patient effort (Apnea) alarm • Lower minute volume: Expiratory minute volume
• Adult: 15 – 45 s – 50%.
• Upper respiratory frequency: Breathing frequency + 40%.
• Infant 1 - 45 s
• Lower respiratory frequency: Breathing frequency – 40%.
Automatic return to support mode on patient triggering
• High end expiratory pressure: Mean end expiratory pressure
No consistent patient effort: Yes, described in User's manual + 5 cmH2O.
Respiratory frequency: 1 – 160 breaths/min • Low end expiratory pressure: Mean end expiratory pressure
– 3 cmH2O.
High end expiratory pressure: 0 – 55 cmH2O
• Upper end tidal carbon End tidal carbon dioxide
Low end expiratory pressure: 0 – 47 cmH2O. dioxide concentration concentration + 25%.
(etCO2):
Note. Setting the alarm to 0
(zero) is equal to alarm off. • Lower end tidal carbon End tidal carbon dioxide
dioxide concentration concentration – 25%.
High continuous pressure: Obstruction leading to constant (etCO2):
high airway pressure (>PEEP
+15 cmH2O) during: > 2 breaths
or 5 seconds, whichever is
greater, 15 ±1.5 s if less than 2
breaths are triggered
O2 concentration: Set value ±5 vol% or ≤18 vol%

Gas supply: Below 200 kPa / 2.0 bar /

29 PSI and above 600 kPa /
6.0 bar / 87 PSI
 | Critical Care | SERVO-i v8.0 | 7 |

Technical specifications
SERVO-i v8.0

Ventilation modes – Invasive ventilation Ventilation modes – Non-invasive ventilation (optional)

Controlled ventilation: NIV PC
• PC NIV PS
• VC Can be configured with Nasal CPAP
alternative flow patterns
- VC with flow adaptation,
- VC without flow adaptation,
- VC with decelerating flow Ventilation modes - NAVA (optional)
• PRVC NAVA Neurally Adjusted Ventilatory
Assist via endotracheal tube or
tracheostomy
Supported ventilation:
• PS/CPAP NIV NAVA Neurally Adjusted Ventilatory
Assist via non-invasive patient
• VS Optional with Infant and Adult interfaces

Combined ventilation:
• SIMV (VC) + PS: Comes with the corresponding Waveform and loop presentations
controlled ventilation mode Real time waveforms - up to 4 waveforms can be displayed
• SIMV (PC) + PS: Comes with the corresponding simultaneously:
controlled ventilation mode • Pressure
• SIMV (PRVC) + PS Comes with the corresponding • Flow
controlled ventilation mode • Volume
• Bi-Vent/APRV Pressure controlled ventilation • CO2 Requires SERVO-i CO2 Analyzer
on two independently adjustable option
levels, allowing unrestricted
spontaneous breathing on both • Edi Requires SERVO-i NAVA option
levels. (Optional with Infant and
Adult) Loops:
• Volume / Pressure* *A reference loop and three
Automode • Control mode: VC <—> overlaying loops can be
Support mode: VS displayed.
• Control mode: PC <—>
Support mode: PS • Flow / Volume* *Displayed simultaneously with
Open Lung Tool graphical
• Control mode: PRVC <—> trends, if requested.
Support mode: VS
• (Optional)
| 8 | SERVO-i v8.0 | Critical Care |

Technical specifications
SERVO-i v8.0

Displayed Trended Displayed Trended

Monitoring Monitoring
value value* value value*
Breathing frequency: Yes Yes STRESS INDEX: Yes Yes
Spontaneous breaths per No Yes Inspiratory resistance: Yes Yes
minute (RRsp):
Expiratory resistance: Yes Yes
Peak airway pressure: Yes Yes
Elastance: Yes Yes
Mean airway pressure: Yes Yes
Time constant: Yes No
Pause airway pressure: Yes Yes
P0.1: Yes Yes
End expiratory pressure: Yes Yes
Work of breathing patient: Yes Yes
CPAP pressure: Yes Yes
Work of breathing ventilator Yes Yes
Inspired tidal volume: Yes Yes
Shallow Breathing Index (SBI): Yes Yes
Expired tidal volume: Yes Yes
Supply pressure (O2 and air): Yes No
Inspired minute volume: Yes Yes
Battery remaining time: Yes No
Expired minute volume: Yes Yes
Barometric pressure: Yes No
Leakage fraction in NIV (%): Yes Yes
*Stored trend values for up to 24 hours
Ti/Ttot: Yes No
I:E ratio: Yes No
Log function
Total PEEP: Yes No
Event log: • Alarms.
Edi peak: Yes Yes • Ventilator settings.
Edi min: Yes Yes • Apnea periods.
• Immediate functions.
Switch to backup (b/min) No Yes
Service log: • Technical alarms.
Backup (%/min) No Yes
• Test results.
O2 concentration (measured): Yes Yes • Preventive maintenance.
CO2 end tidal concentration Yes Yes • Service history.
(etCO2): • Configuration log.
CO2 minute elimination (CO2): Yes Yes

Tidal CO2 elimination (VTCO2): Yes Yes

MVe sp / MVe: Yes No

Spontaneous exp. minute Yes Yes

volume (MVe sp):

End expiratory flow: Yes Yes

Static compliance: Yes Yes
Dynamic compliance: Yes Yes
 | Critical Care | SERVO-i v8.0 | 9 |

Technical specifications
SERVO-i v8.0

Parameter settings Setting range: Parameter settings Setting range:

Parameter: Infant Adult Parameter: Infant Adult
Inspiratory tidal volume (ml): 2 – 350 100 – 4000 End inspiration (% of peak flow): 1 – 70 1 – 70
Inspiratory minute volume 0.3 – 20 0.5 – 60 End inspiration in NIV (% of 10 – 70 10 – 70
(l/min): peak flow):
Apnea, time to alarm (s): 1 - 45 15 – 45
Automode trigger timeout (s): 3 – 15 7 – 12 Backup settings Setting range:
PC/PS above PEEP (cmH2O) 0 – (80 -PEEP) 0 – (120 Parameter: Infant Adult
-PEEP) Inspiratory tidal volume (ml): 2 – 350 100 – 4000
PC/PS above PEEP in NIV 0 - (62 - PEEP) 0 - (62 - PEEP) PC above PEEP (cmH2O) 5 – (80 -PEEP) 5 – (120
(cmH2O) -PEEP)
PEEP (cmH2O) 0 – 50 0 – 50 PC above PEEP in NIV 5 - (62 PEEP) 5 - (62 PEEP)

PEEP in NIV (cmH2O) 2 – 20 2 – 20 CMV frequency (breaths/min): 4 – 150 4 – 150

CPAP pressure (cmH2O): 2 – 20 – I:E ratio: 1:10 – 4:1 1:10 – 4:1

CMV frequency (breaths/min): 4 – 150 4 – 150 TInsp (s): 0.1 – 5 0.1 – 5

SIMV frequency (breaths/min): 1 – 60 1 – 60

Breath cycle time, SIMV (s): 0.5 – 15 1 – 15 Non-invasive ventilation (optional)
PHigh (cmH2O) (PEEP + 1) – 50 (PEEP + 1) – 50 Leakage compensation level
• Adult: Inspiratory, up to 200 l/min
THigh (s): 0.2 - 30 s 0.2 - 30 s
Expiratory, up to 65 l/min
TPEEP (s): 0.1 - 10 s 0.1 - 10 s • Infant: Inspiratory, up to 33 l/min
PS above PHigh (cmH2O): 0 – (80 - PHigh) 0 – (120 - PHigh) Expiratory, up to 25 l/min
• Infant, Nasal CPAP: up to 20 l/min
O2 concentration (%): 21 – 100 21 – 100
Leakage overrange detection: Automatic
I:E ratio: 1:10 – 4:1 1:10 – 4:1
Disconnect detection: Automatic
TInsp (s): 0.1 – 5 0.1 – 5
Disconnect flow: Configurable
NAVA level (cmH2O/µV): 0 - 15 0 - 15
• Low 7.5 l/min
Edi trigger sensitivity (µV): 0.1 – 2.0 0.1 – 2.0 • High - 40 l/min (Adult)
TPause (s): 0 – 1.5 0 – 1.5 - 15 l/min (Infant)

TPause (% of breath cycle time): 0 – 30 0 – 30 • Disabled Deactivates disconnect

detection
Flow trigger sensitivity level: 0 – 10 0 – 10
Connect detection: Manual, or automatic via bias
Press. trigg sensitivity (cmH2O): -20 – 0 -20 – 0 flow
Insp. rise time (% of breath 0 – 20 0 – 20
cycle time):
Insp. rise time (s): 0 – 0.2 0 – 0.4
| 10 | SERVO-i v8.0 | Critical Care |

Technical specifications
SERVO-i v8.0

Open Lung Tool (OLT) (optional) Parameter: Setting range

Three simultaneous graphical 1. EIP and PEEP (End Oxygen breaths: 100% for 1 minute
trends, presented Inspiratory Pressure and
breath-by-breath: Positive End Expiratory Start breath: Initiation of 1 breath (In SIMV
pressure). mode initiation of 1 mandatory
breath)
2. VTi and VTe (Inspiratory and
Expiratory Tidal volume). Pause hold: Insp. or exp (0 – 30 seconds)

3. C dyn i and VTCO2* Alarm silence/reset: 2 minute silence and reset of

latched alarms
(Dynamic inspiratory
Compliance [= VTi/(EIP – PEEP)] Compliance compensation: On/Off
and Tidal CO2 elimination*).
Automode (optional): Automode On/Off
* Requires SERVO-i CO2
Nebulizer (optional): 5 - 30 min./Continuous/Off
Analyzer option.
Backup ventilation: Backup On/Off
Values stored breath by breath: Up to 21.600 breaths.
Cursor function: A cursor can be moved with the Suction support
main rotary dial or via the touch
screen. When moving it along Pre oxygenation time: Max. 2 min
the graph, the numeric Post oxygenation time: Max. 1 min
parameter values valid for that
actual moment will be shown. Suction phase time: No maximum level
Zoom function: Time resolution of the x-axis Adjustable oxygen level: 21 – 100 %
can be selected in five different
steps.
Time marking: Hours and minutes (when values
are measured).
 | Critical Care | SERVO-i v8.0 | 11 |

Technical specifications
SERVO-i v8.0

STRESS INDEX (optional) Saving of data

Presented values: • SI (STRESS INDEX) Recording of current waveform 20 seconds of data will be
• PEEP (Positive End and parameter values: recorded (10 seconds before
Expiratory pressure). and 10 seconds after
activation).
• VTe (Expiratory Tidal volume).

Stored values: • 120 values stored in graph

• Stored trend values up to 24 NAVA (optional)
hours
Size:
Cursor function: A cursor can be moved with the • Edi module: 154 x 90 x 21 mm
main rotary dial. When moving
it along the graph, the numeric • Edi catheter cable: Length: 2 m
parameter values valid for that
actual moment will be shown. Weight - Edi module: 0.25 kg

Time marking: Hours and minutes (when values Power source - Edi module Powered from SERVO-i. <3 W
are measured). supply voltage: at 12 V (normal operation)
Parameters: • Edi waveform
• ECG leads waveforms
Communication/interface
• NAVA estimated pressure
Serial ports (2): RS-232C - isolated. For data waveform (Pest)
communication via the
Communication Interface Edi catheters: • 6 Fr, length 49 cm
Emulator (CIE). • 8 Fr, length 50 cm
Alarm output connector (optional) • 6 Fr, length 50 cm
• 8 Fr, length 100 cm
Connector: 4-pole Modular connector
• 8 Fr, length 125 cm
Ratings: Max 40 V DC, Max 500 mA,
• 12 Fr, length 125 cm
Max 20 W
• 16 Fr, length 125 cm

Data transfer (optional): Via Ventilation Record Card

Screen picture transfer Via Ventilation Record Card
(optional)
| 12 | SERVO-i v8.0 | Critical Care |

Technical specifications
SERVO-i v8.0

SERVO-i CO2 analyzer (optional) SERVO-i CO2 analyzer – performance

Size: Measuring method: Mainstream, dual-wavelength,
non-dispersive infrared.
• CO2 analyzer module: 154 x 90 x 43 mm
Parameters: • Capnogram.
• Sensor: 32.0 x 47.0 x 21.6 mm
• CO2 End tidal concentration
(etCO2).
Weight:
• CO2 Minute elimination
• CO2 analyzer module: 450 g ( CO2).
• Sensor: 20 g • Tidal CO2 elimination
• Airway adapter: 10 g (VTCO2).

Measuring range: • 0 to 100 mmHg CO2 partial

Connectors and cables: pressure.
• 0 to 13.3 kPa CO2 partial
• Sensor cable: 2.8 m
pressure.
• 0 to 13.2% CO2 volume (at a
Operating conditions barometric pressure of
• Operating temperature:
o o
+10 C to + 33 C 1013 hPa).
System response time CO2 The total system response time
of the CO2 monitor when
exposed first to air and then to
a gas mix with 5.0 % CO2 is
<250 ms.
Warm-up time: 15 s to initial CO2 indication,
maximum 2 minutes to full
specification
Oxygen concentration Automatic. Values supplied from
compensation: the SERVO-i Ventilator System.
Barometric pressure Automatic. Values supplied from
compensation: the SERVO-i Ventilator System.
Digitizing rate: 100 Hz
Airway adapter dead space:
• Adult: <5 ml
• Infant: <1 ml
 | Critical Care | SERVO-i v8.0 | 13 |

Technical specifications
SERVO-i v8.0

Y sensor measuring (optional) Aerogen nebulizer systems (optional)

Size: Weight - Aerogen module: Approx. 216 g
• Y sensor module: 154 x 90 x 43 mm Dimensions - Aerogen module: H 105 mm x L 108 mm x
• Y sensor adult: Length 84 mm W 60 mm

• Y sensor infant: Length 51 mm Connection cable length: 2.0 m

Weight: Particle size: 1 - 5 µm mass median

aerodynamic diameter (MMAD)
• Y sensor module: 0.4 kg
Flow rate: >0.2 ml/min
• Y sensor adult: 10.5 g
Volume - nebulizer unit • Pro - 10 ml
• Y sensor infant: 7.5 g
• Solo - 6 ml
Sensor material: Makrolon polycarbonate.
Residual volume: 10 %
Tubing: 2.0 m. Medical grade PVC.
Power source – Y sensor Powered from the SERVO-i.
module supply voltage: <5 W at 12 V (normal operation). SERVO-i Mobile cart (optional)
Weight: 21 kg
Dimensions: H 992 mm x L 640 mm x
Y Sensor measuring – performance
W 560 mm
Measuring method: Fixed orifice, differential (see dimensional drawing
pressure. below)
Parameters: Airway pressure

Airway flow SERVO-i Drawer kit (optional)

Inspiratory and expiratory Weight: 4.5 kg
volumes Dimensions: H 240 mm x L 210 mm x
W 300 mm
Measuring range:
• Adult: 2 to 180 l/min
SERVO-i Holder (optional)
• Infant: 0.125 to 40 l/min
Weight: 3.5 kg
Airway adapter dead space:
Dimensions: H 352 mm x L 247 mm x
• Adult: < 9.0 ml W 159 mm
• Infant: < 0.45 ml (see dimensional drawing
below)

SERVO-i Shelf base (optional)

Weight: 1.2 kg
Dimensions: H 29 mm x L 205 mm x
W 159 mm
(see dimensional drawing
below)
| 14 | SERVO-i v8.0 | Critical Care |

Technical specifications
SERVO-i v8.0

Gas cylinder restrainer (optional) Compressor Mini (optional)

Max load: 2 x 5-liter bottles See separate data sheet.

SERVO-i IV pole (optional) Service

Max load (total): 6 kg Regular maintenance: Once every 12 months or at
least after 5000 operating hours.

Gas trolley (optional)

Note
Max load: 2x10 kg bottles
For inaccuracies and more detailed technical specifications please
Docking: Dockable to SERVO-i Mobile refer to the User’s manual.
cart.
Dockable to a separate wall
clamp.
Ordering information

SERVO-i, Ventilator and accessories: See separate information:

“SERVO-i System Flow Chart” (Order no: 66 70 102).
 | Critical Care | SERVO-i v8.0 | 15 |

Technical specifications
SERVO-i v8.0

Dimensional drawings

SERVO-i on Mobile cart SERVO-i Holder

1292 mm
992 mm

SERVO-i (patient unit) on SERVO-i Holder

SERVO-i Shelf base

 © Maquet Critical Care AB 2016. All rights reserved. • Maquet reserves the right to modify the design and specifications contained herein without prior notice.
Products may be pending regulatory approvals to be marketed in
your country. Contact your Maquet representative for more
information.
This document is intended to provide information to an international

Order No. 66 70 105 • Data sheet • Printed in Sweden • 160411• Rev: 22 English •
audience outside of the US.

Manufactured: Maquet Critical Care AB

Röntgenvägen 2
171 54 Solna, Sweden
Phone: +46 (0) 10 335 73 00

www.maquet.com

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