Biphasic 3850B defibrillator monitor
331,638.13 331,638.13 331638.13 ARS
FEATURES
MONITOR
Electrocardiogram monitor with LCD screen.
Electrocardiogram signal acquired through 3 or 5 leads patient cable or through paddles.
Leads selection:
- With 3 leads cable: DI, DII, DIII and PAL.
- With 5 leads 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
Direct access key for record command.
Automatic recording if occurs an event.
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, Diameter Max: 45 mm.


OXYGEN SATURATION
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''100. Lower limit: 0''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].

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 with coil cable.
Power cable for external +12 power supply.
AC Power cord.
3 or 5 leads cable for patient for ECG.Disposable electrodes.
User's manual.

The image is illustrative.
LCD Multiparameter Patient Monitor
175,294.44 175,294.44 175294.44 ARS
GENERAL CHARACTERISTICS
FEATURES:
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 CHANNELSELECTROCARDIOGRAM
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 leads patient cable. Lead selection: DI, DII or DIII.
12 leads with 5 leads 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 and 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.

SIDESTREAM CAPNOGRAPHY 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 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.

FiO2Fraction of inspired Oxygen: from 0% to 100%.
Polarographic cell measurement principle.
Alarms minimum and maximum: 0% to 100% and off.

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

TECHNICHAL SPECIFICATIONS15” LCD-TFT Color Monitor Resolution: 1024x768.
Greater angle of view.
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.
Enteral nutrition pump model SN-600N Sino MDT Ltd
140,072.63 140,072.63 140072.63 ARS
Enteral nutrition pump, easy to use, suitable for the infusion of clinical enteral nutrients for example: patients with afagia.
• Convenient:
Transparent pump door, allows visibility of the infusion process.
It operates silently and without vibrations thanks to its high quality motor.
Visual and auditory alarms.
Rinse function of the infusion set.
Con fi guration of infusion time.
• Compact:
Elegant design of the flow line.
Light weight: 1.3 kg.
Easy to transport
• Safe:
Display of the operating status through its indicator.
Programmable fl ow speed and preset volume.
Its design provides an effective prevention against the entry of liquids.
High definition screen, which allows to visualize the main configuration of the infusion process.
Detection of the number of bubbles.
• Smart:
Intermittent feeding output, allowing to establish a period of pause so that the patient can swallow quietly.
It has two modes of operation: Continuous mode and pulse mode.
Stores 1500 historical records.
USB connection
Indication of the status of the power supply.
TECHNICAL SPECIFICATIONS
Flow rate: 1 ml / h ~ 600 ml / h. Preset volume: 0 ml ~ 9999 ml. Total amount accumulated: 1 ml ~ 9999 ml. Accuracy: ± 5%.
Bolus fl ow velocity: 3 adjustable levels: 200 ml / h, 400 ml / h, 600 ml / h.
Automatic Calibration: This unique design can automatically adjust flow accuracy for different viscosity nutrition solutions.
Occlusion pressure range: 500 ± 200 mmHg. Alarm volume: 3 levels.
Keyboard sound: The sound of the key has 3 different levels or it can be muted.
Historical record: Up to 1500 historical records can be stored.
Supply voltage: 110 V ~ A 240 V ~ - 50 Hz or 60 Hz Built-in battery: Ni-Mh, 12 Vdc, 800 mAh.
Operating time: with the battery fully charged, it can run continuously for 5 hours at a speed of 25 ml / h. Power consumption: 11 VA.
Environmental operating conditions:
- Ambient temperature: - 5 ºC to + 40 ºC.
- Ambient humidity: 20% to 90%.
- Environmental pressure: 76.0 kPa to 106.0 kPa. Protection against the entry of liquids: IPX4. Dimensions: 146 mm x 199.5 mm x 114 mm. Weight: 1.3 kg (with hanging support).
Protection against electric shock: Type I, class CF.
ACCESSORIES INCLUDED
- Power cord.
- User's manual.
- Certi fi cate of quality.
- Warranty card.
Feas Electrónica's Automatic External Defibrillator (AED), model: Heart+ ResQ NT-381.C
166,012.00 166,012.00 166012.0 ARS
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 2015 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 @ 25 ºC.
• Capacity: 180 shocks @ 25 ºC, 130 shocks @ 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.
Infusion pump model SN-1500H, Sino MDT Ltd.
140,072.63 140,072.63 140072.63 ARS
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 four types of infusion mode: Speed ​​mode, Drip mode, Body Weight mode and Time 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).
Infusion pump model SN-1800V, Sino MDT Ltd.
129,696.88 129,696.88 129696.88 ARS
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 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 five types of infusion mode: Speed mode, Drip mode, Body Weight mode, Time mode and Infusion Plan.
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-1500H: 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).
Infrared Thermometer NewTop, model HRX-T1803
4,150.30 4,150.30 4150.3 ARS
TERMÓMETRO INFRARROJO PARA MEDICIÓN SIN CONTACTO.
- Termómetro digital de frente con tecnología infrarroja sin necesidad de contacto.
- Fácil de usar. Medí la temperatura de forma simple y rápida con solo presionar un botón. El tiempo de medición es de sólo 1 segundo.
- Posee alerta de fiebre sonora (>= 37.8ºC).
- Ideal para medir la temperatura en adultos, niños y bebés. También puede medir la temperatura en superficies de objetos y líquidos. El rango de medición en personas es de 32ºC a 42.9ºC y el rango en superficies es de 0ºC a 100ºC.
- Medición precisa. Ideal para tomar la temperatura corporal con margen de error mínimo (+- 0,2º).
- Pantalla LCD iluminada en tres colores: verde, naranja y rojo.
- Seguro e higiénico. Ideal para uso doméstico y profesional.
- Capacidad para guardar en su memoria hasta 32 lecturas.
- Apagado automático a los 15 segundos.

CARACTERÍSTICAS TÉCNICAS:
Nombre: Termómetro infrarrojo.
Modelo: HRX-T1803
Medición sin contacto.
Distancia de medición: 3-15cm.
Rango de medición: 32-42.5ºC (89.6-108.5ºF)
Precisión:
- 35-42ºC +- 0.2ºC
- 35-42º +- 0.3ºC
Unidad de medición: ºC/ºF
Apagado automático: 15 segundos.
Peso: 142 gr.
Dimensiones: 170*95*45mm
Emergency trolley CP 2000
140,072.63 140,072.63 140072.63 ARS
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.
Odontology implant system
150,658.46 150,658.46 150658.46 ARS
· 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.

















Multi uses trolley Mod. CT62512D Feas Electrónica
78,855.70 78,855.70 78855.7 ARS
Carro de usos múltiples con dos estantes y cajón divisible.
Electrophysiology and hemodynamic polygraph system mod. 1405
0.00 -0.0 ARS
CARACTERÍSTICAS

ELECTROFISIOLOGÍA
- 18 canales endocavitatorios simultáneos.
- Calibres en Pantalla (Calipers): permiten medir tiempo entre eventos de interés.
12 derivaciones simultáneas de ECG de superficie.
- Hasta 4 Presiones Invasivas.
- Presentación tabular de mediciones de P.N.I.
- Pantalla Dividida (Split): que permite tener una imagen de referencia congelada en una ventana, y en la otra ver el monitoreo a tiempo real.
- Acceso rápido a la ventana de configuración de curvas, donde puede realizar una selección continua de posición, amplitud, selección de filtros y personalizar colores y etiquetas de curvas.
- Disparo sincronizado del barrido de curvas (trigger).
- Grabación de Estudios en disco rígido, para transportarlos a otros equipos u ordenadores personales mediante pen drive.
- Un canal de SpO2.
- Impresión de estudios con selección de color y ancho de trazo.
- Caja de conexión de Catéteres y Estimulador Cardíaco.
- Revisión de estudios grabados, con posibilidad de modificar la ganancia, posición, color y límites (de amplitud) de las curvas.
- Teclas de acceso rápido.

HEMODINAMIA
- 2 Derivaciones de ECG simultáneas en pantalla, seleccionables entre 12 derivaciones utilizando cables de 10 electrodos.
- Hasta 4 Presiones Invasivas.
- Cálculo automático de la reserva fraccional de flujo (FFR) en tiempo real, sin necesidad de contar con un analizador de FFR independiente (externo). La FFR permite determinar la severidad hemodinámica de las lesiones vasculares.
Visualización numérica y gráfica del valor de FFR.
Almacenamiento del estudio.
- Gasto cardíaco por termodilución. Cálculo de BSA, CO, CI, SV, SI.
Selección de la constante de cómputo k del catéter.
Selección del volumen de inyectado.
Ingreso de datos del paciente (altura y peso).
Medición de la temperatura de la sangre y del inyectado.
Curva de la variación de temperatura de la sangre.
Mensajes en pantalla.
- Grabación de estudios, almacena curvas y cálculos.
- Medición de la temperatura corporal o del inyectado (durante el gasto cardíaco).
- Permite congelar curvas y medir tiempos y amplitudes mediante calibres.
- Impresión de curvas congeladas o de estudios grabados.
- CÁLCULOS HEMODINÁMICOS:
- Área valvular aórtica.
- Área valvular pulmonar.
- Cálculo de las Resistencias vascular pulmonar y sistémica.

OPCIONALES
Oximetría de Pulso
Curva pletismográfica, visualización de la saturación porcentual de oxígeno.
Medición de señal de baja perfusión y con movimiento.
SpO2: Rango desde 0% a 100%.
Precisión Adulto: 2% de 70% a 100%.
Precisión Neonatal: 3% de 70% a 100%.
Precisión en movimiento: 3% de 70% a 100%.
Resolución: 1%.
Frecuencia de Pulso: Rango desde 20 [1/min] a 300 [1/min].
Precisión Adulto: ±3 [1/min].
Precisión Neonatal: ±3 [1/min].
Precisión en movimiento: ± 5 [1/min].
Resolución: 1 [1/min].

Presión No Invasiva
Inicio de la medición en forma manual o automática a intervalos programables desde 2 minutos a 90 minutos.
Selección de paciente Adulto o Neonatal.
Visualización de las últimas 1440 mediciones.
Impresión de las mediciones en forma tabular.
Incluye cuff (manguito).

ESPECIFICACIONES TÉCNICAS
Display: Monitor LCD 19”
- Dimensiones: 19” (mayor tamaño; opcional)
- Resolución: 1024 x 768 puntos
CPU: - Placa madre de PC Industrial.
- Disco rígido de 160 Gb.
- Salida para conectar un monitor remoto adicional.
Impresora: - Tecnología Láser.
- Resolución 1200 dpi.
Alimentación: - 110V~ / 220V~.
- Frecuencia 50/60 Hz.
Norma de Calidad: ISO9001 (certificado).
ISO13485 (certificado).
Disp. A.N.M.A.T. 3266/2013: B.P.F. (certificado).
Disp. A.N.M.A.T. 2319/02 (certificado).
Norma de Seguridad: UNE-EN60601-1(Eq. IRAM 4220-1 e IEC 60601-1) Clase I.
Protección contra descargas eléctricas: CF.
Autorizado por la A.N.M.A.T. PM 1125-23.

ACCESORIOS INCLUIDOS
- Preamplificador para Estudios Hemodinámicos.
- Cable de interconexión de CPU a Preamplificador.
- Monitor, teclado y mouse.
- Cable "Y" Minidin-M a 2 Minidin-F.
- Impresora.
- Pedal de grabación con cable.
- Cables de alimentación de CPU, monitor e impresora.
- Cable de datos a impresora.
- Cable a tierra para interconexión entre CPU y Preamplificador.
- Soporte metálico para Preamplificador.
- Caja prolongadora de catéter.
- Cable de interconexión para caja prolongadora de catéter.
- Porta equipos mini.
- TMM Abrazadera de montaje de soporte para TBC.
- Placa soporte para 4 transductores.
- Zapatilla de 5 tomas.
- Electrodos descartables.
- 4 transductores de presión descartables.
- 4 cables de interconexión de Preamplificador a transductores de presión descartables.
- Caja derivadora de parámetros de Presión Invasiva.
- Sensor de temperatura de inyectado.
- Cable a paciente de 3, 5 o 10 broches.
- Cable adaptador a catéter de gasto cardíaco.
- Sensor de Oxímetro.
- Cable prolongador de Oxímetro.
- Cuff Reus Adulto.
- Manguera de silicona para PNI, 3m.
- Adaptador digital para guías de presión (FFR).
- Cable adaptador de guía de presión Volcano (FFR).
- Carro de transporte (opcional).
- Manual de uso.
PACE 101 single chamber cardiac pacemaker OSYPKA
259,393.75 259,393.75 259393.75 ARS
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
C50 Multi-parameter patient monitor Comen
234,515.53 234,515.53 234515.53 ARS
MONITOR MULTIPARAMÉTRICO C50

C50 brinda al médico opciones de monitoreo y funcionalidades avanzadas con el objetivo de cumplir con las demandas de un amplio rango de cuidados en cualquier entorno hospitalario.
Posee una pantalla a color con tecnología TFT de 10.4"" inclinada para facilitar la observación.
Uso fácil del menú mediante mando giratorio y pantalla táctil.
Además, cuenta con puertos de expansión reservados como por ejemplo para tarjeta SD, puerto USB y red.

Uso Adulto, Pediátrico, Neonatal

ELECTROCARDIOGRAMA (ECG)
Frecuencia cardíaca:
•Adulto: 15-300 [1/min]
•Neonatos/niños: 15 - 350 [1/min]
Precisión: ±1% o ±1 [1/min], el que sea mayor.
Resolución: ±1 [1/min]
Selección de ganancia: 1.25mm/mV, 2.5mm/mV, 5.0mm/mV, 10mm/mV, 40mm/mV, Auto.
Reemplazo manual.
Selección automática de cable a paciente.
Modalidad de entrada ECG de 3, 5, 12 derivaciones.
Selección de derivación:
1. DI, DII, DIII
2. DI, DII, DIII, aVR, aVL, aVF y V
3. DI, DII, DIII, aVR, aVL, aVF y V1 a V6
Respuesta de frecuencia:
•Modalidad monitoreo: 0.5-40Hz.
•Modo diagnóstico: 0.05-130Hz.
•Modalidad cirugía: 1-20Hz.
•Modalidad ST: 0.05-40hZ.
Alarmas de frecuencia cardíaca:
•Adulto: 15 - 300 [1/min]
•Neonatos/niños: 15 - 350 [1/min]
Detección de electrodo suelto.
Capacidad de supresión de pulso de marcapasos:
Amplitud de ±2mV~±700mV y ancho de pulso de 0.1ms - 2.0ms.

ANÁLISIS Y CLASIFICACIÓN DE ARRITMIAS
Tipo de arritmia: PVC, Asístole, VTac, Taquicardia, Taquicardia ventricular, Taquicardia supra ventricular, VR, Bigeminia, Trigeminia, R sobre T, Bradicardia, Bradicardia ventricular, latidos perdidos, Fibrilación atrial, Fibrilación ventricular, Marcapasos no capturado (PNC), marcapasos no marca (PNP).
Análisis del segmento ST:
Rango: -2mV a +2mV
Precisión: Tolerancia de medición dentro de (-0.8 mV)-(+0.8 mV) es ±0.02 mV o ±10%, cualquiera sea superior. No está definido para otros rangos.
Resolución: 0.01mV (0.1mm)

SATURACIÓN DE OXÍGENO
Curva pletismográfica, valores de saturación de oxígeno arterial (SpO2), frecuencia de pulso periférico (FFPP) y barra de intensidad del pulso.
Comen SpO2:
Rango: 0% - 100%
Precisión adulto/niño: Dentro del 70% -100%, la tolerancia es ±2% (sin movimiento).
Precisión neonatal: Dentro del 70% -100%, la tolerancia es ±3% (sin movimiento).
Resolución: 1%
Alarma: 0% a 100%

FRECUENCIA DE PULSO
Comen SpO2:
Rango: 20 - 254 [1/min]
Resolución: 1[1/min]
Precisión: ±2 [1/min]
Alarma: 20 a 350 [1/min]

CURVA RESPIRATORIA
Método impedanciométrico.
Frecuencia respiratoria:
•Rango de monitoreo para adulto: 0 a 120 [1/min]
•Rango de monitoreo para niño/neonato: 0 a 150 [1/min]
Dentro de 7 [1/min] – 150 [1/min], el error de medición es ±2 rpm o ±2%, cualquiera sea superior.
La tolerancia no es definida por otros rangos.
Especificaciones límite de la alarma: Rango.


Alarma de Apnea

PRESIÓN NO INVASIVA
Método Oscilométrico Automático
Modo de medición: Manual, auto (cíclico) o continuo (no apto para neonatos)
Unidad de medida: mmHg
Rango nominal de monitoreo:
•Rango Adulto: Sistólica: 40 – 270 mmHg,
Diastólica: 10 – 215 mmHg,
Media: 20 – 235 mmHg
•Rango Pediátrico: Sistólica: 40 – 200 mmHg,
Diastólica: 10 – 150 mmHg,
Media: 20 – 165 mmHg
•Rango Neonatal: Sistólica: 40 – 135 mmHg,
Diastólica: 10 – 100 mmHg,
Media: 20 – 110 mmHg
Especificaciones límite de alarma:
Rango








Precisión:
El error medio debe ser inferior a 5mmHg
La desviación estándar debe ser inferior a 8mmHg.
Inicio manual o automático de la medición a intervalos programables de 1/ 2/ 2.5/ 3/ 4/ 5/ 10/ 15/ 30/ 60/ 90/ 120/ 180/ 240/ 480/ 720min.
Tiempo de medición bajo modalidad continua: 5 min
Protección contra sobrepresión:
•Adulto: Cuando la presión del brazalete excede 297 mmHg ±3mmHg, la válvula de control aliviará la presión.
•Niño: Cuando la presión del brazalete excede 240 mmHg ±3 mmHg, la válvula de control aliviará la presión.
•Neonato: Cuando la presión del brazalete excede 147 mmHg ±3mmHg, la válvula de control aliviará la presión.
Resolución: 1 mmHg.

TEMPERATURA
Método de medición: directo.
Dos canales de temperatura.
Rangos de temperatura
Rango: 0 - 50° C
Precisión: ±0.1°C (exclusiva de tolerancia de sonda)
Resolución: 0.1°C
Alarmas de temperatura máxima y mínima: Rango.


ESPECIFICACIONES TÉCNICAS

Pantalla color táctil con tecnología TFT de 10.4" Resolución: 800 X 600
Pantalla inclinada para facilitar la observación.
Dimensiones: 291.7 mm x 250 mm x 146.5 mm
Peso 3.3 Kg. con batería
Fuente de alimentación: Dispone de una batería interna y una CA externa.
Tensión de alimentación:
100 – 240 Vac, 50/60 Hz.
C80/C50: Standard: Li-Ion 11.8V/2200mAh.
Una vez cargada completamente asegura funcionamiento continuo autónomo por 2 horas consecutivas.
Consumo: 60VA
Puertos de expansión reservados como por ejemplo para tarjeta SD, puerto USB y red.
Normas de calidad:
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, Clase 1, IPX1.
PACE Model 203 Dual Chamber (DDD) Temporary Cardiac Pacemaker OSYPKA
482,472.38 482,472.38 482472.38 ARS
GENERAL CHARACTERISTICS
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.

• 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
Pacing Modes:
- Primary: DDD, VVI, AAI, VDD
-Supplementary: D00, V00, A00, DVI
-DAI, VAT, AAT, DDD+AT, DAT


Syringe infusion pump model SN-50C6T: one channel, simplified support, with weight mode
140,072.63 140,072.63 140072.63 ARS
GENERAL CHARACTERISTICS
* It is characterized by its high precision, its 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 customized syringe information from 33 different manufacturers, Weigao and 32 other manufacturers, configurable by the user.
* The SN-50C6T pump, you can use sterile and disposable syringes of 10ml, 20ml, 30ml or 50ml. Automatically recognizes the syringe placed.
* The equipment can store up to 2000 historical infusion records, which include the following information: injection mode, injection speed, 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.
        Of residual limit.
        Occlusion
        End of injection.
        Without operation
        Empty syringe
        Flow limit exceeded.
        Plunger decoupled.
        Power cable disconnected.
        Of unloaded battery.
        Battery exhausted.
        Of system error.
* Operating time of the battery: starting from a full charge, the battery can support 6 hours of operation in a channel at a speed of 5 ml / h.
* Allows battery operation and charging from the car's 12Vdc connector.

TECHNICAL SPECIFICATIONS
Dimensions: (Length x Width x Height)
1 channel pump: 306mm x 140mm x 146mm
Weight:
1 channel pump: 2,25kg (includes support).
Feeding:
AC input: 100V ~ to 240V ~, 50/60 Hz.
DC input: 12Vcc.
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 the A.N.M.A.T .: PM 1125-18.

ACCESSORIES
1 Power cable.
1 User's manual.
1 Content list.
1 Manufacturing quality certificate.
1 Guarantee card.
Comen CM300 three channels electrocardiograph
78,645.61 78,645.61 78645.61 ARS

Designed for the automatic measurement, analysis and interpretation of the patient's electrocardiogram, with the impression of the diagnosis and its report.
CHARACTERISTICS
Intended to be used in medical institutions such as mobile units.
Lightweight, robust, compact and transportable, with handle incorporated into the cabinet.
On-screen display of the electrocardiogram, high resolution screen 320 x 240 pixels.
It contains powerful analysis and diagnostic software.
Introduction of patient data: name, gender, age, weight, height.
Digital filtering technology: high precision filter to eliminate interferences of various types and decrease to the deviation of the baseline.
Manual and automatic derivation selection mode.
Heart rate measurement by selected derivation.
Printing of three channels or three channels plus heart rate. Various printing formats.
Thermal printer with 80 mm paper, with selectable print speed and duration.
Visual alarms for lack of paper, low battery and cable disconnection.
Storage of 60 ECG records.
Safe design: ECG amplifier referred to ground, for total patient and operator safety.
Rechargeable battery with 2 hours of autonomy.
Optional: connection to data network.
ACCESSORIES INCLUDED WITH THE EQUIPMENT
1 Power cable.
1 patient cable with 10 clips.
6 Chest electrodes.
4 Limb electrodes.
1 Cylinder for paper.
1 Thermosensitive paper roll.
1 Cable to ground.
CERTIFICATES
• Certified Quality Standard:
ISO13485.
Disp. A.N.M.A.T. 3266/2013: B.P.F.
Disp. A.N.M.A.T. 2318/02.
CE certification
• Safety rules:
IEC 60601-1 (Eq IRAM 4220-1 and IEC 601-1- Req.
IEC 60601-1-2 (Electromagnetic Compatibility).
IEC 60601-1-4 (Programmable Medical Devices).
IEC 60601-2-25 (ECG).
IEC 60601-2-51 (ECG registration).
C30 Emergency transport monitor Comen
217,933.63 217,933.63 217933.63 ARS
Modelo C-30
Especificaciones Técnicas
Seguridad
ISO 13485: 2003 Aprobado
Marcado CE conforme a MDD93/42/EEC

Características físicas:
Dimensiones: 190mmX81.6mmX107mm
peso: 1.2 kg

Ambiente de Operación
Energía: 15Vcc
Alimentación: 100-250Vca, 50/60 Hz.
Temperatura: 0-40 °C
Humedad: 15-85%
Batería: Litio-ion, recargable
Batería Plug & play, capacidad: 2600mA
Máximo de 6.5 horas para la carga;
4 horas de trabajo continuo

Especificaciones
Paciente: adulto, pediátrico, neonato
Pantalla: 4.3" color TFT de pantalla táctil
Resolución: 16:9
2 curvas en pantalla
Velocidad de barrido: 12,5 mm/s, 25 mm/s, 50mm/s
Indicadores:
Luz indicadora de batería
Luz de alarma doble indicador
Bip de QRS y sonido de alarma
Sonido de teclas
Frente a otras: los parámetros del cable entre la cara
AC toma de entrada
Red entre la cara
MDR
Tendencia: 48 horas
Alarma: ajustable por el usuario los límites de alta y baja
Conexión a la central de monitoreo
Conexión a DVI

Respiración
Método impedanciométrico
Frecuencia: adulto 0-lOOrpm
neonatal 0-150rpm
Resolución: ± 1 rpm
Alarma de apnea:10s-40s
Alarma sonora y visual
Velocidad de barrido: 12.5,25mm/s
Selección de ganancia: x0.25, x0.5, x1, x2

ECG
Cable: CardioTecTM de 12 derivaciones,
3 o 5 broches (seleccionable)
12 derivaciones: I, Il, III, aVR, aVL, aVF, V1, V2, V3, V4, V5, -V6
5 broches: RA, LA, RL, LL, V o R, L, N, F, C,
3 broches: RA, LA, LL o R, L, F
Selección de Derivaciones: 12 derivaciones: I, II, III, aVR, aVL, aVF, V1, V2, V3, V4, V5, V6
5 broches: I, Il, IIl, aVR, aVL, aVF, V
3 broches: I, Il, III
Selección de ganancia:x0.25, x0.5, x1, x2, auto
Adulto: 15-300 1/min
Pediátrico/neonato: 15-350 1/min
Precisión: ±1% o ±1 1/min (el que sea mayor)
Resolución: 1 1/min
Ancho de banda de ECG:
MON: 0.5-55Hz
DIA: 0.05-150Hz
OPE: 1-20Hz
ST detección de segmentos: ±2.0mV (automático)
Análisis de Arritmia
Detección de pulsos de marcapasos

Temperatura
2 canales
Sensor estándar: Cutáneo
Rango de medición: 0-50 °C
Resolución: 0,1 °C
Precisión: 0,1 °C (excluye de error del sensor)
Canal: T1, T2, TD (diferencia de temperatura)

PNI
Método de medición: Oscilométrico automático
Modo de trabajo: manual/automático/Continuo
Intervalo: Ajustable de 1 min a 480 min
Tipos de medidas: sistólica, diastólica, media
Unidad de medida: mmHg/KPa, ajustable
Rango de la presión sistólica:
Adulto: 40 a 270mmHg
Pediátrico: 40 a 200mmHg
Neonato: 40 a 135 mmHg
Rango de la presión diastólica:
Adulto: 10 a 215mmHg
Pediátrico: 10 a 150mmHg
Neonato: 10 a 100 mmHg
Rango de media presión:
Adulto: 20 a 235mmHg
Pediátrico: 20 a 165mmHg
Neonato: 20 a 110mmHg
Protección contra sobrepresión: Hardware y software
Precisión: menos que ± 5 mmHg
Resolución: 1 mmHg

Sp02 Comen
Rango: 1-100%
Resolución: 1 %
Precisión: ± 2% (70-100%, Ped, sin movimiento)
± 3% (70-100%, Neo, sin movimiento)
0-69% sin especificar
Alarma de rango: 0-100%
Frecuencia de Pulso:
Rango: 20 a 300ppm
Resolución: 1 ppm
Precisión: ± 3ppm (sin movimiento)
± 5ppm (movimiento)
Alarma: 20 a 300ppm

EtCO2
CO2 de Flujo Lateral (SideStream)
Rango: 0 a 150 mmHg, 0 al 79%,
0 a 20kPa (a 760mmHg)
Precisión: ± 2mm Hg (0-40mmHg)
± 5% de la lectura (41-70mmHg)
± 8% de la lectura (71-100mmHg)
± 10% de la lectura (101-150mmHg)
Frecuencia: 0-120 rpm
Precisión: ± 2rpm (0-70rpm)
± 5rpm (> 70rpm)
Tiempo de respuesta: <240msec (10% a 90%)
Tiempo de retardo: <2s

C02 Comen de Flujo Principal
Rango: 0 a 150 mm Hg, 0 al 79%,
0 a 20kPa (a 760mmHg)

Precisión: ± 2 mmHg (0-40mmHg)
± 5% de la lectura (41-70mmHg)
± 8% de la lectura (71-100mmHg)
± 10% de la lectura (101-150mmHg)
Frecuencia: 0-120 rpm
Precisión: ± 2rpm (0-70rpm)
± 5rpm (>70rpm)
Tiempo de retardo: <2s
Syringe infusion pump model SN-50T66, three channels, standard support
363,151.25 363,151.25 363151.25 ARS
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.
Monophasic  3850B Defibrillator Monitor
260,572.81 260,572.81 260572.81 ARS
CARACTERÍSTICAS
MONITOR
Monitor de electrocardiograma con pantalla LCD.
Señal de Electrocardiograma adquirida por cable a paciente o por paletas.
Derivaciones:
- Con cable de 3 broches: DI, DII, DIII y PAL.
- Con cable de 5 broches: DI, DII, DIII, aVR, aVF, aVL, precordial y PAL.
Electrocardiograma en cascada.
Indicador digital de frecuencia cardíaca.
Indicador de batería baja.
Indicador luminoso de batería en carga.
Tecla de silencio de alarmas.
Alarmas de frecuencia cardíaca de 20 [1/min] a 250 [1/min].
Ganancia de ECG: 1/6, 1/4, 1/2, 1 y 2 cm/mV.

DESFIBRILADOR
Onda Monofásica
Uso del Desfibrilador en tres pasos:
1- Encendido y selección de energía.
2- Carga.
3- Disparo de energía por medio de pulsadores en paletas o desde teclado.
Llave de selección de carga por pasos: 2, 3, 5, 7, 10, 20, 50, 100, 200, 300 y 360 Joules.
Indicación auditiva y visual de final de carga.
Indicación de energía almacenada en display.
Disparo de energía presionando simultáneamente ambos pulsadores de paletas o la tecla de “DISPARO”.
La anulación interna de carga ocurre al apretar la tecla "ANULAR CARGA" o al dejar transcurrir 60 segundos desde el fin de carga de energía o al pasar la llave selectora de energía a la posición de "MONITOR" o "APAGADO". La energía se descarga internamente sin estar presente en paletas.
Descarga libre o sincronizada.
Indicación auditiva y visual del modo sincrónico.
Capacidad de descarga: 80 descargas a energía máxima, con la batería interna a plena carga.
Tiempo de carga a 360 J: menor a 6 segundos.
Conexión a paletas internas o a parches de desfibrilación.
El equipo cuenta con test de energía entregada.

MARCAPASOS TRANSCUTÁNEO
Estimulación externa a través de electrodos.
Frecuencia: 40 ppm a 180 ppm (seleccionable en pasos de 5 ppm).
Corriente: 10 mA a 200 mA (seleccionable en pasos de 5 mA).
Modo: Seleccionable, a demanda o fijo.
Ancho de pulso: 20 ms ± 5%.

SATURACIÓN DE OXÍGENO (SpO2)
Medición de SpO2:
- Rango: 0% a 100%.
- Exactitud: Adulto ± 2% entre el 70% y 100%. Neonatal: ±3% entre el 70% y 100%. En movimiento: ±3% entre el 70% y 100%.
- Resolución: 1%.
- Alarma de saturación porcentual de oxígeno
Límite superior: 1 a 100.
Límite inferior: 0 a 99.
- Medición de frecuencia de pulso y alarmas desde 30 a 250 [1/min] ± 3 [1/min] y ±5 [1/min] en movimiento.
- Resolución: 1 [1/min].

ESPECIFICACIONES TÉCNICAS
Tensión de alimentación: 90Vca a 240Vca - 50/60 Hz o 12 Vcc.
Batería interna recargable NiMh - 12V, 3500 mAh.
Consumo 180 W (7W durante la espera).
Tamaño: 295mm (ancho) x 200mm (alto) x 345mm (largo).
Peso: 6 kg (incluyendo paletas externas, batería y registrador).

CERTIFICACIONES
Normas de Calidad:
- ISO13485 (certificada).
- Disp. A.N.M.A.T. 3266/2013: B.P.F.
- Disp. A.N.M.A.T. 2319/02.

Normas de Seguridad:
- EN 60601-1 (Eq. IRAM 4220-1 e IEC 601-1).
- EN 60601-1-2 (Compatibilidad Electromagnética).
- EN 60601-1-6.
- EN 60601-1-8.
- EN 60601-2-4.
- EN 60601-2-27.
- EN 60601-2-49.
- ISO 80601-2-61.
Autorizado por la A.N.M.A.T. PM-1125-4.

ACCESORIOS INCLUIDOS
1 juego de paletas externas para adultos.
1 Cable de alimentación para entrada de +12 Vcc externos.
1 Cable de alimentación de línea.
1 Cable a paciente de 3 o 5 broches para ECG.
10 electrodos descartables.
1 Manual de uso.
1 Juego de electrodos y 1 cinto elástico.
1 Sensor pinza de oximetría, adulto ó pediátrico.
1 Prolongador de sensor de oximetría.
Monitor Desfibrilador 3850B Monofásico (copia)
0.00 -0.0 ARS
Desfibrilador de simulación. NO DESCARGA ENERGÍA.

CARACTERÍSTICAS
MONITOR
- Monitor de Electrocardiograma con pantalla LCD.
- Señal de Electrocardiograma adquirida por cable a paciente o por paletas.
- Derivaciones:
- Con cable de 3 broches: DI, DII, DIII y PAL.
- Con cable de 5 broches: DI, DII, DIII, aVR, aVF, aVL, Precordial y PAL.
- Electrocardiograma en cascada.
- Indicación digital de frecuencia cardíaca.
- Indicador de batería baja.
- Indicador luminoso de batería en carga.
- Tecla de silencio de alarmas.
- Alarmas de frecuencia cardíaca de 20 [1/min] a 250 [1/min].
- Ganancia de ECG: 1/6, 1/4,1/2, 1 y 2 [cm/mV].

DESFIBRILADOR
- Uso del Desfibrilador en tres pasos:
1. Encendido y selección de energía.
2. Carga.
3. Disparo de energía por medio de pulsadores en paletas o desde teclado.
- Llave de selección de carga por pasos: 2, 3, 5, 7, 10, 20, 50,100, 200, 300 y 360 [Joules].
- Indicación auditiva y visual de final de carga.
- Indicación en display de energía almacenada.
- Disparo de Energía presionando simultáneamente ambos pulsadores de paletas o la tecla “DISPARO”.
- Anulación interna de carga:
Ocurre al apretar la tecla “ANULAR CARGA” o al dejar transcurrir 60 segundos desde el fin de carga de energía o al pasar la llave selectora de energía a la posición de “MONITOR” o “APAGADO”.
- No realiza descargas pero puede, para la simulación, configurarse como libre o sincronizada.
- Indicación auditiva y visual del modo sincrónico.

REGISTRADOR
- Tecla directa de registro.
- Registro automático ante un evento.
- Registrador térmico de alta resolución.
- Velocidad de Registro: 25 mm/s.
- Imprime: fecha y hora, energía en Joules, Curva de Electrocardiograma, Ganancia, Frecuencia Cardíaca, Derivación, Velocidad de Barrido, Curva pletismográfica, SpO2, Frecuencia de Pulso, Modo, Frecuencia de Marcapasos, Corriente de Marcapasos.
- Papel: Ancho de 50 mm, Diámetro máximo de 45 mm.

MARCAPASOS TRANSCUTÁNEO
- Estimulación externa a través de electrodos.
- Frecuencia: 40 ppm a 180 ppm. (Seleccionable en pasos de 5 ppm).
- Corriente: 10 mA a 200 mA. (Seleccionable en pasos de 5 mA).
- Modo: Seleccionable, a demanda o fijo.
- Ancho de pulso: 20 ms ± 5%.

SATURACIÓN DE OXÍGENO (SpO2)
- Medición de SpO2:
- Rango 0% a 100%.
- Exactitud:
Adulto ±2% entre el 70% y 100%.
Neonatal ±3% entre el 70% y 100%.
En Movimiento ±3% entre el 70% y 100%.
- Resolución: 1%.
- Alarma de saturación porcentual de oxígeno:
Límite superior: de 1 a 100.
Límite inferior: de 0 a 99.
- Medición de frecuencia de pulso y alarmas desde 30 a 250 [1/min] ±3 [1/min] y ±5 [1/min] en Movimiento.
- Resolución: 1 [1/min].

ESPECIFICACIONES TÉCNICAS
- Tensión de alimentación: 90 Vca a 240 Vca - 50 Hz/60 Hz, o 12 Vcc.
- Batería interna recargable NiMh - 12 V, 3500 mAh.
- Consumo: 10 W.
- Tamaño: 295mm (ancho) x 200mm (alto) x 345mm (profundidad).
- Peso: 5 Kg (Incluyendo Paletas externas, batería y registrador).

ACCESORIOS INCLUIDOS
- 1 juego de paletas externas para adultos con cable espiralado.
- 1 cable de Alimentación para entrada de +12 Vcc externos.
- 1 cable de Alimentación de línea.
- 1 cable a paciente de 3 broches o de 5 broches para ECG.
- 10 electrodos descartables.
- 1 Manual de Uso.
- 1 Juego de electrodos y 1 cinto elástico.
- 1 rollo de papel de 50 milímetros.
- 1 Sensor pinza de oximetría, adulto ó pediátrico.
- 1 Prolongador de sensor de oximetría.