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Philips CX50

Philips · CX series

PortableCardiologyVascular

Philips CX50 portable ultrasound system

The Philips CX50 is a laptop-style portable ultrasound system carrying technologies from the premium Philips iE33 and iU22 systems. Philips configured it for general imaging, critical care, vascular and regional anesthesia, and the CX50 xMATRIX for diagnostic, interventional, surgical and pediatric echocardiography. Its predecessor is the HD11XE; the cart-based Sparq shares its technology.

Released
2008launched by Philips
Probe ports
1 imaging3 with the multiport adaptor
Display
39.1 cmhigh-resolution LCD
Weight
6.17 kgsystem only

Compatible probes

Linear

  • L12-3
  • L12-5/50
  • L15-7io Compact linear; intraoperative
  • L10-4lap Laparoscopic

Convex & microconvex

  • C5-1 PureWave
  • C8-5
  • C9-3io Intraoperative

Phased

  • S4-2
  • S5-1 PureWave
  • S8-3
  • S12-4

Endocavity

  • C10-3v PureWave; intracavity

Specialty

  • X7-2t PureWave TEE; Live 3D on CX50 xMATRIX
  • X8-2t PureWave TEE; Live 3D on CX50 xMATRIX
  • S7-3t Pediatric and adult 2D TEE
  • ViewFlex Xtra Third-party ICE catheter; CX50 xMATRIX
  • D2cwc Non-imaging CW probe
  • D5cwc Non-imaging static Doppler

Specifications

Display
Display
High-resolution LCD, single monitor, 39.1 cm (15.4-inch)
Physical
Weight
6.17 kg, system only; 7.3 kg as specified in 2014
Weight with cart
52 kg, system and cart
Dimensions
41.3 cm wide, 35.6 cm deep, 7.6 cm high (8.6 cm high as specified in 2014)
Probe ports
1 imaging and 1 pencil-probe port; up to 3 transducers via the multiport adaptorShow all
Controls
Keyboard with Patient and Transducer keys, trackball, Quick Keys, tri-state lightingShow all
Carts and carrying
Height-adjustable cart that swivels and locks; travel case; carry handleShow all
Control panel height adjustment
82.8–107.9 cm
Packaging weight
46.2 kg total: wood 25.5 kg, cardboard/paper 18.4 kg, plastic 2.1 kg, ferro metal 0.2 kg
Power & battery
Battery
Internal lithium-ion polymer battery with quick-charge; runs on AC or batteryShow all
Power input
100–240 V AC, 50/60 Hz, 2.65 A, with the AC adapter
Power consumption
200 W on; 80 W ready to scan or standby; 0 W off
Energy usage
554.8 kWh per year in an average-use scenario
Connectivity & options
Network
Ethernet 10/100/1000BaseT and 802.11 a/b/g/n wireless (CX50 5.5)
DICOM
DICOM to PACS, wired or wireless; storage, worklist, MPPS, print and structured reportsShow all
Secure DICOM
Optional TLS encryption with certificate management (CX50 5.0.X)
Security
Firewall, OS hardening, malware protection, access controls, patient data encryptionShow all
Export
CD/DVD and USB export with an integrated DICOM viewerShow all
Image storage
Local repository; off-line storage to network, DVR, DVD or USB in JPEG, AVI and DICOM
Hard drive
160 GB, as specified in 2014
Video output
DVI-I digital output for cath and EP labs with VGA, DVI-I or HDMI inputs (CX50 xMATRIX)
Cath lab integration (CX50 xMATRIX)
Xper Module tableside control, EchoNavigator 2.0, automatic patient data exchangeShow all
Digital Navigation Link (DNL)
Real-time image link
Remote services
ISSL link: proactive monitoring, remote desktop, support request button (optional)Show all
Service tools
On-cart (non-phantom) transducer test; per-transducer usage reports by exam type
Remote Reporting
Qview remote reporting, available only with Qpath (CX50 POC)
Purchasable imaging options
LVO Contrast, Physio, Stress Echo Protocol; availability varies by transducer and region
Imaging & software
Imaging modes
B, M-mode, Anatomical M-mode, PW, CW, Color Doppler, Tissue Doppler, CPA, harmonicsShow all
Revision and software
Cleared releases 1.0, 2.0, 3.0 and 4.0; software labels R1.0.x through v5.5Show all
Beamformer
Digital broadband beamformer
Channels
128-channel system; 128 transmit and 256 receive channels, 128/128 beamformer
Digitally processed channels
Up to 504,576, as specified in 2014
Dynamic range
170 dB full-time system dynamic range
Image processing
SonoCT compound imaging (up to nine lines of sight), XRES, Advanced XRES, PureWaveShow all
Optimization
iSCAN one-button 2D and Doppler (3D on xMATRIX), AutoSCAN, Smart TGC, HD ZoomShow all
Presets
Tissue-specific presets; FAST and Lung presets
Active native data
Scanning parameters adjustable on stored images, clips, 2D and Doppler data
Doppler tools
High Q automatic Doppler analysis; Intelligent Doppler holds the selected Doppler angle
Exam protocols
SmartExam protocols with on-screen guidance, automatic annotation and report building
Review
Cineloop review of buffered images
CX50 POC tools
Live compare, side-by-side M-mode for lung imaging, Hide patient ID, Temporary IDShow all
Needle visualization
On the L12-5 and L12-3 transducers
Gain Save
Recalls image settings for each view in stress echo
3D
Freehand 3D volume acquisition
Live 3D (CX50 xMATRIX)
Live 3D, Live 3D Color, Live 3D Zoom with Preview, Full Volume, Live xPlane, Live 3D TEEShow all
3D tools (CX50 xMATRIX)
3D Depth Markers (up to three per volume), 3D Orientation Marker, Auto Crop, SwivelShow all
Intracardiac echo
2D ICE with the ViewFlex Xtra catheter (CX50 xMATRIX)
QLAB
Quantification software with Q-Apps
QLAB cardiac
CMQ, aCMQ A.I. (2D GLS with Auto-ROI EF), MVN A.I., MVQ, Cardiac 3DQ and 3DQA, SQ, TMQShow all
QLAB general imaging
IMT, GI 3DQ, MVI, ROI, iSlice (4, 9, 16 or 25 slices)Show all
Environment
Heat output
700–1100 BTU/hour, fully loaded, as specified in 2014
Compliance
FDA 510(k)
K201012 (2020-05-01), K162329 (2016-09-14), K123754, K111513, K091804, K081802Show all
Environmental compliance
RoHS 2 (EU Directive 2015/863) and REACH

What to check when buying a used Philips CX50

  1. Inspect the power cord and socket for damage

    One CX50 power cord, punctured and stripped of its insulation, exposed a live wire that shocked a user lifting the system, and another, pulled too hard, tore its wires out and left the power socket charred.

    How: Check the cord end to end for punctures or stripped insulation, and the power socket on the system for charring or loose wires.

  2. Reject a swollen or burned battery

    A CX50 battery has been found swollen with its case split, and a burned battery and power supply were traced to a worn-out battery.

    How: Take the battery out and look for swelling, a split case or burn marks, and check the system's plastic housing for a seam parting along its weld line.

  3. Inspect every transducer, cable and connector

    A transducer or cable showing cracks, splits, fluid leaks, sharp edges or projections must be taken out of use.

    How: Examine every part of each transducer, its cable and its connector, and set aside any probe showing that damage.

  4. Check TEE probes against recall Z-1841-2020

    Some S7-3t and S8-3t TEE transducers left manufacturing misprogrammed, so an affected probe on a CX50 cannot report its true tip temperature and does not start auto-cool.

    How: A CX50 cannot detect an affected probe, so get proof that Philips completed the recall correction on any S7-3t or S8-3t offered with the unit.

Common questions about the Philips CX50

What configurations does the Philips CX50 come in?

Philips offered the CX50 in four clinical configurations: General imaging, Critical care, Vascular and Regional anesthesia. The CX50 POC is the configuration for critical care and emergency medicine, and for regional anesthesia and pain medicine.

The CX50 xMATRIX is the configuration for diagnostic, interventional, surgical and pediatric echocardiography, and it adds Live 3D TEE on the X7-2t transducer. It launched in 2012, and 2D intracardiac echo was added in May 2013.

Is the Philips CX50 discontinued?

Yes, in its four clinical configurations: Philips no longer offers the General imaging, Critical care, Vascular or Regional anesthesia CX50. Philips's Italian catalog still carries the CX50 xMATRIX.

Is the Philips CX50 FDA-cleared?

Yes. The CX50 Diagnostic Ultrasound System is a class II device cleared through FDA 510(k), under product codes IYN, IYO and ITX. Its first release was cleared under K081802 on July 11, 2008.

Later clearances are K091804 for CX50 2.0 (July 17, 2009), K111513 adding pediatric cardiac and neonatal cephalic indications (June 24, 2011), K123754 for CX50 3.0 with intracardiac echo, intraoperative and laparoscopic indications (December 21, 2012), K162329 for CX50 4.0 (September 14, 2016) and K201012, which expanded its labeling for lung and cardiac imaging of COVID-19 patients (May 1, 2020).

What is the difference between the Philips CX50 and the Sparq?

Both use the same technology. The CX50 is built into a portable, laptop-style chassis with an optional cart, while the Sparq is a cart-based mobile system with a capacitive touch interface and an articulating monitor arm. The Sparq has no 3D matrix array transducers.