Instructions for Use

Technical specifications

Following are the technical information regarding ECG module, its measurement and patient cable provided within the package.

3.1 MESI ECG MODULE

3.1.1 DIMENSIONS

Width: 40 mm

Depth: 48 mm

Height: 135 mm

Weight: 220 g

3.1.2 POWER & BATTERY

Power & Battery
Column AColumn B
AC/DC adaptorFW8030M/05
Input100-240 V AC / 50-60 Hz / 600-300 mA
Output5 V DC / 5.0 A
Battery typeRechargeable Lithium-Polymer battery
Capacity1240 mAh
Examinations per battery charge> 100
Charging timeCharge time for depleted battery: approximately 2 hours (minimum charge time for 1 automatic mode ECG: 10 minutes)

3.1.3 CLASSIFICATION

Classification
Column AColumn B
Protection against electric shock Class II equipment
Medical device classificationClass IIa
Applied partsType CF defibrillation protected
IEC 60601-1 (2006)General requirements for basic safety and essential performance
IEC 60601-1-2 (2015)General requirements for basic safety and essential performance – Collateral standard: Electromagnetic compatibility – Requirements and tests
IEC 60601-2-25Particular requirements for the basic safety and essential performance of electrocardiographs

3.1.4 OPERATING CONDITIONS

OPERATING CONDITIONS
Column AColumn B
Temperature, operating10° to 40°C
Relative humidity25 to 85% (no condensation)
Pressure during operation700 to 1060 hPa
Ingress protectionIP44

3.1.5 TRANSPORT & STORAGE CONDITIONS

TRANSPORT & STORAGE CONDITIONS
Column AColumn B
Temperature-15° to 50°C (< 1 month) / -15° to 40°C (< 3 months) / -15° to 25°C (< 12 months)
Relative humidity25 to 85 % (no condensation)
Pressure during operation700 to 1060 hPa
Ingress protectionIP44

3.1.6 MEASUREMENT SPECIFICATIONS

MEASUREMENT SPECIFICATIONS
Column AColumn B
Lead-fail indicationDisconected lead detection
Pacemaker detection> ± 2 mv / 0.1 ms
Patient input circuitryFully floating and isolated, defibrillation protected (only with original MESI or approved patient cable)
Channel crosstalk< 2% of applied signal
Input impedance1000 MΩ
Noise level< 30 μVpp
Frequency responseNominal input amplitude response 1 mVpp 1,5 mVpp Relative output amplitude response +/- 10 % 0 % / - 10 %
Impulse response< 0.30 mV/s
Linear & Dynamic range< 5% of output signal change

3.1.7 ACCURACY

Accuracy
Column AColumn B
CMRR> 110 dB
Sampling rate32 K samples/second/channel
Resolution2.5 uV / 19 bit
ECG analysis frequency1000 samples/second
Pacemaker detection≥ ± 2 mv / ≥ ± 0.1 ms
SamplingUniform sampling - 1 kHz Simoultaneous sampling - Skew << 10 μs
Amplitude quantisation143 nV

3.1.8 PROCESSING

PROCESSING
Column AColumn B
InterpretationUniversity of Glasgow Analysis Software
Patient dataname, BP, BPM, time and amplitude, recording duration
Low-pass filter150 Hz, 250 Hz
High-pass (baseline) filter0.05 Hz, 0.2 Hz, 0.5 Hz
Myogram (muscle tremor) filter25 Hz (40 dB/dec) or 35 Hz (20 dB/ dec)
Mains filterDistortion-free suppression of superimposed 50 or 60 Hz sinusoidal interferences by means of an adaptive digital filter
Graph display6:6+1, 6:6, 3x3 main, 3:3 aux, 6 main, 6 aux, 3:4, 12, custom
Sensitivity5 mm/mV, 10 mm/mV, 20 mm/mV

3.2 PATIENT CABLE

The basic package includes a patient cable for 12-lead ECG with snap connectors on lead cables. Leads are paired into three groups based on length and body application.

RA, LA, RL, LL leads - Group length: 110 cm

C1-6 leads - Group length: 75 cm

MESI mTABLET ECG - Patient cable

3.3. CALIBRATION AND SAFETY CHECK

Calibration of the MESI ECG UNIT is not required. To ensure safety and optimal performance, the device should be inspected by a qualified service engineer at least once every 12 months. This inspection should include safety checks for mechanical or functional damage to the device and its accessories and verification of performance in accordance with the instructions for use.

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