Philips NOCTN96 452299122601 User Manual Specification Sheet Respironics Non Invasive Ventilator V60 Cf78d964bbf043ab953aa77c01435e39

User Manual: Philips NOCTN96 Specification Sheet Philips Respironics Non-invasive ventilator V60 Respironics V60 Non-invasive ventilatorNOCTN96

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Hospital
respiratory care
V60 ventilator
Specifications

Dedicated to
successful NIV
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Specifications

1. Patient types

The Philips Respironics V60 ventilator
combines Respironics’ ventilation
expertise with Philips focus on
simplifying advanced health care.
The result is exceptional noninvasive
ventilation with an invasive ventilation
fallback and an interactive display that
helps simplify patient management.

Adult
Pediatric (≥20kg)

2. Modes
Standard
CPAP (continuous positive airway pressure)
S/T (spontaneous with timed backup)
PCV (pressure control ventilation)
AVAPS (average volume assured pressure support)
Optional
PPV (proportional pressure ventilation)*

3. Settings
Settings

Range

C-Flex

OFF, 1 – 3

CPAP

4 – 25cmH2O

EPAP

4 – 25cmH2O

IPAP

4 – 40cmH2O

I-time (inspiratory time)

0.30 – 3.00sec

Max P (AVAPS maximum IPAP)

6 – 40cmH2O

Min P (AVAPS minimum IPAP)

5 – 30cmH2O

O2 (oxygen percent)

21 – 100%

Ramp time

OFF, 5 – 45min

Rate (respiratory rate)

4 – 60bpm

Rise (rise time)

1–5

Triggering and cycling

Auto-adaptive (AutoTrak)

AVAPS target tidal volume

200 – 2,000ml btps

Max E

0 – 100cmH2O/I

Max R

0 – 50cmH2O/l/s

PPV%

0 – 100%

Max P (PPV maximum pressure limit)

5 – 40cmH2O

Max V (PPV maximum volume limit)

200 – 3,500ml

* May not be available in all markets

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6. Alarms

4. Modes with settings

Alarm

Adjustable range

Rate

Hi Rate (high respiratory rate alarm)

5 – 90bpm

I-time

Lo Rate (low respiratory rate alarm)

1 – 89bpm

CPAP

Hi V T (high tidal volume alarm)

200 – 3,500ml

EPAP

Lo V T (low tidal volume alarm)

Off, 5 – 1,500ml

IPAP

HIP (high inspiratory pressure alarm) 5 – 50cmH2O

Rise

LIP (low inspiratory pressure alarm)

OFF, 1 – 40cmH2O

Min P

Lo VE (low minute ventilation alarm)

OFF, 0.1 – 99l/min

Max P

LIP T (low inspiratory pressure
delay time)

5 – 60sec

CPAP

S/T

PCV

AVAPS

PPV

Max V
Max E

7. Other settings

Max R

Alarm volume

1 – 10 (relative scale)

Brightness

1 – 5 (relative scale)

Exhalation port selection

•	 DEP (disposable
exhalation port)
•	 Whisper Swivel
•	 PEV (plateau exhalation
valve)
•	Other
•	 None (no inline circuit
exhalation port)

5. Monitored parameters

Interface selection

ET/Trach, 1, 2, 3, Other

Patient data window

Screen lock

Off, On

PPV%
O2
V T (tidal volume)
C-Flex
Ramp time

Breath phase/trigger indicator

Spont, timed, exhale

Auto-Trak Plus

Optional*

PIP

0 – 50cmH2O

Trigger*

Normal, 1 – 7

Patient/total leak

0 – 200l/min btps

E-cycle*

-2, -1, Normal, 1 – 6

Patient trigger

0 – 100%

Respiratory rate

0 – 90bpm

8. Environmental

Ti/Ttot

0 – 91%

Temperature

Minute volume

0 – 99.0l/min btps

Operating conditions

+5 – +40ºC

Tidal volume

0 – 3,500ml btps

Storage conditions

-20 – +50ºC

Waveform window

Relative humidity

Pressure waveform

0 – 50cmH2O

Operating conditions

15 – 95% (non-condensing)

Flow waveform

-240 – 240l/min btps

Storage conditions

10 – 95% (non-condensing)

Volume waveform

0 – 3,500ml btps

Barometric pressure
Operation and storage

79.9 – 101.1kPa
(600 – 765mmHg)

Altitude
Operation and storage

* May not be available in all markets

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600 to 765 mmHg
(approximately -61 to
1951m (-200 to 6400 ft)
relative to sea level)

9. Communication

EN 61000-4-3

Radiated Electromagnetic Field Immunity
Test (10V/M)

EN 61000-4-4

Electrical Fast Transient/Burst Immunity Test

EN 61000-4-5

Surge Immunity Test

EN 61000-4-6

Immunity to Conducted RF Disturbances
(10V)

EN 61000-4-8

Power Frequency Magnetic Field Immunity
Test

EN 61000-4-11

Voltage Dips, Short Interruptions, and
Voltage Variations Immunity Tests

MIL-STD 461E
RE101

Electromagnetic Field Generation (Army
Level)

ANSI/AAMI ES
60601-1

Medical electrical equipment - Part 1:
General requirements for basic safety and
essential performance

WEEE recycling
directive	

Compliant with the WEEE recycling directive

Philips IntelliBridge EC10
Philips IntelliBridge EC40/80
Philips VueLink Open Interface
Respi-Link remote diagnostic system
Bernoulli® management system
Capsule DataCaptorTM device interface driver
GE Healthcare (Centricty Critical Care)
Cerner CareAware® iBus™
Other monitoring and patient information systems
RS232 digital and analog
10. Electrical
External
AC voltage

100 – 240 VAC

AC frequency

50/60Hz

AC power

300 VA

IEC 60601-1;
Ed. 3.1

Medical electrical equipment – Part 1:
General requirements form basic safety and
essential performance

Nominal voltage

14.4V

Capacity

11.0Ah

IEC 60601-1-2;
Ed. 3.0

Battery chemistry

Lithium-ion

Medical electrical equipment - Part 1-2:
General requirements for basic safety and
essential performance - Collateral Standard:
Electromagnetic disturbances

Operating time

6 hours in normal conditions

IEC 60601-1-6;
2013

Medical electrical equipment – Part 1-6:
General requirements for safety

IEC 60601-1-8;
Ed. 2.1

Medical electrical equipment – Part 1-8:
General requirements for safety

3rd edition standards

Battery (optional)

11. Physical
Weight

11.7kg (25.7lb) with optional battery
10.6kg (23.3lb) without optional battery

IEC 62366;
2007 + A1: 2004

Medical devices - Application of usability
engineering to medical devices

Dimensions

33.7cm (13.3in) height
39.4cm (15.5in) width
42.9cm (16.5in) depth

ISO 14971;
2007

Medical devices – Application of risk
management to medical devices

EN ISO 14971;
2012

Medical devices – Application of risk
management to medical devices

ISO 80601-2-12;
2011

Medical electrical equipment – Particular
requirements for basic safety and essential
performance of critical care ventilators

ISO 60529;
Ed. 2.1

Degrees of protection provided by
enclosures (IPX1 @ 0° tilt)

IEC 62304;
Ed. 1.0

Medical device software - Software life cycle
processes

ANSI/AAMI ES
60601-1	

Medical electrical equipment - Part 1:
General requirements for basic safety and
essential performance

WEEE recycling
directive

Compliant with the WEEE recycling directive

12. Regulatory compliance
2nd edition standards
EN 60601-1-2

Electromagnetic Compatibility Requirements
and Tests

EN 55011

Radiated and Conducted RF Disturbance
Characteristics--Limits and Methods of
Measurement (Level A)

EN 55014-1

Electromagnetic Compatibility
Requirements. Part 1: Emissions

EN 61000-3-2

Limits for Harmonic Current Emissions

EN 61000-3-3

Limitation of Voltage Changes, Fluctuations,
and Flicker Emissions

EN 61000-4-2

Electrostatic Discharge Immunity Test (8/15KV)

Please visit www.philips.com/V60

© 2016 Koninklijke Philips N.V. All rights reserved.
Specifications are subject to change without notice.

Bernoulli is a registered trademark of Cardiopulmonary Corp.
DataCaptor is a trademark of CapsuleTech.
CareAware, and iBusare trademarks of Cerner Corp.

www.philips.com
4522 991 22601 * OCT 2016

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