NEW LUCAS 3

Chest Compression System, version 3.1

Data Sheet

Setting the standard

for mechanical CPR
We continue to innovate the LUCAS
platform with Wi-Fi® connection
to the LIFENET® System and
integration into CODE-STAT™
Data Review Software. The new
LUCAS 3, v3.1, allows for tailored
rates to meet your protocols, alerts
configured to improve compliance,
Post-Event Reports to your inbox,
and asset notifications by e-mail.

Device configuration via the LIFENET System The world’s most used mechanical CPR device
Wirelessly set device presets to align with your protocols • Over 15 years of experience, over 24,000 devices
• Adjustable rate: 102, 111, 120 ± 2 compressions per deployed, and 200+ publications**
minute – fixed or variable during operation • Unique device design: piston with suction cup designed
• Adjustable depth: 1.8 to 2.1 ± 0.1 inches/45 to to stabilize the compression point and follow the chest
53 ± 2mm – fixed during operation • Used in the field all the way into the cardiac cath lab
• Audible CPR timer: 1-15 minutes (in 1 minute increments)
Proven safe and effective, quick and easy
• Adjustable ventilation alerts, pause length and count
• Highest level of evidence showing safety and efficacy1
• Auto-lowering of the piston (AutoFit or QuickFit)
• Simple 1-2-3 step user interface
• Pressure pad release to allow for chest rise
• Quick: A median 7 sec. interruption at transition from
during ventilation
manual to mechanical CPR in clinical use2
Post-Event reporting
Proven to perform. Reliably.
• Receive device Post-Event Report (PDF) via e-mail
• Easy to maintain and own
after device check-in over Wi-Fi
• Compact and lightweight
• Transmit reports wirelessly to any predetermined
e-mail addresses (configurable in LIFENET) • >99% operational reliability in clinical use1
• Integration with CODE-STAT 11*

Asset management via LIFENET

• Asset dashboard for fleet status at latest device check-in
• Notifications of expiring and expired LUCAS batteries
• Notifications of upcoming or missed service

*Commercially available mid-2018

**As of April 2018
LUCAS 3 Chest Compression System

Specifications

Device post-event data

Device and Therapy Device and Therapy (cont.) and connectivity

Type of chest compression Suction cup start position Connectivity

• Piston with suction cup designed to • Configurable: • Wireless connectivity: Device can
stabilize the compression point -- QuickFit (factory default setting): communicate via Bluetooth™ (factory
• Factory default settings consistent Manual lowering of the suction cup. default setting ON) and connect to
with AHA and ERC Guidelines 2015 Automatic fine-tuning will occur configured Wi-Fi networks to receive
when locking the start position and transmit data when not in
Compression rate
-- AutoFit: Automatic lowering of the clinical use.
• Configurable to 102 – 111 – 120
suction cup from its upper position • Local Bluetooth connection for setting
compressions per minute, fixed, or
down to the chest up local Wi-Fi network, and for Post-
variable during use
-- Manual: Manual lowering of Event Report generation and software
• Factory default setting: 102 ± 2 updates (if Wi-Fi cannot be used)
compressions per minute the suction cup to the chest. No
automatic fine-tuning will occur • Ability to disable Bluetooth and/
Compression depth when locking the start position or Wi-Fi
• Configurable to a fixed value Wi-Fi and LIFENET capabilities
Suction cup in ADJUST mode: The
between 1.8 to 2.1 ± 0.1 inches /
device can be setup so that the suction • Manual or automatic data transmission
45 to 53 ± 2 mm
cup automatically returns up from the (configurable): push the TRANSMIT
• Factory default setting: chest when the operator pushes the key in range of known network (factory
2.1 ± 0.1 inches / 53 ± 2 mm for ADJUST key coming from PAUSE or default setting), or setup option for
nominal patients ACTIVE (30:2 or Continuous) modes automatic data transmission whenever
Note: 1.5 to 2.1 inches / 40 to 53 mm (factory default setting: OFF) the device is off, charging and in range
for chest height < 7.3 inches / 185 mm of known network
Audible timers
Pressure pad during ventilation • Setup options: Device functionality
• 1 to 15 minutes, in 1 minute increments
• To allow for chest rise during (factory default setting: OFF) can be configured with setup options
ventilation the pressure pad can be via secure, online platform (LIFENET)
• The timer can be setup as either CPR
configured to move up 0.4 inch / 10 mm and be transmitted to the device
Timer or Continuous Timer
above start position during pauses or wirelessly. A single setup profile can
during continuous compressions -- CPR Timer: the device only be applied to entire fleet or individual
measures the time in uninterrupted setup options for each device
• Factory default setting: pressure pad
ACTIVE (30:2 or Continuous) modes
remains in start position • Post-Event Reports: Device can
-- Continuous Timer: the device transmit Post-Event Reports
Compression duty cycle: 50 ± 5% measures the time continuously, (PDF) wirelessly and send to any
Compression modes (operator independent of what mode the predetermined e-mail addresses.
selectable) device is in
• Device readiness status: Device
• ACTIVE 30:2 mode: 30:2 (factory Safety system controls can transmit device readiness and
default setting) or 50:2 (setup option) • Automatic self-test at each Power ON battery notifications wirelessly to any
compression to ventilation ratio predetermined e-mail addresses
• Advanced control of delivered
• ACTIVE Continuous mode compression depth, rate and duty Post-Event Report contents: Easy to
Ventilation alerts cycle, with safety alarm read Post-Event Report (PDF) showing:
• ACTIVE 30:2 mode: LED blinks • Soft Start at beginning of • Summary of device use: compression
and audible alert signals before compressions time, ratio, rate, count, number of
ventilation pause • Automatic adjustment of compression pauses > 10 sec. and duration of
• ACTIVE Continuous mode: LED force to reach the set compression longest compression pause
blink. Configurable to 6 to 10 alerts depth in individual chests • Visual timeline showing device
per minute (factory default setting: Patients eligible for treatment compressions, rate and pauses
10 alerts per minute). Audible alert • Event log showing user interactions,
• 6.7 to 11.9 inches / 17.0 to 30.3 cm
configurable ON/OFF (factory default battery alerts and alarms
chest height
setting: OFF) • Full display of device setup for
• 17.7 inches / 44.9 cm maximum
Ventilation pause duration chest width quick reference
• ACTIVE 30:2 mode: configurable to • No patient weight limitation • Comprehensive post-event review in
3 to 5 sec. (factory default setting: CODE-STAT 11 Data Review Software
3 sec.) (optional)
• ACTIVE Continuous mode:
configurable to 0.3 to 2 sec.
(factory default setting: 0.3 sec.)
Device post-event data Device environmental
and connectivity (cont.) specifications Power specifications (cont.)

Device readiness data: Configurable in Operating temperature Maximum Battery charge time:
LIFENET to send e-mail notifications on • +32°F to +104°F / +0°C to +40°C Charged in the device using external
latest device check-in status including: • -4°F / -20°C for 1 hour after storage at power supply:
• Battery nearing expiration room temperature • Less than two hours at room
• Battery expired temperature (+72°F / +22°C)
Storage temperature: -4°F to +158°F /
• Failed device self-test -20°C to +70°C Charged in the external battery charger:
Reporting software over Bluetooth Relative humidity: 5% to 98%, non- • Less than four hours at room
• Report Generator software condensing temperature (+72°F / +22°C)
(DTX, included with device purchase Device IP classification (IEC60529): Battery service life (interval for
for download online) with ability IP43 recommended replacement)
to download, print, save and • Recommendation to replace the
share device reports of each use Operating input voltage: 12-28 V DC
battery every 3 to 4 years or after
(PDF format) Atmospheric pressure: 62-107 kPa 200 uses (of more than 10 minutes
• The Report Generator (DTX) can be -1253 to 13000 ft (-382 to 4000 m) each time)
downloaded on a pc with Windows® • End of Battery service life will be
7, 8.1 or 10 Power specifications indicated by a constant yellow LED
Device data storage: 4GB (estimated to to the far right on the Battery charge
store more than two uses per day over Power source: Proprietary battery indicator
the lifetime of the device, 8 years) alone or with external power supply or
Battery IP classification (IEC60529):
car power cable
IP44
Device physical specifications Power supply input: 100-240VAC,
Battery charge temperature
50/60Hz, 2.3A, Class II
Device dimensions when assembled • +32°F to +104°F / +0°C to +40°C
Power supply output: 24VDC, 4.2A
(HxWxD): 22.0 x 20.5 x 9.4 inches / • (+68ºF to +77ºF / +20ºC to +25ºC
56 x 52 x 24 cm Car power cable: 12-28VDC/0-10A preferred)
Device dimensions while stored in Battery type: Rechargeable Lithium-ion Battery storage temperature
carrying case (HxWxD): 22.8 x 13.0 x Polymer (LiPo) • -4ºF to +104ºF / -20ºC to +40ºC
10.2 inches / 58 x 33 x 26 cm Battery capacity: 3300 mAh (typical), • +105ºF to +158ºF / +41ºC to +70ºC
Battery dimensions (HxWxD): 86 Wh ambient for less than a month
5.1 x 3.5 x 2.2 inches / 13.0 × 8.8 × Battery voltage (nominal): 25.9 V
5.7 cm
Battery run time (nominal patient):
Weight of the device with Battery Battery run time 45 minutes (typical)
(no straps): 17.7 lbs / 8.0 kg Extended run time connecting to
Battery weight: 1.3 lbs / 0.6 kg external power supply

Back plate: Thin and lightweight

back plate (0.6 inches / 15mm and
2.5 lbs / 1.1 kg)
References
1. Rubertsson S, Lindgren E, Smekal D, et al. Mechanical chest compressions and simultaneous defibrillation vs conventional
cardiopulmonary resuscitation in out-of-hospital cardiac arrest. The LINC randomized trial. JAMA. 2013;311(1):53-61.
2. Levy M, Yost D, Walker R, et al. A quality improvement initiative to optimize use of a mechanical chest compression device within a
high-performance CPR approach to out-of-hospital cardiac arrest. Resuscitation. 2015;92:32-37.

The LUCAS 3 device is for use as an adjunct to manual CPR when effective manual CPR is not possible (e.g., transport,
extended CPR, fatigue, insufficient personnel).

Physio-Control is now part of Stryker.

For further information, please contact your Stryker or Physio-Control representative or visit our website at
www.physio-control.com

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