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Patient Monitor Model PM9000 Feas Electrónica
MULTIPARAMETER PATIENT MONITOR Model: PM9000
GENERAL CHARACTERISTICS
Features:
Menu, messages and instructions in English or Spanish.
Single sweep speeds for circulatory (25mm/s y 50mm/s) and respiratory system (6,25 mm/s, 12,5 mm/s, 25 mm/s y 50 mm/s).
Visual and audible QRS indicator proceeding from ECG or Oxymeter.
When QRS proceeds from the Oxymeter, the sound changes its tone as SpO2 modifies.
Physiological and technical alarms.
Three alarm priority levels: low, medium and high priority.
Upper and lower limits adjustable by the user.
Visual and audible alarm indicators, on screen and on top of the equipment.
Hotkey to pause visual or audible alarms for 2 minutes.
Visual or audible alarms Turn Off function.
User friendly menu by using the trim knob and hotkeys.
Networking Connection for Centralized Monitoring.
Screen menu: - Normal.
- 7 leads of ECG.
- Tabular trends or graphical trends.
- Big numbers
- OxyCRG
BASIC CHANNELS
Electrocardiogram (ECG)
Heart rate: Adult 15 to 300 1/min. Pediatric 15 a 350 1/min
Gain selection: 0.25, 0.5, 1 and 2 cm/mV, individual or for both channels.
Visual and audible QRS indication.
Automatic selection of 3 or 5 leads patient cable.
3 leads with 3 leads patient cable. Lead selection: DI, DII or DIII.
7 leads with 5 leads patient cable. Lead selection: DI, DII, DIII, aVR, aVL, aVF and C.
50Hz or 60Hz Notch filter and Diagnostic, Monitoring or Surgery filter.
Heart rate alarms: Lower and upper (medium priority).
Lower and upper extreme (high priority) and off.
Lead off detection.
Pacemaker pulse indication.
Pacemaker pulse rejection in counting the heart rate:
Pulse rejected characteristic: -Amplitude: from ±2 mV to ±700 mV.
-Pulse width: from 0.1 ms to 2.0 ms.
Analysis and classification of arrhythmias
Detected and classified the follow arrhythmias: PVC, PAC, PNC, Bigeminy, Trigeminy,
Couple, Run, Tachycardia, Bradycardia, VT, VF and Asystole.
Measurement of the S-T segment: both the isoelectric point and the ST point areuser adjustable.
Range: ±2.00 mV. PVCs per minute measurement.

Respiratory waveform (RESP)
Impedancemetry Method.
Measurement selection: Transabdominal (II-F) o Transthoracic (I-L).
Respiratory rate: 5 to 170 1/min.
Apnea Alarm.
Respiratory rate alarm, minimum and maximum: 5 to 170 1/min.

Oxygen saturation (SpO2)
Plethysmographic waveform, Display of percentual oxygen saturation.
Measurement signal low perfusion and motion.
SpO2:
Range: 0% to 100%.
Adult precision: 2% from 70% to 100%.
Neonate precision: 3% from 70% to 100%.
Motion precision: 3% from 70% to 100%.
Resolution: 1%.
Alarm: 0% to 100% and off.
Initial alarm: 85%.
Pulse rate:
Range: 20 to 250 1/min.
Adult precision: ±3 1/min.
Neonate precision: ±3 1/min.
Motion precision: ±5 1/min.
Resolution: 1 1/min.
Alarm: 20 to 250 1/min and off.

Two channels of invasive blood pressure (IBP)
Simultaneous measurement of Systolic, Diastolic and Mean pressure.
Range: -30 to 300 mmHg.
Mode selection for Pressure Ranges: Automatic or Manual.
Mean Pressure alarm: minimum and maximum limits from -30 to 300 mmHg and off.
Technical alarm due to transducer failure and disconnected catheter.
Label: ART, AoP, LVP, PAP, CVP, WDG, RAP, RVP, ICP, IAP and IEP.
Units in mmHg.
CVP, ICP, IAP and IEP can measure in mmHg or cmH20.

Two temperature channels
Compatible with Thermistor Series YSI 400.
Measurement of body temperature (25°C a 50°C) or injectate temperature during measurement of Cardiac Output, from (-10ºC to 25ºC).
Resolution: 0.1ºC. Accuracy: ±0.2ºC.
Temperature Alarm, minimum and maximum:(25ºC to 50ºC) and off.

Cardiac output (CO)
Input of patient parameters: Weight, height.
Selection of: Injectate volume: 3, 5 and 10 ml.
Catheter Constant K or Computing Constant (CC).
Measurement of temperature in blood and injected.
Calculation of: Body surface.
CO: Volume in liters/min.
SV: Systolic volume.
CI: Cardiac index.
SI: Systolic index.
Waveform graph for blood temperature as a function of time.
Manual or automatic start of the measurement, at perform the injection.
Stores 8 measurements.
Blood temperature: Range 15°C to 45°C, resolution 0.01°C and accuracy ±0.3°C.
Injected temperature: Range -10°C to 25°C, resolution 0.1°C and accuracy ±0.4°C.

Non-invasive blood pressure (NIBP)
Oscillometric method
Use: ADULT/PEDIATRIC or NEONATE.
Measurement mode: AUTOMATIC or MANUAL.
Unit in mmHg.
Resolution:
Pressure: 1 mmHg.
Pulse rate: 1 1/min.
Transductor accuracy: ±3 mmHg or ±2%, whichever is greater.
Ranges:
ADULT/PEDIATRIC
Pressure: Systolic: 25 to 265 mmHg.
Diastolic: 12 to 220 mmHg.
Mean: 18 to 245 mmHg.
Pulse rate: 40 to 240 1/min.

NEONATE
Pressure: Systolic: 25 to 135 mmHg.
Diastolic: 12 to 110 mmHg.
Mean: 18 to 120 mmHg.
Pulse rate: 40 to 240 1/min.

Alarm limits of: Systolic pressure from 20 to 255 mmHg and off.
Diastolic pressure from 5 to 220 mmHg and off.
Display of the last 1440 measurements (48 hours, every 2 minutes).
Print-out of the measurements in table form.
Manual or automatic start of the measurement at programmable intervals of 2, 3, 4, 5, 10, 15, 30, 60 and 90 minutes.
Protections: Double protection from over-pressure.
Over-pressure of 300 mmHg + 20 mmHg for the Adult mode.
Over-pressure of 150 mmHg + 15 mmHg for the Neonate mode.
Protection for exceeding the time of measurement.

OPTIONALS
FiO2
Fraction of inspired Oxygen: from 0% to 100%.
Galvanic cell measurement principle.
Alarms minimum and maximum: 18% to 100% and off.

Recorder
Direct access key for record command.
High resolution thermal array printer.
Recorder speed: 25 mm/s.
Recorded in real time up to 2 selectable waveforms between ECG, RESP, IBP,
SpO2 and CO2 waveform.
Prints the header with date and time.
Print values of Sweep Speed, Lead, Gain, Respiratory Rate, Heart Rate,
Systolic, Diastolic and Mean Pressure, SpO2 and Pulse Rate, EtCO2, FiCO2
and Respiratory Rate (CO2), according recorded waveform.

Capnography

Option 1: Sidestream
Measurement of EtCO2, FiCO2 and Respiratory Rate.
Range: CO2, from 0 to 100 mmHg (0% to 13%).
Respiratory Rate: 4 to 150 1/min.
Accuracy: from 0 mmHg to 38 mmHg: ±2.0 mmHg
from 39 mmHg to 70 mmHg: ±5 mmHg
from 71 mmHg to 100 mmHg: ±8 mmHg
Resolution: CO2, 1mmHg.
Respiratory Rate, 1 1/min.
Alarm: FiCO2, EtCO2 minimum and maximum, 0 to 100mmHg and off.
Respiratory Rate minimum and maximum, 0 to 150 1/min and off.
Calibration: Two zero points -room air and gains (5% or 10%)-.

Option 2: Sidestream with anesthetic gases measurement
Measurement of EtCO2, FiCO2 and Respiratory Rate.
Range: CO2, from 0 to 100 mmHg (0% to 13%).
Respiratory Rate, 4 to 150 1/min.
Accuracy: CO2, ±3%ABS.
Resolution: CO2, 1 mmHg.
Respiratory Rate, 1 1/min.
Alarm: FiCO2, EtCO2 minimum and maximum, 0 to 100 mmHg and off.
Respiratory Rate minimum and maximum, 0 to 150 1/min and off.
Measurement of expired and inspired O2: from 0% to 100%, Resolution: 1%.
Measurement of N2O: from 0% to 100%.
Automatic detection and measurement of up two anesthetic gases: Halothane, Enflurane,
Isoflurane, Sevoflurane and Desflurane.
- Range: 0% to 30%.
- Accuracy: ±8%REL.
- Resolution: 0.1%.
Flowrate: 70 to 120 ml/min for neonatal patients.
120 to 250 ml/min for adult patients.

Option 3: Mainstream
Measurement of EtCO2, FiCO2 and Respiratory Rate.
Range: CO2, from 0 to 100 mmHg (0% to 13%).
Respiratory Rate, 4 to 170 1/min.
Accuracy: ±2 mmHg from 0 to 40 mmHg.
±5% of reading from 41 to 70 mmHg.
Resolution: 1 mmHg.
Calibration: only zero (room air).
Compensation for temperature and atmospheric pressure, O2 y N2O.
Warm-up time <15s, to start measuring, within 2 minutes to obtain values consistent with the specifications.
Waveform response time: less than 60ms.

Touchscreen

ACCESSORIES
Included:
3 or 5 leads patient cable.
Disposable electrodes.
SpO2 sensor.
Pressure Transducer Adaptor (1 units).
Pressure transducer (1 units).
Temperature sensor.
Power cord.
User manual.

TECHNICAL SPECIFICATIONS
15” LCD Color Monitor. Resolution: 1024 x 768. Greater angle of view.
Dimensions: Height: 345mm; Width: 335mm; Depth: 205mm.Weight: 6 Kg.
Power Supply: 90V~ to 240V~ (with automatic voltage selection) 50Hz or 60Hz.
Power Consumption: 65VA.
Internal Battery: 14.4V / 8.8Ah Li-ion battery. Autonomy: 3.5 hours.
Battery state indication (empty, full, on charge) on screen.
Quality Standard: ISO 13485, Disp. A.N.M.A.T. 3266/2013: B.P.F. and
Disp. A.N.M.A.T. 2319/02, certified.
Safety Standard: UNE-EN60601-1. (Eq. IRAM 4220-1 and IEC 601-1) Electrical-
shock protection: Class I - CF, UNE-EN60601-1-2 (EMC), certified.


The images shown are for illustrative purposes only and may differ from the actual product. Specifications are subject to change without notice.
Defibrillator Monitor 3850B Biphasic Feas Electrónica
Feas Electronica Model 3850B Biphasic is an external defibrillator monitor with a rectilinear biphasic waveform of up to 200J, selectable in steps, which allows defibrillation in asynchronous or synchronized mode with the R wave of the patient's ECG for the application of synchronized cardioversion.
It allows the monitoring and surveillance of ECG, with heart rate measurement, through the paddles, or cable to patient with 3 lead or 5 lead.

In addition, optionally, you can monitor pulse oximetry, graphing the plethysmographic curve on the screen and a pulse width indicator bar, indicating the SpO2 and pulse rate values. Both ECG and SpO2 monitoring allow the setting of alarms that allow monitoring of heart rate, SpO2 value and pulse rate.

It is of the portable type, powered by an internal rechargeable battery, a 90 Vac - 240 Vac, 50 Hz or 60 Hz mains supply or an external 12 Vdc source.
Optionally, it has a transcutaneous pacemaker that allows temporary electrical stimulation to the patient in a non-invasive way, in fixed mode (asynchronous) or on demand (synchronous), using electrodes.

Optionally, it can also have a thermal recorder for real-time recording of up to two curves, an ECG lead, and optionally the plethysmographic curve, manually when the operator decides or automatically during charging.

FEATURES

MONITOR
• Electrocardiogram monitor with LCD screen.
• Electrocardiogram signal acquired through 3 or 5 leads patient cable or through paddles.
• Leads selection:
- With 3 lead cable: DI, DII, DIII and PAL.
- With 5 lead cable: DI, DII, DIII, aVR, aVF, aVL, precordial and PAL.
• ECG Gain: 1/6, 1/4, 1/2, 1 and 2 cm / mV.
• ECG waveform cascade.
• Digital indication of heart rate.
• Low battery indicator.
• Luminous Indicator of battery charging.
• Alarms silence key.
• Alarms for Heart Rate from 20 ppm to 250ppm.

DEFIBRILLATOR
• Biphasic waveform.
• Defibrillator use in three steps:
1- Turn on and select energy.
2- Load.
3- Trigger energy discharge by means of push buttons on paddles or from the keyboard.
• Selector switch for charge selection by steps: 2, 3, 5, 7, 10, 20, 30, 50, 70, 100, 150, 200 Joules.
• Visual and audible indication of charging process completed.
• Stored energy indication on display.
• Energy discharge through paddles by pushing, simultaneously, both pushbuttons on paddles.
• Charge is cancelled internally: When the key DISARM is pressed or when 60 seconds have elapsed since charge process was completed or when selector switch is turned to MONITOR or OFF.
In these cases the energy is discharged internally without reaching the paddles.
• Direct or synchronized discharge.
• Visual and audible indication of synchronized mode.
• Discharge capacity: 150 discharges at maximum energy, with fully charged internal battery.
• Charging time to 200 J, less than 6 seconds.
• The equipment has a power test delivered.

RECORDER (OPTIONAL)
• Direct access key for record command.
• Automatic registration when the power charge process starts up to 20 seconds after pressing the Shock key.
• High resolution thermal array printer.
• Registration speed: 25 mm / s.
• Prints: date and time, energy in joules, Elctrocardiogram waveform, Gain, Heart Rate, Lead, Sweep Speed, Plethysmographics waveform, SPO2, Pulse Rate, Mode, Pacemaker Rate, Pacemaker Current.
• Paper: Width: 50 mm and Diameter Max: 45 mm.
Accessory Included:
50 millimeter roll of paper.

OXYGEN SATURATION (SpO2) (OPTIONAL)
SPO2 measurement:
• Range: 0 to 100%.
• Precision:
Adult ± 2% from 70% and 100%.
Neonatal: ± 3% from 70% and 100%.
In movement: ± 3% from 70% and 100%.
• Resolution: 1%.
• Percentual oxygen saturation alarm:
Upper limit: 1 to100.
Lower limit: 0 to 99.
• Pulse Rate and alarms measurement from 30[1/min] to 250 [1/min] ± 3[1/min] and ± 5 [1/min] with movement.
• Resolution: 1 [1/min].
Accessories included:
Oximetry Sensor Extender
Choice of adult or pediatric, clip-on or disposable oximetry sensor.

TRANSCUTANEOUS PACEMAKER (OPTIONAL)
• External stimulation through electrodes.
• Frequency: 40 ppm to 180 ppm (selectable in steps of 5 ppm).
• Current: 10 mA to 200 mA (selectable in steps of 5 mA).
• Mode: Selectable, on demand or fixed.
• Pulse width: 20 ms ± 5%.
Accessories included:
Elastic belt for external Pacemaker electrode.
Pacemaker lead cable.
Pair of gray electrodes.

TECHNICAL SPECIFICATIONS
• Power input: 90Vac ~ to 240Vac - 50Hz/60Hz or 12 Vcc.
• Rechargeable internal battery, NiMH - 12V, 3500 mAh.
• Power requirement: 180 W (7W during standby).
• Size: 295mm (width) x 200mm (height) x 345mm (length).
• Weight: 6 kg (including external paddles, battery and recorder).

CERTIFICATIONS
• Quality standards:
- CE Marking, Dir. 93/42 / EEC (certificate).
- ISO13485 (certificate).
- Disp. A.N.M.A.T. 3266/2013: B.P.F.
- Disp. A.N.M.A.T. 2319/02.
• Safety rules:
- EN 60601-1 (Eq IRAM 4220-1 and IEC 601-1).
- EN 60601-1-2 (EMC).
- EN 60601-1-6.
- EN 60601-1-8.
- EN 60601-2-4.
- EN 60601-2-27.
- EN 60601-2-49.
- ISO 80601-2-61.
Authorized by the A.N.M.A.T. PM-1125-15.

INCLUDED ACCESSORIES
External paddles for adults and pediatric with coil cable.
Power cable for external +12 power supply.
AC Power cord.
3 or 5 wire cable for patient for ECG.
Disposable electrodes.
User's manual.

The image is illustrative.

The images shown are for illustrative purposes only and may differ from the actual product. Specifications are subject to change without notice.
Patient Monitor, Multiparameter, LCD, Feas Electrónica
Feas Electrónica MULTIPAR LCD Patient Monitor is designed for monitoring the vital signs of patients in Intensive Therapies, Coronary Units, Operating Rooms, Emergency Rooms, and in a wide variety of clinical-hospital environments, where several vital signs need to be monitored of a patient simultaneously.

GENERAL CHARACTERISTICS
FUNCTIONS:
• Menu, messages and instructions in English.
• Single sweep speeds for circulatory and respiratory system: 12.5, 25 and 50 mm/s.
• Visual and audible QRS indicator proceeding from ECG or Oxymeter.
• When QRS proceeds from the Oxymeter, the sound changes its tone as SpO2 modifies.
• Three alarm levels: physiologicals, technicals and generals.
• Upper and lower limits adjustable by the user.
• Visual and audible alarm indicators, on screen and on top of the equipment.
• Hotkey to activate the silent alarms for 2 minutes.
• Alarms Turn Off.
• User friendly menu by using the selector knob and hotkeys.
• Waveform print-out on standard printer.
• Analog outputs for ECG, RESP, IBP and a synchronization pulse.
• Networking Connection for Centralized Monitoring.
• WAIT Mode: stops monitoring, which allows changing to another patient without activating the alarms.
• Screen menu: normal, 7 leads of ECG, Tabular trends or graphical trends, frozen and measuring of calipers, large numbers.

BASIC CHANNELS
ELECTROCARDIOGRAM
• Heart rate: 20 to 300 1/min.
• Gain selection: 1/4, 1/2, 1, 2 and 4 cm/mV, individual or for both channels.
Visual and audible QRS indication.
Automatic selection of 3 or 5 leads patient cable.
• 3 leads with 3 wire patient cable. Lead selection: DI, DII or DIII.
12 leads with 5 wire patient cable. Lead selection: DI, DII, DIII, aVR, aVL, aVF and C1, C2, C3, C4, C5 or C6.
50Hz or 60Hz Notch filter and Diagnostic, Monitoring or Surgery filter.
• Heart rate alarms, minimum and maximum: 20 to 300 1/min and off.
Lead off detection.
Pacemaker pulse detection.
• Pacemaker pulse rejection in counting the heart rate:
•Pulse rejected characteristic:
- Amplitude: from ±2 mV to ±700 mV
- pulse width: from 0.1 ms to 2.0 ms.

ANALYSIS AND CLASSIFICATION OF ARRHYTHMIAS
• Detects and classifies the following arrhythmias: PVC, PAC, PNC, Bigeminy, Trigeminy, Couple, Run, Tachycardia, Bradycardia, VT, VF and Asystole.
• Store up to 32 events and allows review and printing.
• Measurement of the S-T segment: both the isoelectric point and the ST point are user adjustable (J-point +60 ms or +80 ms, or any other value in ms, from 1 to 120 ms).
• Range: ±2.00 mV.

OXYGEN SATURATION
Plethysmographic waveform, display of oxygen saturation (SpO2).
Measurement signal low perfusion and motion.
• SpO2:
- Range: 35% to 100%
- Precision:
±2% from 80% to 100%.
±3% from 70% to 79%.
- Resolution: 1%.
- Alarm: 0% to 100% and off.
- Initial alarm: 85%.
• Pulse rate:
- Range: 25 to 250 1/min.
- Precision: ±2 1/min.
- Resolution: 1 1/min.
- Alarm: 20 to 300 1/min and off.
Waveform gain adjustment x1/2, x1 and x2.

Accessories included:
Finger pulse oximeter sensor.

RESPIRATORY WAVEFORM
Impedanciometric method.
• Measurement selection: Transabdominal or Transtoraxic.
• Respiratory rate: 5 to 170 1/min.
Apnea Alarm.
• Respiratory rate alarm, minimum and maximum: 5 to 170 1/min and off.

NON-INVASIVE BLOOD PRESSURE (NIBP)
Oscilometric method.
• Use: ADULT or NEONATE.
• Measurement mode: AUTOMATIC or MANUAL.
• Measure unit: mmHg.
• Resolution:
- Pressure: 1 mmHg.
- Pulse rate: 1 1/min.
• Transductor accuracy: ±3 mmHg.
• Ranges:
- PEDIATRIC/ADULT
Systolic pressure: 25 to 265 mmHg.
Diastolic pressure: 12 to 220 mmHg.
Mean pressure: 18 to 245 mmHg.
Pulse rate: 40 to 240 1/min.
- NEONATE
Systolic pressure: 25 to 135 mmHg.
Diastolic pressure: 12 to 110 mmHg.
Mean pressure: 18 to 120 mmHg.
Pulse rate: 40 to 240 1/min.
• Alarm limits of:
- Systolic pressure from 20 to 255 mmHg and off.
- Diastolic pressure from 5 to 220 mmHg and off.
Display of the last 1440 measurements (48 hours, every 2 minutes).
Print-out of the measurements in table form.
Manual or automatic start of the measurement at programmable intervals of 2, 3, 4, 5, 10, 15, 30, 60 and 90 minutes.
• Protections:Double protection from over-pressure.
- Over-pressure of 300 mmHg + 20 mmHg for the Adult mode.
- Over-pressure of 150 mmHg + 15 mmHg for the Neonate mode.
- Protection for exceeding time of measurement.

Accessories included:
Cuff for Non Invasive Blood Pressure.
Hose for Non Invasive Blood Pressure.


INVASIVE BLOOD PRESSURE (IBP) (OPTIONAL)
1 or 2 channels of invasive blood pressure, according to customer's choice.
Simultaneous measurement of Systolic, Diastolic and Mean pressure.
• Range: -30 to 300 mmHg.
• Mode selection for Pressure Ranges: Automatic or Manual.
• Mean Pressure alarm: minimum and maximum limits from -30 to 300 mmHg and off.
• Label: ART, AoP, LVP, PAP, CVP, WDG, RAP, RVP, ICP, IAP and IEP.
• Measure unit: mmHg.
CVP, ICP, IAP and IEP can measure in mmHg or cmH20.

TEMPERATURE (OPTIONAL)
2 channels of temperature.
Compatible with Thermistor Series YSI 400.
Measurement of body temperature or injectate temperature during measurement of Cardiac Output, from -5ºC to 45ºC.
• Resolution: 0.1ºC.
• Accuracy: ±0.2ºC.
• Temperature Alarm, minimum and maximum: -5ºC to 45ºC and off.

Accessories included:
Feas Electrónica temperature sensor - DB9M / G.
Derivation box for Temperature 1 and Temperature 2 parameters, DB9M connector (for two Temperature channels).

CARDIAC OUTPUT (OPTIONAL)
• Entry of patient parameters: Weight, height.
• Selection of:
- Injection volume: 3, 5 and 10 ml.
- Catheter Constant K or Computing Constant (CC)
- Measurement of the temperature in blood and injected.
• Calculation of:
- Body surface.
- CO: Volume in liters / min.
- SV: Stroke volume.
- CI: Cardiac index.
- SI: Systolic index.
Waveform graph for blood temperature as a function of time.
Manual or automatic start of the measurement when injecting.

Accessories included:
Catheter adapter cable for cardiac output - DB9M/G
Derivation box for parameters Temperature 1 and Cardiac Output with DB9.
Derivative box for parameters Temperature 1, Temperature 2 and Cardiac Output with DB9.

SIDESTREAM CAPNOGRAPHY (OPTIONAL)
Measurement of EtCO2, FiCO2 and Respiratory Rate.
• Range:
- CO2, from 0 to 100 mmHg (0% to 13%).
- Respiratory Rate, 4 to 170 1 / min.
• Accuracy:
- CO2, ± 2 mmHg for CO2 <5%.
- <10% of reading for CO2> 5%.
• Resolution:
- CO2, 1 mmHg.
- Respiratory Rate, 1 1 / min.
• Alarm:
- FiCO2, EtCO2, minimum and maximum, 0 to 100 mmHg and off.
- Minimum and maximum Respiratory Rate, 0 to 170 1 / min and off.
Calibration: 2 zero points (ambient air) and gain (5% or 10%).
Compensation for temperature and atmospheric pressure, O2 and N2O.

Accessories included:
Type "T" nozzle for Feás Electrónica lateral flow capnography.
2.4 m patient line for Feás Electrónica lateral flow capnography
Moisture filter for lateral flow capnography, Feas Electrónica

SIDESTREAM CAPNOGRAPHY WITH ANESTHETIC GASES MEASUREMENT (OPTIONAL)
Measurement of EtCO2, FiCO2 and Respiratory Rate.
• Range:
- CO2, from 0 to 100 mmHg (0% to 13%).
- Respiratory Rate, 4 to 150 1/min.
• Accuracy: CO2, ±3%ABS.
• Resolution: CO2, 1 mmHg.
- Respiratory Rate, 1 1/min.
• Alarm: FiCO2, EtCO2 minimum and maximum, 0 to 100 mmHg and off.
• Respiratory Rate minimum and maximum, 0 to 150 1/min and off.
• Measurement of N2 O: from 0% to 100%.
•Automatic detection and measurement of up two anesthetic gases: Halothane, Enflurane,Isoflurane, Sevoflurane and Desflurane.
- Range: 0% to 30%.
- Accuracy: ±8%REL.
- Resolution: 0.1%.
Flowrate:
- 70 to 120 ml/min for neonatal patients.
- 120 to 250 ml/min for adult patients.

Accessories included:
"T" type nozzle for sidestream Capnography, Feas Electrónica.
2,4 m patient line for sidestream Capnography, Feas Electrónica
Water trap for use in lateral flow capnography and anesthetic gases.

MAINSTREAM CAPNOGRAPHY (OPTIONAL)
Measurement of EtCO2, FiCO2 and Respiratory Rate.
• Range:
- CO2, from 0 to 100 mmHg (0% to 13%).
- Respiratory Rate, 4 to 150 1 / min.
• Accuracy: ± 2 mmHg between 0 and 40 mmHg and ± 5% of reading 41 and 70 mmHg.
• Resolution: 1 mmHg.
• Calibration: only zero (ambient air).
Compensation for temperature and atmospheric pressure, O2 and N2O.
Warm-up time <15s, to start measuring, within 2 minutes and obtain measurement values according to specifications.
• Waveform response time: less than 60 ms.

Accessories included:
Mainstream Capnography sensor, Feas Electrónica
Nozzle for mainstream Capnography sensor

FiO2 (OPTIONAL)
Fraction of inspired Oxygen: from 0% to 100%.
Polarographic cell measurement principle.
Alarms minimum and maximum: 0% to 100% and off.

Accessories included:
Derivative box for pressure 1, pressure 2 and / or FiO2 parameters with DB9M.
FiO2 Sensor, Feas Electrónica.
Disposable Oxygen Sensor T-adapter for FiO2, Feas Electrónica
Spiral cable of Oxygen Sensor for FiO2, Feas Electrónica.

ANY OTHER OPTIONAL CHANNEL SPECIFIED CAN BE ADDED IN THE FUTURE.

TECHNICHAL SPECIFICATIONS
15” LCD-TFT Color Monitor
• Resolution: 1024x768.
Wide angle of visibility.
• Dimensions:
- Height: 345mm; Width: 335mm; Depth: 205mm.
• Weight: 6Kg.
• Power Supply: 90V~ to 240V~ (with automatic voltage selection) 50Hz or 60Hz.
• Power Consumption: 85VA.

CERTIFICATIONS
• Quality Standard (Certificates):
- ISO 13485.
- Disp. A.N.M.A.T. 3266/2013: B.P.F.
- Disp. A.N.M.A.T. 2319/02.

• Safety Standard (Certificates):
- UNE-EN60601-1.(Eq. IRAM 4220-1 and IEC 601-1).
- Electrical-shock protection: Class I – CF.
- UNE-EN60601-1-2 (Electromagnetic compatibility).
Authorized by A.N.M.A.T.: PM 1125-2.

ACCESSORIES
Included:3 or 5 leads patient cable.
Disposable electrodes.
SpO2 sensor.
SpO2 extension cable.
Cuff for NIBP.
Silicone hose for NIBP.
Temperature sensor Feas Electrónica - DB9M/G.
Derivation box for parameters of Temperature 1 and Temperature 2, DB9M connector.
FiO2 Sensor Feas Electrónica.
T Adapter for FiO2 sensor Feas Electrónica.
Spiral cable for FiO2 sensor Feas Electrónica.
Power cord.
User manual.
The image is illustrative.

The images shown are for illustrative purposes only and may differ from the actual product. Specifications are subject to change without notice.
Automatic External Defibrillator (AED) Feas Electrónica, model: Heart+ ResQ NT-381.C
Heart + ResQ NT-381.C is an AED (Automatic External Defibrillator) that provides defibrillation treatments for the rapid resuscitation of the patient in SCA (Sudden Cardiac Arrest). This product is portable, battery operated. It is lightweight and can be operated even by users who have received little or no education / training on the use of the product, through voice prompts that guide the user through the operating sequences.

SCA (Sudden Cardiac Arrest) is the cessation of normal blood circulation due to heart failure. SCA can happen to anyone, anytime, anywhere. Patients with SCA do not show any warning signs or previous symptoms. Some are at higher risk for SCA than others, due to hereditary causes or other reasons.

GENERAL CHARACTERISTICS
Defibrillator
• Waveform: truncated exponential biphasic.
• 150 J (Adult, impedance 50 Ω).
• 50 J (Pediatric, impedance 50 Ω).
Charging time: 9 seconds (± 10 %).
• Shock method: manual button (flashes when ready).
• Mode conversion: Adult/Child toggle button.
(Child Mode delivers 50J Pediatric shock for patients weighing less than 25 Kg, approximately 12 months to 8 years old).

ECG
• ECG record: LEAD II.
• Analysis overview: Patient evaluated to determine whether ECG rhythm represents shockable or non-shockable state. Shockable rhythms are ventricular fibrillation.
• Analysis time: Approximately 7 seconds.

Battery Check
• Battery reserve level:
High: 3 bars.
Medium: 2 bars.
Low: 1 bar, red status led.
Critical: no bars, red status led.
• Battery status audible warnings.
Critical: Voice prompt states “Replace the battery”.

Data
• Stored data: ECG recordings, operation information (whether power is delivered or not), ambient noise, self diagnostic history.
• Memory capacity:
- ECG: Consecutively make records during analysis and CPR (once in every 5 s, up to 5000 s).
- Audio recording: 60 min in total (4 recording files of 15 min).
- Self-diagnosis: 3000 cases and results.
• Storage type: Internal memory.
• Access/search: “NT-ADV” software (for PC), via Bluethooth.

Audible and Visual Instructions
• After the equipment is switched on, the voice instructions will guide the operator through the resuscitation process, including the positioning of the patches, the indication of “Don’t touch the patient” (during the energy analysis and discharge process) and CPR (Cardio-Pulmonary Resuscitation) instructions.
• The CPR instructions tell the operator when to start Cardio-Pulmonary Resuscitation, according to the AHA Guide.

TECHNICAL SPECIFICATIONS
• Dimensions: 220 mm (W) x 282 mm (L) x 80 mm (H).
• Weight: 2 Kg (including battery and pads).
• Internal non-rechargeable Li-MnO2 battery - 12 Vdc/4200 mAh.
• Protection against ingress of liquids: IPX5 according to IEC60529.
• Temperature:
Storage: 15 ºC to 55 ºC.
Operation: 0 ºC to 45 ºC.
• Humidity:
Storage: 0 % to 95 % (without condensation).
Operation: 0 % to 90 % (without condensation).
• Altitude (Storage/Operation): 0 to 5000 meters.
• Drop test: 1.5 m according to IEC 60068-2-32.
• Quality standards:
ISO 13485 (certified).
Available A.N.M.A.T. 3266/2013: B.P.F.
Available A.N.M.A.T. 2319/02.
• Safety standards:
- IEC 60601-1 (Eq. IRAM 4220-1 and IEC 601-1).
- IEC 60601-1-2 (Electromagnetic Compatibility).
- IEC 60601-1-6.
- IEC 60601-1-11.
- IEC 60601-2-4.

ACCESSORIES INCLUDED
- Electrode pads
• Shelf life: 2 (two) years.
• Single use.
• Cable length: 2.1 m (± 1 %).
• Applicable ages: All ages (12 months & older).
• Sealing: Airtight.
• Size: 125 mm x 95 mm.
• Pads placement:
Adult: anterior-lateral.
Pediatric: anterior-posterior (see positioning details on the package label).
- 1 Battery Pack
• Type: non-rechargeable Lithium-Manganese Dioxide (Li-MnO2).
• Voltage: 12 Vdc/4200 mAh.
• Standby mode life: Recommended five (5) years at 25 ºC.
• Capacity: 180 shocks @ 25 ºC, 130 shocks at 0 ºC.
• Measures: 22 mm (H) x 164 mm (W) x 54 mm (D).
• Weight: 260 g (±10 %).
- 1 User manual
- 1 bag
- Event Reading Software

OPTIONAL
USB/Bluetooth adapter.


The images shown are for illustrative purposes only and may differ from the actual product. Specifications are subject to change without notice.
Infusion Pump model SN-1500H, Sino MDT Ltd.
Infusion pump of volumetric type with peristaltic perfusion system that accepts universal type set. Comprehensive and effective solution to optimize infusion therapy in all the units of the Hospitals and Health Centers.

• Great quality. Easy to use. Menu in Spanish.
• It has a simple system to calibrate different sets of infusion and can be recorded up to 9 calibrations for different sets.
• It has a horizontal structure with an effective prevention against the entry of liquids. It can be hung from the serum support or placed on a table or car.
• High accuracy, due to an intelligent pulsating compensation made by a double micro-processed unit, resulting in a constant flow of high precision infusion.
• It has five types of infusion mode: Speed ​​mode, Drip mode, Body Weight mode, Time mode and Drug mode.
• Contains drip sensor.
• Contains ultrasonic bubble sensor, high sensitivity.
• It contains a pressure sensor that allows adjustment of 3 levels of occlusion pressure.
• High definition screen, allows the on-screen display of the controlled / running function.
• Illuminated alarm panel (up to 12 alarms). Interface for nurse call.
• Record of 1500 historical events.
• The following features and functions contribute to make the patient's treatment more pleasant:
• Preheating function of the infused solution, with constant temperature of the solution.
• When the pump door is opened, in a dark environment, a light is switched on automatically that allows changing the set or working on the infusion pump without turning on the ambient light.
• Silent operation and without vibrations, because it is equipped with a high quality motor.
• External DC power supply input, also works with 12 VDC input.
• Easy to transport due to its small size and weight (2.5 kg).

TECHNICAL SPECIFICATIONS
Specification of IV set: 20 drops / ml or 60 drops / ml.

Infusion flow rate:
•Set IV of 20 drops / ml:
0.1ml / h ~ 1500ml / h.
1 drops / min ~ 350 drops / min.
• Set IV of 60 drops / ml:
0.1ml / h ~ 200ml / h.
1 drops / min ~ 200 drops / min.
• When the speed is between 0.1ml / h ~ 99.9ml / h, the infusion flow rate is changed from 0.1ml / h.
• When the speed is above 100ml / h, the infusion flow rate is changed from 1ml / h.
• Accuracy: ± 5%.

Bubble Detector:
• Ultrasonic detection method: bubbles are detected above 25μl.

- Occlusion warning speed:
It can be divided into three ranges as indicated,
- High (H) 900mmHg ± 200mmHg (120kPa ± 26,7kPa).
- Central (C) 500mmHg ± 100mmHg (66,7kPa ± 13,3kPa).
- Low (L) 100mmHg ± 50mmHg (13.3kPa ± 6,6kPa).
• Flow rate of the Purge Bolus:
Adjustable between 600ml / h ~ 1000ml / h.
• Kvo rate (to maintain permeable route):
Adjustable minimum flow between 0.1ml / h ~ 5ml / h.

Built-in battery:
• Ni-Mh, 12 Vdc, 2300 mAh, the recharge cycle can be repeated up to 500 times.
• Operating time of the battery: with the battery fully charged, it can run continuously for more than 5 hours at a speed of 25ml / h.

Operation mode:
Keep going.

Protection against the ingress of liquids: IPX4 - Protected against splashing water in any direction.

Historical records:
You can store the historical records of more than 1500 infusions made.

Communication link: SN-1500H: RS-232.

• Supply voltage: 110V ~ to 230V ~ - 50Hz or 60Hz or 12Vcc-5A external.
• Maximum power: 40 VA.
• Classification: class I and internally powered.
• Protection against electric shocks: Type CF.

WORK ENVIRONMENT:
Operating conditions:
• Ambient temperature: + 5ºC to + 40ºC.
• Relative humidity: 20% to 90%.
• Atmospheric pressure: 645mmHg (86kPa) to 795mmHg (106kPa).
Storage conditions:
• Ambient temperature: -5ºC to + 55ºC.
• Relative humidity: 0% to 95%.
• Environmental pressure: 500mmHg (66,7kPa) to 797mmHg (106,3kPa).

ACCESSORIES INCLUDED
1 Power cable to line.
1 user manual.

CERTIFICATES
• Certified Quality Standard:
ISO13485.
Disp. A.N.M.A.T. 3266/2013: B.P.F.
Disp. A.N.M.A.T. 2319/02.
• Safety rules:
IEC 60601-1 (Eq IRAM 4220-1 and IEC 601-1- Req.
IEC 60601-1-2 (Electromagnetic Compatibility).
IEC 60601-2-24 (Infusion Pumps).

FREQUENT QUESTIONS
Do you use any brand of infusion set?
Yes, the pump is not dependent on any brand of supplies. It is recommended that the silicone IV Set be used.

Can it be used on animals?
Yes, it can be used on animals.

The images shown are for illustrative purposes only and may differ from the actual product. Specifications are subject to change without notice.
Infusion Pump model SN-1800V, Sino MDT Ltd.
Infusion pump of volumetric type with peristaltic perfusion system that accepts universal type set. Comprehensive and effective solution to optimize infusion therapy in all the units of the Hospitals and Health Centers.

• Great quality. Easy to use. Menu in English.
• It has a simple system to calibrate different sets of infusion and can be recorded up to 12 calibrations for different sets.
• It has a vertical structure with an effective prevention against the entry of liquids. It can be hung from the serum support or placed on a table or car.
• High accuracy, due to an intelligent pulsating compensation made by a double micro-processed unit, resulting in a constant flow of high precision infusion.
• It has six types of infusion mode: Speed mode, Drip mode, Body Weight mode, Time mod, Infusion Plan and Drug Library or Drug Mode.
• Contains drip sensor.
• Contains ultrasonic bubble sensor, high sensitivity.
• It contains a pressure sensor that allows adjustment of 10 levels of occlusion pressure.
• High definition screen, allows the on-screen display of the controlled / running function.
• Illuminated alarm panel (up to 12 alarms). Interface for nurse call.
• Record of 1500 historical events.

The following features and functions contribute to make the patient's treatment more pleasant:
• When the pump door is opened, in a dark environment, a light is switched on automatically that allows changing the set or working on the infusion pump without turning on the ambient light.
• Silent operation and without vibrations, because it is equipped with a high quality motor.
• External DC power supply input, also works with 12Vdc input.
• Easy to transport due to its small size and weight.
• Interface USB.

TECHNICAL SPECIFICATIONS
Specification of IV set: 20 drops/ml or 60 drops/ml.

Infusion flow rate:
• Set IV of 20 drops/ml: 0.1ml/h ~ 1500ml/h.
• Set IV of 60 drops/ml: 0.1ml/h ~ 1500ml/h.
• When the speed is between 1ml/h ~ 99.9ml/h, the infusion flow rate is changed from 0.1ml/h.
• When the speed is above 100ml/h, the infusion flow rate is changed from 1ml/h.
• Accuracy: ± 5%.

Bubble Detector:
Ultrasonic detection method: bubbles are detected above 25μl.

Occlusion pressure value:
• Ten adjustable levels, with an error of ± 50mmHg or ± 25% (6.6KPa).
• Adjustment range: from 100mmHg (13.3KPa) to 900mmHg (120KPa).
Flow rate of the Purge Bolus:
• Adjustable between 5ml/h ~ 1000ml/h.
Kvo rate (to maintain permeable route):
• Adjustable minimum flow between 1ml/h ~ 5ml/h.

Built-in battery:
• Ni-Mh, 12 Vdc, 2300 mAh, the recharge cycle can be repeated up to 500 times.
• Operating time of the battery: with the battery fully charged, it can run continuously for more than 6 hours at a speed of 5ml/h.

Operation mode: Continuous.

Protection against the ingress of liquids: IP32.

Historical records:
You can store the historical records of more than 1500 infusions made.

Communication link: SN-1800V: RS-232.

• Supply voltage: 100V ~ to 240V ~ / 50Hz or 60Hz or 12Vdc external.
• Maximum power: 28 VA.
• Classification: class I and internally powered.
• Protection against electric shocks: Type CF.

Work environment:
• Operating conditions:
Ambient temperature: + 5ºC to + 40ºC.
Relative humidity: 20% to 90%.
Atmospheric pressure: 645mmHg (86kPa) to 795mmHg (106kPa).
• Storage conditions:
Ambient temperature: -20ºC to + 55ºC.
Relative humidity: 0% to 95%.
Environmental pressure: 375mmHg (50kPa) to 795mmHg (106kPa).

Weight: 1,8Kg.

Dimensions: 129mm x 130mm x 215mm (Width x Length x Height).

ACCESSORIES INCLUDED
1 Power cable to line.
1 user manual.

CERTIFICATES
• Certified Quality Standard:
ISO 13485.
Disp. A.N.M.A.T. 3266/2013: B.P.F.
Disp. A.N.M.A.T. 2319/02.
• Safety Standard:
IEC 60601-1 (Eq IRAM 4220-1 and IEC 601-1- Req.
IEC 60601-1-2 (Electromagnetic Compatibility).
IEC 60601-2-24 (Infusion Pumps).

FREQUENT QUESTIONS
Do you use any brand of infusion set?
Yes, the pump is not dependent on any brand of supplies. It is recommended that a silicone IV Set be used.

Can it be used in animals?
Yes, it can be used in animals.

The images shown are for illustrative purposes only and may differ from the actual product. Specifications are subject to change without notice.
Emergency trolley CP 2000 Feas Electrónica
Designed to give first aid to patients in an emergency state.
Easy to use and reconfigure.
Sliding shelf that allows to support writing paper-
Drawer key system with total closure.
High degree of storage efficiency and mobility.
Each drawer contains a basket of ABS with partitions that allow an optimal organization of the space.
Four wheels of 13 cm, two of them with brakes.
Dimensions: height: 120 cm, width: 90 cm, depth: 60 cm.
Weight: 60 kg.
Uses: Not suitable for MRI room.

The images shown are for illustrative purposes only and may differ from the actual product. Specifications are subject to change without notice.
Odontology Implant System
· It is intended to be used in Dental Implants, in all its stages, and in all types of patients.
· This equipment has been design following international standards, in terms of perfomances and functions.
· High quality motor and great torque, free of vibrations.
· By using a key, you can access the maximum torque selection applied to the tool, between 5 and 45 N cm, or disabled.
· Its adjustable electronic torque meter differentiates it from other equipment.
· Both speed and torque are relative to the selected Reduction. Handpiece reduction: 16:1, 20:1 and 32:1, and digital speed selection, displayed on the display.

MULTIFUNCTION FOOT CONTROL

· Hands-free device for control and programs.
· Heavy multifunction foot control for high stability.
· Main control: It starts the motor in progressive mode (linear) mode or it can be programmed to operate as on/off mode.
· Function: When pressed once, it alternates from one to the other. While holding down, navigate between the three programs of each function.
· Turn: The micro motor tool has the possibility of inverting its rotation, using the DIRECT/REVERSE button on the keyboard, or "Turn" in the multifunction foot control.
· The reverse direction of rotation is indicated on the screen and by an audible tone.
· Pump: Press once, it will turn ON or OFF, when turns ON recalls the last flow rate. Keeping pressed, increase the flow; Off, On 25, On 50, On 75, On 100, Off. This is being represented on the display with 1, 2, 3, or 4 drops.

PERISTALTIC PUMP

Is located in the back of the equipment. Supply 15 ml/min to 45 ml/min for jobs that require it.

CONTENTS

- 1 Main Unit Control.
- 1 Main Power Cable.
- 1 Multifunction Foot Control.
- 1 Brushless Micromotor.
- 1 Sterilisable Headpiece Holder.
- 3 Set Irrigation Tubes.
- 1 User's Manual.
(Handpieces are not included).

TECHNICAL SPECIFICATIONS

Unit Control:
- Global Size: 270mm x 115mm x 230mm.
- Power Input: 90Vac-240Vac 50/60Hz (Automatic).
- Line Fuse: 2.5A/250V, 5mm x 20mm SB.
- Nominal Power: 3W.
- Maximum Power: 150W.
- Screen: LCD - 5.5" (High Luminosity).
- Weight: 2Kg.

Pump:
- Type: Peristaltic with 3 rollers.
- Flow: 15-45ml/min including off.

Multifunction Foot Control:
- Global Size: 18mm x 13.5mm x 43mm.
- Weight: 1.65Kg.
- Protection grade: IPX4.

Motor:
- Rate: 500rpm, 50000 max.
-Torque: 5 to 45 N.cm.



















The images shown are for illustrative purposes only and may differ from the actual product. Specifications are subject to change without notice.
Multi uses trolley Model CT62512D3T Feas Electrónica
PRODUCT DESCRIPTION

Rolling unit ideal for use in clinics, sanatoriums, hospitals and health centers in general. Allows organized storage of supplies and placement of equipment on the top shelf
Multipurpose trolley.
Top shelf with protective railing and transparent cover.
Sliding ABS drawer, with internal compartments that allow efficient organization of supplies.
ABS middle shelf.
Bottom shelf made of ABS.
Material: ABS, high impact engineering plastic.
2 garbage cans with lid
4 silent wheels of 13 cm, 2 of them with brakes.
Warranty: 1 year.
Aluminum structure covered with ABS plastic, material resistant to rust and corrosion.

The images shown are for illustrative purposes only and may differ from the actual product. Specifications are subject to change without notice.
Electrophysiology and hemodynamic polygraph system mod. 1405 Feas Electrónica
The Polygraph is a system for conducting electrophysiology and hemodynamic studies.

The system is intended to be used in the acquisition, processing and recording of physiological signals. This includes surface electrocardiography (ECG) and intracavitary (IECG, for Electrophysiology only), heart rate, pulse oximetry (optional), invasive and non-invasive pressure (optional), cardiac output and hemodynamic calculations, now the last two for Hemodynamics only.

It is made up of a central data processing unit (CPU), a preamplifier, a color monitor, a laser printer, a keyboard, a mouse and a recording pedal. For Electrophysiology (if applicable), the Polygraph catheter extension box is added.

FEATURES

Hemodynamics
- 2 simultaneous ECG leads on screen, selectable from 12 leads using 10 electrode wires.
- Up to 4 Invasive Pressures.
- Automatic calculation of the fractional flow reserve (FFR) in real time, without the need for an independent (external) FFR analyzer. The FFR allows determining the hemodynamic severity of vascular lesions.
- Numerical and graphic display of the FFR value.
- Study storage.
- Cardiac output by thermodilution. Calculation of BSA, CO, CI, SV, SI.
- Selection of Catheter Constant K.
- Selection of the injection volume.
- Entry of patient data (height and weight).
- Measurement of the temperature of the blood and the injected.
- Curve of blood temperature variation.
- Messages on screen.
- Recording of studies, stores curves and calculations.
- Measurement of body or injection temperature (during cardiac output).
- Allows you to freeze curves and measure times and amplitudes using calipers.
- Printing of frozen curves or recorded studies.
• HEMODYNAMIC CALCULATIONS:
- Aortic valve area.
- Pulmonary valve area.
- Calculation of pulmonary and systemic vascular resistance.

ELECTROPHYSIOLOGY (OPTIONAL)
- 18 simultaneous endocavitational channels.
- Calipers on Screen: allow you to measure time between events of interest.
- 12 simultaneous surface ECG leads.
- Up to 4 Invasive Pressures.
- Tabular presentation of P.N.I.
- Split Screen: allows you to have a frozen reference image in one window, and in the other view the monitoring in real time.
- Quick access to the curve configuration window, where you can make a continuous selection of position, amplitude, filter selection and customize colors and labels of curves.
- Synchronized triggering of the curve sweep (trigger).
- Recording Studies on a hard disk, to be transported to other computers or personal computers using a pen drive.
- One SpO2 channel.
- Study printing with selection of color and line width.
- Catheters connection box and Cardiac Stimulator
- Review of recorded studies, with the possibility of modifying the gain, position, color and limits (of amplitude) of the curves.
- Quick access keys.

Pulse Oximetry (OPTIONAL)
- Plethysmographic curve, visualization of the oxygen saturation percentage.
- Low perfusion and movement signal measurement.
• SpO2:
- Range from 0% to 100%.
- Adult Accuracy: 2% from 70% to 100%.
- Neonatal Accuracy: 3% from 70% to 100%.
- Accuracy in motion: 3% from 70% to 100%.
- Resolution: 1%.
• Pulse Rate:
- Range from 20 [1 / min] to 300 [1 / min].
- Adult Accuracy: ± 3 [1 / min].
- Neonatal precision: ± 3 [1 / min].
- Accuracy in movement: ± 5 [1 / min].
- Resolution: 1 [1 / min].

Non-Invasive Pressure (OPTIONAL)
- Start of measurement manually or automatically at programmable intervals from 2 minutes to 90 minutes.
- Selection of Adult or Neonatal patient.
- Visualization of the last 1440 measurements.
- Printing of measurements in tabular form.
- Includes cuff.

TECHNICAL SPECIFICATIONS
• Screen: LCD monitor 19 ”
- Dimensions: 19 ”(larger size; optional)
- Resolution: 1024 x 768 dots
•CPU:
- Industrial PC motherboard.
- 160 Gb hard disk.
- Output to connect an additional remote monitor.
• Printing machine:
- Laser Technology.
- Resolution 1200 dpi.
• Power supply:
- 110V ~ / 220V ~.
- Frequency 50/60 Hz.

• Quality Standard:
- ISO9001 (certified).
- ISO13485 (certified).
- Disp. A.N.M.A.T. 3266/2013: B.P.F. (certificate).
- Disp. A.N.M.A.T. 2319/02 (certified).

• Safety Standard:
- UNE-EN60601-1 (Eq. IRAM 4220-1 and IEC 60601-1) Class I.
- Protection against electric shock: CF.
- Authorized by the A.N.M.A.T. PM 1125-23.

ACCESSORIES INCLUDED
- Preamplifier for Hemodynamic Studies.
- Interconnection cable from CPU to Preamplifier.
- Monitor, keyboard and mouse.
- Cable "Y" Minidin-M to 2 Minidin-F.
- Printing machine.
- Recording pedal with cable.
- CPU, monitor and printer power cables.
- Data cable to printer.
- Ground cable for interconnection between CPU and Preamplifier.
- Metal support for Preamplifier.
- Catheter extension box.
- Interconnection cable for catheter extension box.
- Mini equipment holder.
- TMM Bracket Mounting Clamp for TBC.
- Support plate for 4 transducers.
- Power strip with 5 shots.
- Disposable electrodes.
- 4 disposable pressure transducers.
- 4 interconnection cables from Preamplifier to disposable pressure transducers.
- Parameter derivation box for invasive pressure
- Injection temperature sensor.
- Patient cable with 3, 5 or 10 wires.
- Cardiac output catheter adapter cable.
- Oximeter sensor.
- Oximeter extension cable.
- Reus Adult Cuff.
- Silicone hose for PNI, 3m.
- Digital adapter for pressure guides (FFR).
- Volcano Pressure Guide Adapter Cable (FFR).
- Transport trolley (optional).
- User manual.

The images shown are for illustrative purposes only and may differ from the actual product. Specifications are subject to change without notice.
Temporary Cardiac Pacemaker OSYPKA Dual Chamber Model PACE-203
The PACE Model 203 Dual Chamber (DDD) Temporary Cardiac Pacemakeris designed for safe and dependable temporary stimulation of the heart for peri/postoperative pacing and/or therapy for conduction defects and rhythm disturbances.

GENERAL CHARACTERISTICS
• Intuitive dial interface allows for fast and easy access to stimulation and sensitivity settings for the atrium and ventricle.
• High Rate funtion provides rapid atrial stimulation of up to 1,000 ppm (adjustable while applying rapid atrial stimulation).
• Just one button push to automatically measure atrial/ventriuclar rates and intervals, P/R wave amplitudes and AV interval.
• Statistical recording and analysis of pacer activity.
• Standard 9 V alkaline battery provides an average of 240 hrs of continuous operation.
• 2 year warranty.

ACCESSORIES
• Myocardial heartwires for temporary pacing (unipolar, bipolar, and quadripolar)
• Transvenous pacing leads for minimally invasive temporary pacing applications
• Extension cables for temporary pacing leads

TECHNICAL SPECIFICATIONS
Dimensions: 212 mm x 96 mm x 51 mm(8.3” x 3.8” x 2.0”).
Weight 490 g (17.28 oz) including battery
Battery Alkaline: 240 hrs (9.0 V)
Basic Rate 30 - 220 ppm
High Pacing Rate 70 - 1000 ppm
Stimulation Amplitude 0.1 - 18 V
Pulse Width 0.05 - 1.5 ms
Sensitivity Atrium: 0.02 - 20 mV
Ventricular: 1.0 - 20 mV
Refractory Period 250 ms
Runaway Protection 200 ppm ±10 ppm
Pacing Modes:
- Primary: DDD, VVI, AAI, VDD
-Supplementary: D00, V00, A00, DVI
-DAI, VAT, AAT, DDD+AT, DAT




The images shown are for illustrative purposes only and may differ from the actual product. Specifications are subject to change without notice.
PACE-101 Single Chamber Cardiac Pacemaker OSYPKA
GENERAL CHARACTERISTICS
The PACE 101 single-chamber cardiac pacemaker has the reputation of a legendary workhorse - easy to operate, very durable and light weight. It is intended for temporary atrial or ventricular pacing and supports synchronous (VVI, AAI) and asynchronous (V00, A00) operating modes.

Features:
-Basic stimulation frequency up to 180 ppm.
-Large rotating dials for stimulation frequency, sensitivity, amplitude and pacing mode.
-Rapid atrial pacing up to 720 ppm.
-Long battery lifetime: up to 38 days of operation with a single 9V Alkaline battery.
-Four rotational dials for setup up stimulation frequency, amplitude, sensitivity, and pacing mode.
-Sensed intrinsic activity and paced pulses are indicated optically by a light-emitting diode (LED). Additionally, acoustic signals for sensing and pacing events can be switched on and off.
-Automatic surveillance of battery charge condition. Low battery status is indicated optically by a separate LED labeled 'Low Batt./Error' and acoustically by a warning beep.
-Internal error detection. A device error or defect is indicated by a separate LED labeled 'Low Batt./Error'.
-Run-away protection. The stimulation frequency is limited to a maximum of 180 ppm.
-Protective cover of dials. A protective cover safeguards against accidental changes to the device settings.
Protected terminals in combination with the Series XI Extension Cables ensure touch-proof connection of pacemaker and pacing lead system.

TECHNICAL SPECIFICATIONS
- Dimensions: 6 cm x 11.5 cm x 2.2 cm.
- Weight: 170 g (battery included).
- Alkaline battery: 38 days (72 ppm, 8V).
- Basic stimulation range: 30-180 ppm.
- Rapid stimulation range: basic range x2 or x4 (up to 720 ppm).
- Stimulation amplitude: 0.3 - 12 V.
- Pulse width: 0.75 ms.
- Sensitivity: 1.0 mV at 20 mV, asynchronous.
- Refractory period: 250 ms.
- Protection against uncontrolled running: 200 ± 10 [1 / min].
- Ways of marcapaseo: VVI, VOO, AAI, AOO.

INCLUDED ACCESORIES
- Extension cable.
- User's manual.
- Arm Strap.
- Plastic equipment bag.

OPTIONAL GADGETS
Myocardial heartwires for temporary pacing (unipolar, bipolar)•
Transvenous pacing leads for minimally invasive temporary pacing applications•
Extension cables for temporary pacing leads

The images shown are for illustrative purposes only and may differ from the actual product. Specifications are subject to change without notice.
Patient Monitor, Multiparameter, of 10,4", Comen, With Batery Li ion include, Touch screen, Light, model C50
C50 PATIENT MONITOR

C50 provides the physician with advanced functionalities and monitoring options in order to meet the demands of a wide range of care in any hospital environment.
It has a 10.4 "" color screen with TFT technology included to facilitate observation.
Easy use of the menu via rotary knob and touch screen.
In addition, it has reserved expansion ports for SD card, USB port and network.

Use Adult, Pediatric, Neonatal

ELECTROCARDIOGRAM (ECG)
Heart rate:
• Adult: 15-300 [1 / min]
• Neonates / children: 15 - 350 [1 / min]
Accuracy: ± 1% or ± 1 [1 / min], whichever is greater.
Resolution: ± 1 [1 / min]
Gain selection: 1.25mm / mV, 2.5mm / mV, 5.0mm / mV, 10mm / mV, 40mm / mV, Auto.
Manual replacement.
Automatic selection of cable to patient.
3, 5, 12-lead ECG input mode.
Lead selection:
1. DI, DII, DIII
2. DI, DII, DIII, aVR, aVL, aVF and V
3. DI, DII, DIII, aVR, aVL, aVF and V1 to V6
Frequency response:
• Monitoring mode: 0.5-40Hz.
• Diagnostic mode: 0.05-130Hz.
• Surgery mode: 1-20Hz.
• ST mode: 0.05-40hZ.
Heart rate alarms:
• Adult: 15 - 300 [1 / min]
• Neonates / children: 15 - 350 [1 / min]
Loose electrode detection.
Pacemaker Pulse Suppression Capability:
Amplitude of ± 2mV ~ ± 700mV and pulse width of 0.1ms - 2.0ms.

ANALYSIS AND CLASSIFICATION OF ARRHYTHMIAS
Arrhythmia Type: PVC, Asystole, VTac, Tachycardia, Ventricular Tachycardia, Supraventricular Tachycardia, VR, Bigemine, Trigemine, R over T, Bradycardia, Ventricular Bradycardia, Missed Beats, Atrial Fibrillation, Ventricular Fibrillation, Pacemaker Not Captured (PNC) Pacemaker does not dial (PNP).
ST segment analysis:
Range: -2mV to + 2mV
Accuracy: Measurement tolerance within (-0.8 mV) - (+ 0.8 mV) is ± 0.02 mV or ± 10%, whichever is greater. It is not defined for other ranges.
Resolution: 0.01mV (0.1mm)

OXYGEN SATURATION
Plethysmographic curve, arterial oxygen saturation (SpO2) values, peripheral pulse rate (FFPP) and pulse intensity bar.
COMEN SpO2:
Range: 0% - 100%
Adult/Child Accuracy: Within 70% -100%, tolerance is ± 2% (no movement).
Neonatal Accuracy: Within 70% -100%, tolerance is ± 3% (no movement).
Resolution: 1%
Alarm: 0% to 100%

PULSE FREQUENCY
COMEN SpO2:
Range: 20 - 254 [1 / min]
Resolution: 1 [1 / min]
Accuracy: ± 2 [1 / min]
Alarm: 20 to 350 [1 / min]

RESPIRATORY CURVE
Impedance method.
Breathing frequency:
• Adult monitoring range: 0 to 120 [1 / min]
• Monitoring range for child/neonate: 0 to 150 [1 / min]
Within 7 [1 / min] - 150 [1 / min], the measurement error is ± 2 rpm or ± 2%, whichever is greater.
Tolerance is not defined by other ranges.
Alarm limit specifications:
• Adult monitoring range: 0 to 120 [1 / min]
• Monitoring range for child / neonate: 0 to 150 [1 / min]
Apnea alarm

NON-INVASIVE PRESSURE
Automatic Oscilometric Method
Measurement mode: Manual, auto (cyclical) or continuous (not suitable for neonates)
Unit of measure: mmHg
Nominal monitoring range:
• Adult Range:
Systolic: 40 - 270 mmHg,
Diastolic: 10 - 215 mmHg,
Medium: 20 - 235 mmHg
• Pediatric Range:
Systolic: 40 - 200 mmHg,
Diastolic: 10 - 150 mmHg,
Medium: 20 - 165 mmHg
• Neonatal Range:
Systolic: 40 - 135 mmHg,
Diastolic: 10 - 100 mmHg,
Medium: 20 - 110 mmHg
Alarm limit specifications:
• Adult Range:
Systolic: 40 - 270 mmHg,
Diastolic: 10 - 215 mmHg,
Media: 20 - 235 mmHg
• Pediatric Range:
Systolic: 40-200 mmHg,
Diastolic: 10 - 150 mmHg,
Media: 20-165 mmHg
• Neonatal Range:
Systolic: 40 - 135 mmHg,
Diastolic: 10 - 100 mmHg,
Media: 20 - 110 mmHg
Precision:
The mean error must be less than 5 mmHg
The standard deviation must be less than 8 mmHg.
Manual or automatic start of measurement at programmable intervals of 1/2 / 2.5 / 3/4/5/10/15/30/60/90/120/180/240/480 / 720min.
Measurement time under continuous mode: 5 min
Overpressure protection:
• Adult: When the cuff pressure exceeds 297 mmHg ± 3mmHg, the control valve will relieve the pressure.
• Child: When the cuff pressure exceeds 240 mmHg ± 3 mmHg, the control valve will relieve the pressure.
• Neonate: When the cuff pressure exceeds 147 mmHg ± 3mmHg, the control valve will relieve the pressure.
Resolution: 1 mmHg.

TEMPERATURE
Measurement method: direct.
A temperature channel.
Temperature ranges
Range: 0 - 50 ° C
Accuracy: ± 0.1 ° C (probe tolerance only)
Resolution: 0.1 ° C
Maximum and minimum temperature alarms:
Range: 0 - 50 ° C

TECHNICAL SPECIFICATIONS
10.4 "color touch screen with TFT technology Resolution: 800 X 600
Tilted screen for easy observation.
Dimensions: 291.7mm x 250mm x 146.5mm
Weight 3.3 Kg. With battery
Power supply: It has an internal battery and an external AC.
Supply voltage:
100 - 240 Vac, 50/60 Hz.
C50: Standard: Li-Ion 11.8 V / 2200 mAh.
Once fully charged, it ensures continuous autonomous operation for 2 consecutive hours.
Consumption: 60 VA

Reserved expansion ports for SD card, USB port and network.
Quality standards:
IEC 60601-1, IEC 60601-1-8, IEC 60601-2-27, EN 1060-3, IEC 80601-2-30, IEC60601-2-34, IEC60601-2-49, ISO 80601-2-56, ISO 80601-2-61, Class 1, IPX1.

OTHER PRODUCT NAMES
Multi-Parameter Monitor / Patient Monitor / Vital Signs Monitor / Cardiomonitor

FREQUENT QUESTIONS
Can it be used in animals?
Yes, please let us know when buying and we will make the adaptation of the accessories.


The images shown are for illustrative purposes only and may differ from the actual product. Specifications are subject to change without notice.
Patient Monitor, Multiparameter, Comen Model C30
The COMEN C30 Multi-Parameter Patient Monitor is the perfect device to meet all your portable monitoring needs in and out of the hospital. In addition, its hardness and quality allow it to withstand a 1.2 meter drop, making it an excellent portable device that meets the needs of all hospitals. Created for use in adult, pediatric and neonatal patients. It can provide users with all the basic monitoring parameters required by their patients.
Strong, stable, waterproof, dustproof, anti-drop and shockproof.
Small and light, easy to carry.
Suitable for emergency scene, out-of-hospital transport, intra-hospital transport, bedside monitoring in the emergency department

Model C-30
Technical specifications
Security
ISO 13485: 2003 Approved
CE marking according to MDD93 / 42 / EEC

Physical characteristics:
Dimensions: 190mmX81.6mmX107mm
weight: 1.2 kg

Operation Environment
Power: 15Vdc
Power supply: 100-250Vac, 50/60 Hz.
Temperature: 0-40 ° C
Humidity: 15-85%
Battery: Lithium-ion, rechargeable
Plug & play battery, capacity: 2600mA
Maximum of 6.5 hours for charging;
4 hours of continuous work

Specifications
Patient: adult, pediatric, neonate
Display: 4.3 "color TFT touch screen
Resolution: 16:9
2 curves on screen
Sweep speed: 12.5mm / s, 25mm / s, 50mm / s
Indicators:
• Battery indicator light
• Dual indicator alarm light
QRS beep and alarm sound
Key sound
AC input socket
MDR
Trend: 48 hours
Alarm: user adjustable high and low limits
Connection to the monitoring center
DVI connection

Breathing
Impedance method
Rate:
• Adult 0-1OOrpm
• Neonatal 0-150 rpm
• Resolution: ± 1 rpm
Apnea alarm: 10s-40s
Audible and visual alarm
Sweep speed: 12.5.25mm/s
Gain selection: x0.25, x0.5, x1, x2

ECG
Cable: 12-lead CardioTecTM,
3 or 5 snaps (selectable)
12 leads: I, Il, III, aVR, aVL, aVF, V1, V2, V3, V4, V5, -V6
5 wire: RA, LA, RL, LL, V or R, L, N, F, C,
3 wire: RA, LA, LL or R, L, F
Lead Selection: 12 leads: I, II, III, aVR, aVL, aVF, V1, V2, V3, V4, V5, V6
5 wire: I, Il, IIl, aVR, aVL, aVF, V
3 wire: I, Il, III
Gain selection: x0.25, x0.5, x1, x2, auto
Adult: 15-300 1 / min
Pediatric / neonate: 15-350 1 / min
Accuracy: ± 1% or ± 1 1 / min (whichever is greater)
Resolution: 1 1 / min
ECG bandwidth:
MON: 0.5-55Hz
DIA: 0.05-150 Hz
OPE: 1-20Hz
ST segment detection: ± 2.0mV (automatic)
Arrhythmia Analysis
Pacemaker pulse detection

Temperature
2 channels
Standard sensor: Cutaneous
Measurement range: 0-50 ° C
Resolution: 0.1 ° C
Accuracy: 0.1 ° C (excludes sensor error)
Channel: T1, T2, TD (temperature difference)

PNI
Measurement method: Automatic oscillometric
Working mode: manual / automatic / continuous
Interval: Adjustable from 1 min to 480 min
Measurement types: systolic, diastolic, mean
Unit of measure: mmHg / KPa, adjustable
Systolic pressure range:
• Adult: 40 to 270 mmHg
• Pediatric: 40 to 200mmHg
• Neonate: 40 to 135 mmHg
Diastolic pressure range:
• Adult: 10 to 215 mmHg
• Pediatric: 10 to 150mmHg
• Neonate: 10 to 100 mmHg
Medium pressure range:
• Adult: 20 to 235 mmHg
• Pediatric: 20 to 165mmHg
• Neonate: 20 to 110 mmHg
Overpressure Protection: Hardware and Software
• Accuracy: less than ± 5mmHg
• Resolution: 1mmHg

Sp02 Comen
Range: 1-100%
Resolution: 1%
Accuracy:
• ± 2% (70-100%, Ped, no movement)
• ± 3% (70-100%, Neo, no movement)
• 0-69% unspecified
Range alarm: 0-100%
Pulse Frequency:
• Range: 20 to 300 ppm
• Resolution: 1 ppm
• Accuracy:
- ± 3ppm (no movement)
- ± 5ppm (movement)
Alarm: 20 to 300 ppm

EtCO2
Sidestream CO2 (SideStream)
Range: 0 to 150 mmHg, 0 to 79%,
• 0 to 20 kPa (at 760 mmHg)
• Accuracy: ± 2mm Hg (0-40mmHg)
• ± 5% of reading (41-70 mmHg)
• ± 8% of reading (71-100 mmHg)
• ± 10% of reading (101-150 mmHg)
Frequency: 0-120 rpm
Accuracy:
• ± 2rpm (0-70rpm)
• ± 5 rpm (> 70 rpm)
Response time: <240 ms (10% to 90%)
Delay time: <2s

C02 COMEN Main Flow
Range: 0 to 150 mm Hg, 0 to 79%,
0 to 20 kPa (at 760 mmHg)

Accuracy: ± 2mmHg (0-40mmHg)
• ± 5% of reading (41-70 mmHg)
• ± 8% of reading (71-100 mmHg)
• ± 10% of reading (101-150 mmHg)
Frequency: 0-120 rpm
Accuracy:
• ± 2rpm (0-70rpm)
• ± 5 rpm (> 70 rpm)
Delay time: <2s

The images shown are for illustrative purposes only and may differ from the actual product. Specifications are subject to change without notice.
Syringe Infusion Pump Model SN-50T66, three channels, standard support
GENERAL CHARACTERISTICS
* It is characterized by its high precision, stable flow rate and low dosage. It is particularly used for the infusion of sodium nitroprusside, dopamine, propofol and antibiotics for acute and severe diseases.
* The equipment can store personalized syringe information from 33 different manufacturers, Weigao and 32 other manufacturers, configurable by the user.
* The SN-50F66 pump can use sterile and disposable syringes of 5ml, 10ml, 20ml, 30ml or 50ml. It Automatically recognices the placed syringe.
* The equipment can store up to 2000 historical infusion records, which include the following information: injection mode, injection rate, alarm information, total volume injected, threshold value of the line of occlusion pressure limit, limiting quantity, number of syringe and operation information.
* It has the following alarm functions:
Incorrect position of the syringe.
Residual Limit
Occlusion
End of injection.
No operation
Empty syringe.
Flow limit exceeded.
Plunger decoupled.
Power cord disconnected.
Battery discharged.
Battery exhausted
System error
* Battery operating time: starting from a full charge, the battery can withstand 5 hours of operation at a speed of 5 ml / h on two channels.
* Allows operation and battery charging from the 12V connector of the car.

TECHNICAL SPECIFICATIONS
Dimensions: (Length x Width x Height)
3-channel pump: 469mm x 277mm x 207mm
Weight:
3-channel pump: 5.4kg (includes support).
Feeding:
AC input: 100V ~ to 240V ~, 50/60 Hz.
DC input: 12Vdc
Battery voltage: 12Vdc
Nominal power: 40 VA.
Quality Standards: ISO13485, Disp. A.N.M.A.T. 3266/2013: B.P.F. and Disp. A.N.M.A.T. 2319/02; certified.
Safety Standards: UNE-EN 60601-1. (Eq. IRAM 4220-1 and IEC 601-1), Class I - Prot. Desc. Elect .: CF, UNE-EN 60601-1-2 (Electromagnetic Compatibility).
Authorized by A.N.M.A.T .: PM 1125-18.

ACCESSORIES
● 1 Power cable.
● 1 User manual.
● 1 List of content.
● 1 Certificate of manufacturing quality.
● 1 Warranty card.

The images shown are for illustrative purposes only and may differ from the actual product. Specifications are subject to change without notice.
Defibrillator Monitor 3850B Monophasic Feas Electrónica
The model 3850B Monophasic from FEAS ELECTRÓNICA is a monophasic waveform external defibrillator monitor up to 360J, selectable in steps, which allows defibrillation in asynchronous mode or synchronized with the R wave of the patient's ECG for the application of synchronized cardioversion.

It allows the monitoring and surveillance of ECG, with heart rate measurement, through the paddles, or cable to patient with 3 lead or 5 lead.

In addition, optionally, you can monitor pulse oximetry, graphing the plethysmographic curve on the screen and a pulse width indicator bar, indicating the SpO2 and pulse rate values. Both ECG and SpO2 monitoring allow the setting of alarms that allow monitoring of heart rate, SpO2 value and pulse rate.

It is of the portable type, powered by an internal rechargeable battery, a 90 Vac - 240 Vac, 50 Hz or 60 Hz mains supply or an external 12 Vdc source.
Optionally, it has a transcutaneous pacemaker that allows temporary electrical stimulation to the patient in a non-invasive way, in fixed mode (asynchronous) or on demand (synchronous), using electrodes.

Optionally, you can also have a thermal recorder for real-time recording of up to two curves, an ECG lead, and, optionally, the plethysmographic curve, manually when the operator decides or automatically during charging.

MONITOR
• Electrocardiogram monitor with LCD screen.
• Electrocardiogram signal acquired by cable to patient or by paddles.
• Derivations:
- With 3-lead cable: DI, DII, DIII and PAL.
- With 5-lead cable: DI, DII, DIII, aVR, aVF, aVL, precordial and PAL.
• Cascade electrocardiogram.
• Digital heart rate indicator.
• Low battery indicator.
• Battery charging indicator light.
• Alarm silence key.
• Heart rate alarms from 20 [beats / min] to 250 [beats / min].
• ECG gain: 1/6, 1/4, 1/2, 1 and 2 cm / mV.
• Equipment suitable for hospital use.

DEFIBRILLATOR
• Monophasic wave
• Use of the Defibrillator in three steps:
1- Power on and energy selection.
2- Loading.
3- Triggering of energy by means of pushbuttons on paddles or from keyboard.
• Charge selection key in steps: 2, 3, 5, 7, 10, 20, 50, 100, 200, 300 and 360 Joules.
• Auditory and visual indication of end of charge.
• Indication of stored energy on display.
• Triggering energy by simultaneously pressing both paddle pushbuttons or the “SCHOCK” key.
• The internal charge cancellation occurs when the "DISARM" key is pressed or when 60 seconds have elapsed from the end of the energy charge or when the energy selector switch is turned to the "MONITOR" or "OFF" position. Energy is discharged internally without being present in paddles.
• Direct or synchronized discharge.
• Auditory and visual indication of synchronous mode.
• Discharge capacity: 80 discharges at maximum energy, with the internal battery fully charged.
• Charging time at 360 J: less than 6 seconds.
• Connection to internal paddles or defibrillation pads.
• The equipment has a delivered energy test.

TRANSCUTANEOUS PACEMAKER (OPTIONAL)
• External stimulation through electrodes.
• Frequency: 40 ppm to 180 ppm (selectable in steps of 5 ppm).
• Current: 10 mA to 200 mA (selectable in steps of 5 mA).
• Mode: Selectable, on demand or fixed.
• Pulse width: 20 ms ± 5%.
Accessories included:
Elastic belt for external Pacemaker electrode.
Pacemaker lead cable.
Pair of gray electrodes.

OXYGEN SATURATION (SpO2) (OPTIONAL)
SpO2 measurement:
• Range: 0% to 100%.
• Accuracy:
Adult: ± 2% between 70% and 100%.
Neonatal: ± 3% between 70% and 100%.
In motion: ± 3% between 70% and 100%.
• Resolution: 1%.
• Percent oxygen saturation alarm
Upper limit: 1 to 100.
Lower limit: 0 to 99.
• Measurement of pulse rate and alarms from 30 to 250 [1 / min] ± 3 [1 / min] and ± 5 [1 / min] in motion.
• Resolution: 1 [1 / min].
Accessories included:
Oximetry Sensor Extender
Choice of adult or pediatric, clip-on or disposable oximetry sensor.

REGISTER (OPTIONAL)
• Direct registration key.
• Automatic registration when the power charge process starts up to 20 seconds after pressing the Shock key.
• High resolution thermal recorder.
• Registration speed: 25 mm / s.
• Prints: date and time, energy in Joules, EKG curve, Gain, Heart rate, Lead, Sweep speed, Plethysmographic curve, SpO2, Pulse rate, Mode, Pacemaker rate, Pacemaker current.
• Paper: width of 50 mm and maximum diameter of 45 mm.
Accessory Included:
50 millimeter roll of paper.

TECHNICAL SPECIFICATIONS
• Supply voltage: 90Vac to 240Vac - 50/60 Hz or 12 Vdc.
• Internal rechargeable NiMh battery - 12V, 3500 mAh.
• Consumption 180 W (7W during standby).
• Size: 295mm (width) x 200mm (height) x 345mm (length).
• Weight: 6 kg (including external paddles, battery and recorder).

CERTIFICATIONS
• Quality standards:
- ISO13485 (certified).
- Disp. A.N.M.A.T. 3266/2013: B.P.F.
- Disp. A.N.M.A.T. 2319/02.

• Safety rules:
- EN 60601-1 (Eq. IRAM 4220-1 and IEC 601-1).
- EN 60601-1-2 (Electromagnetic Compatibility).
- EN 60601-1-6.
- EN 60601-1-8.
- EN 60601-2-4.
- EN 60601-2-27.
- EN 60601-2-49.
- ISO 80601-2-61.
Authorized by the A.N.M.A.T. PM-1125-4.

ACCESSORIES INCLUDED
External paddle set for adults.
Power cable for external +12 Vdc input.
Line power cable.
Patient cable with 3 or 5 wires for ECG.
10 disposable electrodes.
User manual.

The images shown are for illustrative purposes only and may differ from the actual product. Specifications are subject to change without notice.
Defibrillator Monitor 3850B Monophasic for simulation, Feas Electrónica
Simulation defibrillator. DOES NOT DISCHARGE ENERGY.

The Model 3850B Monophasic from Feas Electronica is an external defibrillator monitor with a monophasic waveform up to 360 J, selectable in steps.
It allows the monitoring and surveillance of ECG, with heart rate measurement, through the paddles, or cable to patient with 3 lead or 5 lead.

In addition, optionally, you can monitor pulse oximetry, graphing the plethysmographic curve on the screen and a pulse width indicator bar, indicating the SpO2 and pulse rate values. Both ECG and SpO2 monitoring allow the setting of alarms that allow you to monitor your heart rate, SpO2 value, and pulse rate.

It is of the portable type, powered by an internal rechargeable battery, a 90 Vac - 240 Vac, 50 Hz or 60 Hz mains supply or an external 12 Vdc source.
Optionally, it has a transcutaneous pacemaker that allows temporary electrical stimulation to the patient in a non-invasive way, in fixed mode (asynchronous) or on demand (synchronous), using electrodes.

Optionally, you can also have a thermal recorder for real-time recording of up to two curves, an ECG lead, and, optionally, the plethysmographic curve, manually when the operator decides or automatically during charging.


FEATURES
MONITOR
• Electrocardiogram monitor with LCD screen.
• Electrocardiogram signal acquired by cable to patient or by paddles.
• Derivations:
With 3-lead cable: DI, DII, DIII and PAL.
With 5-lead cable: DI, DII, DIII, aVR, aVF, aVL, Precordial and PAL.
• Cascade electrocardiogram.
• Digital indication of heart rate.
• Low battery indicator.
• Battery charging indicator light.
• Alarm silence key.
• Heart rate alarms from 20 [1 / min] to 250 [1 / min].
• ECG gain: 1/6, 1 / 4.1 / 2, 1 and 2 [cm / mV].

DEFIBRILLATOR
• Use of the Defibrillator in three steps:
1. Power on and power selection.
2. Loading.
3. Triggering of energy by means of push buttons on paddles or from keyboard.
• Step load selection key: 2, 3, 5, 7, 10, 20, 50,100, 200, 300 and 360 [Joules].
• Auditory and visual indication of end of charge.
• Indication on display of stored energy.
• Energy Trigger by simultaneously pressing both paddle pushbuttons or the “SHOCK”key.
• Internal charge cancellation:
It occurs when the "DISARM" key is pressed or when 60 seconds have elapsed from the end of the energy charge or when the energy selector switch is turned to the "MONITOR" or "OFF" position.
• It does not perform downloads but can, for simulation, be configured as direct or synchronized.
• Auditory and visual indication of synchronous mode.

REGISTER (OPTIONAL)
• Direct registration key.
• Automatic registration when the power charge process starts up to 20 seconds after pressing the Shock key.
• High resolution thermal recorder.
• Registration speed: 25 mm / s.
• Prints: Date and Time, Energy in Joules, EKC Curve, Gain, Heart Rate, Lead, Sweep Rate, Plethysmographic Curve, SpO2, Pulse Rate, Mode, Pacemaker Rate, Pacemaker Current.
• Paper: 50mm width, 45mm maximum diameter.
Accessory Included:
50 millimeter roll of paper.

TRANSCUTANEOUS PACEMAKER (OPTIONAL)
• External stimulation through electrodes.
• Frequency: 40 ppm to 180 ppm. (Selectable in steps of 5 ppm).
• Current: 10 mA to 200 mA. (Selectable in steps of 5 mA).
• Mode: Selectable, on demand or fixed.
• Pulse width: 20 ms ± 5%.
Accessories included:
Elastic belt for external Pacemaker electrode.
Pacemaker lead cable.
Pair of gray electrodes.

OXYGEN SATURATION (SpO2) (OPTIONAL)
SpO2 measurement:
• Range 0% to 100%.
• Accuracy:
Adult ± 2% between 70% and 100%.
Neonatal ± 3% between 70% and 100%.
In Motion ± 3% between 70% and 100%.
• Resolution: 1%.
• Percent oxygen saturation alarm:
Upper limit: 1 to 100.
Lower limit: 0 to 99.
• Measurement of pulse rate and alarms from 30 to 250 [1 / min] ± 3 [1 / min] and ± 5 [1 / min] in Motion.
• Resolution: 1 [1 / min].
Accessories included:
Oximetry Sensor Extender
Choice of adult or pediatric, clip-on or disposable oximetry sensor.

TECHNICAL SPECIFICATIONS
• Supply voltage: 90 Vac to 240 Vac - 50 Hz / 60 Hz, or 12 Vdc.
• Internal rechargeable NiMh battery - 12 V, 3500 mAh.
• Consumption: 10 W.
• Size: 295mm (width) x 200mm (height) x 345mm (depth).
• Weight: 5 Kg (Including external paddles, battery and recorder).

The images shown are for illustrative purposes only and may differ from the actual product. Specifications are subject to change without notice.
Syringe infusion pump model SN-50C66T: one channel, standard support, with weight mode
Syringe infusion pump model SN-50C66T is a constant volume, channel and speed controlled infusion pump. It is characterized by high precision, stable flow rate and low dosage.

It is used particularly for the infusion of sodium nitroprusside, dopamine, propofol and antibiotics for acute and serious illnesses. The pump has multiple types of alarm functions to ensure a safe and reliable infusion process.

This product is used to clinically control the flow and velocity of fluids (drugs, nutrients, and blood) infused into the patient's body for safer use.

GENERAL CHARACTERISTICS
* The equipment can store customized syringe information from 33 different manufacturers, Weigao and 32 other manufacturers, configurable by the user.
* SN-50C66T pump can use sterile and disposable syringes of 5ml, 10ml, 20ml, 30ml or 50ml. Automatically recognizes the syringe in place.
* The equipment can store up to 2000 historical infusion records, which include the following information: injection mode, injection rate, alarm information, total volume injected, threshold value of the occlusion pressure limit of the path, limiting quantity, number of syringe and information of the operation.
* It has the following alarm functions:
Incorrect position of the syringe.
Residual limit.
Occlusion.
End of injection.
No operation.
From empty syringe.
Flow limit exceeded.
Plunger decoupled.
Power cord disconnected.
Discharged battery.
Dead battery.
System error.
* Battery operating time: starting from a full charge, the battery can support 6 hours of operation on one channel at a rate of 5 ml / h.
* Allows operation and battery charging from the car's 12Vdc connector.
* Intended User: Adult, Pediatric, Neonatal

TECHNICAL SPECIFICATIONS
* Dimensions:
306mm x 140mm x 146mm (Length x Width x Height)
* Weight: 2.25kg (includes support).
* Electrical feeding:
AC input: 100V to 240V, 50/60 Hz.
DC input: 12Vdc.
Battery voltage: 12Vdc.
Nominal power: 40 VA.

CERTIFICATES:
* Quality standards:
ISO13485
Disp. A.N.M.A.T. 3266/2013: B.P.F.
Disp. A.N.M.A.T. 2319/02
* Safety rules:
UNE-EN 60601-1. (Eq. IRAM 4220-1 and IEC 601-1), Class I - Prot. Desc. Elect .: CF
UNE-EN 60601-1-2 (Electromagnetic Compatibility).
Authorized by the A.N.M.A.T .: PM 1125-18.

The images shown are for illustrative purposes only and may differ from the actual product. Specifications are subject to change without notice.
Patient Monitor, Multiparameter, of 12,1", Comen, with Batery Li ion include, Touch screen, light, model C80
MULTIPARAMETER MONITOR C80

C80 provides the clinician with advanced functionality and monitoring options to meet the demands of a wide range of care in any hospital setting.
It has a color screen with TFT technology of 10.4" inclined to facilitate observation.
Easy menu use via rotary knob and touch screen.
In addition, it has reserved expansion ports such as for SD card, USB port and network.

Adult, Pediatric, Neonatal Use

ELECTROCARDIOGRAM(ECG)
Heart rate:
•Adult: 15-300 [1/min]
•Neonates/children: 15 - 350 [1/min]
Accuracy: ±1% o ±1 [1/min], whichever is greater.
Resolution: ±1 [1/min]
Gain selection: 1.25mm/mV, 2.5mm/mV, 5.0mm/mV, 10mm/mV, 40mm/mV, Auto.
Manual replacement.
Automatic selection of cable to patient.
3, 5, 12 lead ECG input mode.
Selection of leads:
1. DI, DII, DIII
2. DI, DII, DIII, aVR, aVL, aVF y V
3. DI, DII, DIII, aVR, aVL, aVF y V1 a V6
Frequency response:
•Monitoring mode: 0.5-40Hz.
•Deagnostic mode: 0.05-130Hz.
•Surgery modality: 1-20Hz.
•ST Mode: 0.05-40hZ.
Heart rate alarms:
•Adult: 15 - 300 [1/min]
•Neonates/children: 15 - 350 [1/min]
Loose electrode detection.
Pacemaker Pulse Suppression Capability:
Amplitude of ±2mV~±700mV and pulse width of 0.1ms - 2.0ms.

ANALYSIS AND CLASSIFICATION OF ARRHYTHMIAS
Arrhythmia type: PVC, Asystoloe, VTac, Tachycardia, Ventricular tachycardia, Supraventricular tachycardia, VR, Bigeminia, Trigeminia, R on T, Bradycardia, Ventricular bradycardia, missed beats, Atrial fibrillation, Ventricular fibrillation, Non-captured pacemaker (NCP), Non-captured pacemaker (PNP).
ST segment analysis:
Range: -2mV to +2mV
Accuracy: Measurement tolerance within (-0.8 mV)-(+0.8 mV) is ±0.02 mV or ±10%, whichever is greater. It is not defined for other ranges.
Resolution: 0.01mV (0.1mm)

OXYGEN SATURATION
Plethysmographic curse, arterial oxygen saturation (SpO2) values, peripheral pulse rate (FFPP) and pulse intensity bar.
Comen SpO2:
Range: 0% - 100%
Adult/Child Accuracy: Within 70% -100%, the tolerance is ±2% (without movement).
Neonatal Accuracy: within 70% -100%, the tolerance is ±3% (no movement).
Resolution: 1%
Alarm: 0% to 100%

PULSE RATE
Comen SpO2:
Range: 20 - 254 [1/min]
Resolution: 1[1/min]
Accuracy: ±2 [1/min]
Alarm: 20 a 350 [1/min]

RESPIRATORY CURVE
Impedance method.
Breathing frequency:
•Monitoring range for adult: 0 to 120 [1/min]
•Monitoring range for child/neonate: 0 to 150 [1/min]
Within 7 [1/min] – 150 [1/min], the measurement error is ±2 rpm or ±2%, whichever is greater.
The tolerance is not defined by other ranges.
Alarm Limit Specification:
•Monitoring range for adult: 0 to 120 [1/min]
•Monitoring range for child/neonate: 0 to 150 [1/min]
Apnea alarm

NON-INVASIVE PRESSURE
Automatic Oscillometric Method
Measurement mode: Manual, auto (cyclical) or continuous (not suitable for neonates)
Measurement unit: mmHg
Nominal Monitoring Range:
•Adult Range: Systolic: 40 – 270 mmHg,
Diastolic: 10 – 215 mmHg,
Average: 20 – 235 mmHg
•Pediatric range: Systolic: 40 – 200 mmHg,
Diastolic: 10 – 150 mmHg,
Average: 20 – 165 mmHg
•Neonatal Range: Systolic: 40 – 135 mmHg,
Diastolic: 10 – 100 mmHg,
Average: 20 – 110 mmHg
Alarm Limit Specifications:
•Adult Range: Systolic: 40 – 270 mmHg,
Diastolic: 10 – 215 mmHg,
Average: 20 – 235 mmHg
•Pediatric Range: Systolic: 40 – 200 mmHg,
Diastolic: 10 – 150 mmHg,
Average: 20 – 165 mmHg
•Neonatal Range: Systolic: 40 – 135 mmHg,
Diastolic: 10 – 100 mmHg,
Average: 20 – 110 mmHg
Precision:
The mean error should be less than 5mmHg
The standard deviation should be less than 8mmHg.
Manual or automatic start of measurement at programmable intervals of 1/ 2/ 2.5/ 3/ 4/ 5/ 10/ 15/ 30/ 60/ 90/ 120/ 180/ 240/ 480/ 720min.
Measurement time under continuous mode: 5 min
Overpressure protection:
•Adult: When the cuff pressure exceeds 297 mmHg ±3mmHg, the control valve will relieve the pressure.
•Child: When the cuff pressure exceeds 240 mmHg ±3 mmHg, the control valve will relieve the pressure.
•Neonate: When the cuff pressure exceeds 147 mmHg ±3mmHg, the control valve will relieve the pressure.
Resolution: 1 mmHg.

TEMPERATURE
Measurement Method: direct.
A temperature channel.
Temperature Ranges
Range: 0 - 50° C
Accuracy: ±0.1°C (Exclusive of probe tolerance)
Resolution: 0.1°C
Maximum and minimum temperature alarms:
Range: 0 - 50° C


TECHNICAL SPECIFICATIONS

12.1" color touch screen with TFT technology Resolution: 800 X 600
Inclined screen to facilitate observation.
Dimensions: 344 mm x 291 mm x 165 mm
Weight 3.9 Kg. with battery
Power supply: It has an internal battery and an external AC.
Supply voltage:
100 – 240 Vac, 50/60 Hz.
C80: Standard: Li-Ion 11.8V/2200mAh.
Once fully charged, it ensures continuous autonomous operation for 2 consecutive hours.
Consumption: 60VA
Reserved expansion ports such as SD card, USB port and network.
Quality standards:
IEC 60601-1, IEC 60601-1-8, IEC 60601-2-27, EN 1060-3, IEC 80601-2-30, IEC60601-2-34, IEC60601-2-49, ISO 80601-2-56, ISO 80601-2-61, Class 1, IPX1.

The images shown are for illustrative purposes only and may differ from the actual product. Specifications are subject to change without notice.
Patient Monitor, Multiparameter, Modular, Comen, Model C90 + C30
COMEN C90 is a device designed to meet the most advanced needs for room monitoring, intermediate care, intensive care, among others. Created to be used in adult, pediatric and neonatal patients. Able to improve in its benefits, according to the needs of the user and the complexity of its clinical unit. This is due to the use of modules for the different extended functions that are required by clinicians.
Features
• It has a C30 multiparameter module, removable and usable as transfer equipment.
• Large high resolution touch screen
• For highly complex monitoring

OTHER PRODUCT NAMES
Multi-Parameter Monitor / Patient Monitor / Vital Signs Monitor / Cardiomonitor

FREQUENT QUESTIONS
Can it be used on animals?
Yes, please let us know when buying and we will make the adaptation of the accessories.

The images shown are for illustrative purposes only and may differ from the actual product. Specifications are subject to change without notice.