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Mindray ME8

Mindray · ME Series

PortablePoint of CareCardiology

Mindray ME8 portable ultrasound system

The Mindray ME8 is a laptop point-of-care ultrasound system suited to emergency medicine, critical care, anesthesia and ultrasound-guided procedures. It weighs less than 4.0 kg including batteries and has a 15.6-inch LED monitor, a 12.3-inch touch screen and the ZST+ software-based beamformer. Its 510(k) device family includes the MX7, MX8 and ME7; the MX8 has specialized MSK and Cardiovascular configurations.

Released
2021launched by Mindray
Probe ports
13 on the optional cart
Display
15.6-inchLED, 1920 × 1080
Weight
under 4.0 kgincluding batteries

Compatible probes

Linear

  • L9-3s
  • L11-3VNs eSpacial Navi™ enabled
  • L12-3RCs
  • L12-3VNs eSpacial Navi™ enabled
  • L14-6Ns
  • L16-4Hs Intra-operative
  • L20-5s

Convex & microconvex

  • SC5-1Ns
  • C11-3s Microconvex

Phased

  • SP5-1Ns
  • P8-2s
  • P10-4s

Endocavity

  • V11-3Hs

Specialty

  • P7-3Ts Transesophageal
  • P8-3Ts Transesophageal
  • CW2s Non-imaging, cardiac; 2 MHz bandwidth

Specifications

Display
Display
15.6-inch LED monitor, 1920 × 1080, on a 185-degree hinge
Touch screen
12.3-inch, 1920 × 720, multi-gesture, with configurable presets
Secondary display
Shows battery capacity, AC power status and the product model
Physical
Weight
Less than 4.0 kg including batteries; main unit 6.6 lb (3 kg)
Dimensions
(322±5) × (364±5) × (44±3) mm (D × W × H); 1.7 in thick
Probe ports
One on the main unit; up to two with the dual extender; three on the optional cartShow all
Housing
Magnesium-alloy shell
Control panel
Sealed, fluid-resistant and lockable; trackball or trackpad configurations
Cart
Optional, with three probe ports, 320 mm lifting range and 3 storage basketsShow all
Power & battery
Battery
Built-in lithium-ion, 14.4 V, 6600 mAh; 0–100% in under 4 hours when off or in standbyShow all
Battery service life
5 years (lithium-ion battery)
U-Bank external battery
Optional, 2 or 4 batteries: up to 8 hours of continuous scanning; 19 V DCShow all
Power input
100–240 V AC, 50/60 Hz; main unit 2.0–1.0 A; cart 4.4–2.5 A
Connectivity & options
DICOM
DICOM 3.0: worklist, MPPS, storage commitment, storage, print, query/retrieveShow all
Network
Ethernet 10/100/1000BASE-T, single interface; optional WiFi module
Video and data ports
S-Video output, network port, HDMI, USB (disk, barcode reader, printer, footswitch, DVD)Show all
eGateway
Sends images, reports and demographics to electronic patient records
M-Secure
Encryption, DICOM encryption, secure data wipe, anti-virus, OS hardening, access controlShow all
Z-Tracking™
Attaches the serial number of the probe used in an exam to the patient's medical record
Supported peripherals
Printers P95DW-N, UP-X898MD, UP-D25MD; DVD drive GP60NB60; footswitches; barcode readersShow all
Standard configuration
Main unit, adapter, built-in batteries, system software, traveling case, accessoriesShow all
Imaging & software
Imaging modes
B, M, PW, CW, Color and Amplitude Doppler, THI, TDI, 4D, contrast; by configurationShow all
Beamformer
ZONE Sonography® Technology+ (ZST+), software-based
TEE imaging
Transesophageal echocardiography (TEE)
Smart tools
Auto EF, Smart VTI, Smart IVC, Smart B-line, Smart Bladder, Smart FHR, Auto GAShow all
Needle guidance
iNeedle+™ needle visibility; eSpacial Navi™ 4D magnetic needle navigationShow all
HD Scope
Improves detail, contrast and the definition of tissue boundaries
iWorks™
Protocol-based workflow
Optional software
Free Xros M, Free Xros CM, Stress Echo, TDI QA, Tissue Tracking QA; by configuration
Environment
Operating
0 °C to 40 °C; 20% to 85% RH, non-condensing; 700 hPa to 1060 hPa
Storage and transport
-20 °C to 55 °C; 20% to 95% RH, non-condensing; 700 hPa to 1060 hPa
Compliance
FDA 510(k)
K251192 (2025-08-22), K241432 (2024-09-12), K212900 (2021-11-05), K200001 (2020-04-09)Show all
Safety classification
Class I and internally powered; Type-BF applied part; main unit IPX0, adapter IP22Show all

What to check when buying a used Mindray ME8

  1. Check the internal battery's health and history

    Battery work by inadequately trained personnel can cause excessive temperatures, fire or explosion, and a unit left in standby through storage or transport drains its batteries and damages them permanently.

    How: Have a technician run the battery health status test, and ask who last installed the battery, since only Mindray technical staff or Mindray-trained engineers may install or remove it.

  2. Inspect each probe head and cable

    A probe with a damaged or scratched surface or exposed wiring must not be used, and a defective transducer can cause an electric shock.

    How: Look for cracks or swelling on the head and for aging, blistering, deterioration or erosion along the cable, and ask whether any probe was knocked or dropped.

  3. Have a biomed run electrical safety tests

    Electrical and mechanical performance can degrade with long use, through leakage, distortion and abrasion, so an older unit needs measuring.

    How: Ask for a safety-analyzer report with protective earth resistance and earth leakage results, and check that every label from Mindray or the previous facility is present and legible.

  4. Reject aftermarket probes Mindray does not specify

    Probes other than those Mindray specifies can damage the system and, in the worst case, cause a fire.

    How: Confirm every probe offered with the unit is a Mindray model specified for it.

Common questions about the Mindray ME8

Is the Mindray ME8 FDA-cleared?

Yes. The ME8 is FDA-cleared through 510(k) as a Class II device under 21 CFR 892.1550, product codes IYN, IYO and ITX. Its most recent clearance is K251192, decided on August 22, 2025; earlier clearances naming it are K241432 (September 12, 2024), K212900 (November 5, 2021) and K200001 (April 9, 2020), the earliest on record. Each one clears a family of Mindray systems that includes the ME8.

What exams is the Mindray ME8 cleared for?

The clearance covers adults, pregnant women, pediatric patients and neonates. Its cleared exams are ophthalmic, fetal, abdominal, pediatric, small organ (breast, thyroid, testes), neonatal and adult cephalic, trans-rectal, trans-vaginal, musculoskeletal (conventional and superficial), thoracic/pleural, adult and pediatric cardiac, peripheral vessel and urology, plus intra-operative (abdominal, thoracic, vascular), laparoscopic and trans-esophageal (cardiac) use.

The intra-operative and trans-esophageal applications came with K212900 in 2021.

How does the Mindray ME8 differ from the MX8?

The ME8 is marketed for point-of-care ultrasound, while the MX8 has specialized MSK and Cardiovascular configurations. Both sit in one 510(k) device family with the MX7, MX7T, Vaus7, Zeus, ME7, Anesus ME7, Anesus ME7T, MX7P, MX7W, MX8T, Vaus8, Nuda, Aquila and Malody, and one operator's manual covers all of those model names.

What warranty comes with a new Mindray ME8?

A new ME8 bought directly from Mindray North America carries a standard five-year warranty covering parts, including the cart, scan module and standard transducers; warranties through Mindray's agents can vary. The ME8 is also a covered system under Mindray's portable Ultrasound Support Plan, a mail-in warranty for new systems bought directly through Mindray.

Support includes technical telephone help and mail-in service, with a loaner while the system is under warranty.

Are software updates free on the Mindray ME8?

For a system under warranty, yes. The standard warranty includes software updates, and Mindray's Living Technology updates come at no charge for systems under warranty, installation not included; new application packages and hardware upgrades are optional purchases.

Owners cannot patch the system themselves: Mindray evaluates every update or patch, and only its service engineers, or engineers it designates, notify owners of software and hardware version updates.