Specifications:
Material: Polyvinyl chloride (PVC).
Disposable.
Graduations.
Endotracheal tube shall meet the required standards describing the dimensions, the tube characteristics, tube point and the tube markings.
Endotracheal tube with:
Open distal end and Magill-type point with oral angle of 37.5º.
Standard connector (ext. Ø 15mm) at the proximal end enabling the tube to be connected to the ventilation system.
With Murphy's eye.
Sterile.
Initial sterilisation method: Ethylene oxide gas or Gamma radiation.
Endotracheal tube without cuff.
Size: Ø internal 3.5mm.

Instructions for use:
Sterile Endotracheal tube:
Device used to correct a deficiency in respiratory function during general anaesthesia or resuscitation.
Inserting the endotracheal tube must be done only by staff trained in resuscitation practice.
Device designed to be introduced into the trachea via the mouth or nose in order to link the trachea (upper respiratory tract) to the outside air, giving the possibility to provide ventilation assistance to patient (manual or mechanical).
Lubricate the distal end of the endotracheal tube and the distal 1/2 of the Endotracheal Tube Introducer (Bougie)
Intended for endotracheal tubes for adults or children depending the diameter.

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SPECIFICATIONS
Nasal cannula (nasal prongs), device designed for easy administration of oxygen into the patient nose through two small prongs placed in the nostrils, providing comfort for the patient.

The device consists of:
Material: Preferably soft and kink resistant polyvinyl chloride (PVC).
Soft twin prongs nasal tips to ensure equal oxygen flow to both.
Soft funnel shaped connector to facilitate easy connection to oxygen source.
Adjustable, smoothly finished nasal tips for maximum patient comfort.
Length of the oxygen tube: +/-2 m.
Single use.
Non-sterile.
Star lumen main tube to avoid accidental blockage.
Over-the-Ear tubing adjustable
Size selected: Adult

INSTRUCTIONS FOR USE:
Care should be taken to keep the nostrils clear of mucus, which could block the flow of oxygen.
Nasal cannula used to deliver oxygen directly to the patient via two small prongs placed in the nostrils
Place the twin prongs inside the nostrils and secure them with a piece of tape on the cheeks near the nose and adjust the harness (Over-the-Eartubing).
It is important to have the proper equipment to control low flow rate.
Set a flow rate of 1-2 l/min (0.5 l/min for young infants) to deliver an inspired oxygen concentration of 30-35%.
Humidification is not required with nasal prongs.

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DESCRIPTION:
Neonatal incubator, double-wall, electronic, automatic, mobile, with accessories

TECHNICAL SPECIFICATIONS:
Sturdy construction, mobile base with 4 anti-static swivel castors and 2 brakes
Protective side/corner bumpers
Double-wall neonatal incubator, mobile
Automatic servo-control and manual control
Mould and corrosion resistant frame
Suitable for frequent and easy dismantling and cleaning
Side rails, IV pole and instrument shelf
Cabinet with 2 drawers, integrated in the base
Side handles for easy moving

Canopy:
Inclined front, with access door and 2 port holes
2 rear port holes
double-wall
radio-transparent
4 (min) apertures for cables and tubing
Silent incubator and door / port holes operation
Dimensions 45 W x 80 L x 43 H cm (minimum guaranteed)

Mattress:
fixed mattress tray
tilting ± 12 degrees

Modes:
Servo-controlled, air temperature
Servo-controlled, skin temperature
Manual

Skin temperature sensor accuracy ± 0.3 ºC
Humidifier with integrated water chamber, passive not-adjustable (evaporation chamber) or servo-controlled adjustable humidifying system (up to 95 % relative humidity) depending on the available incubator model
Air temperature setting 25 – 37 ºC, override up to 39 ºC, with 0.1 ºC increments
Temperature variability (fluctuation between set and real values) ± 0.5 ºC
Temperature uniformity (at mattress level) < 0.8 ºC
Skin temperature setting 34 – 36 ºC, override up to 38 ºC, with 0.1 ºC increments
Warm-up time (to 37 ºC in 22 ºC ambient temperature) < 30 min
Air velocity over the bed < 0.35 m/s
Automatic self-test and continuous system monitoring
Control panel and display, visualisation of settings and measured parameters
Audio-visual alarms for skin/air temperature, sensors, fan, heater, system functionality
Air filter capacity at inlet 99 % particles > 0.5 um
Power requirements 110 – 220 V / 50 – 60 Hz
Power consumption 600 – 750 W
Noise level inside the incubator < 55 dB

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DESCRIPTION:
Neonatal warming system, nest-type with water mattress and heating pad, portable, basic set

TECHNICAL SPECIFICATIONS:
Integrity testing of all system parameters every 5 minutes.
Flexible waterproof low voltage heating pad slides under mattress.
Pre-set is 37°C, Adjustable from 35 to 38°C in increments of 0,1°C.
The Warmer is used to assist premature babies maintaining the appropriate body temperature.
System consists of a control unit, a heating pad, a water mattress and an inflatable BabyNest frame.
Electronic servo temperature control.
Perform self-testing of all functions and internal safety circuit by switching the control unite.
Accuracy temperature control of heating pad is ±0.1°C.
Automatic warm-up to 37°C, time to stabilize approx. 20 min (starting at 20°C). (Warm up time is shortened if water mattress is filled with lukewarm water at start).
Large colour display shows operational status, with set and measured values.
Over Temperature Alarm: at a water temperature of 39.5 ±1 °C. Warming capacity: About 4-5°C per hour. (Room temperature about 22°C and filled with 4,5 liters of water and placed on the mattress of a baby bed and covered with the nest and a sheet. Connection to mains or a 24V battery.)
Strong soft plastic BabyNest mattress fills with water (about 36°C), approx. 4.5 L.
Reusable BabyNest frame keeps baby in place.
Cotton cover frame can be tightly secured around the water mattress and heating pad.
The water mattress will cool 1°C per hour which means that one has about 2 hours to restore power.
External battery connection point at the underside of the control unit.

Heating Pad:
Material: PVC.
Voltage: 24-volt DC from control Unit BW-50 007 when powering with mains power or 24V DC when powering from 12-24V battery source.
Power requirements: 110-240 V AC or 110-120 V AC.
Battery 12 or 24 V.
Power consumption 50 Watt. (10 Watt when the Control Unit is powered from a 12 Volt battery)
Frequency 50 or 60 Hz,

Baby Nest:
Material: Cover, high quality cotton and polyester.
Washing: Recommended temperature 60°C, can tolerate 90°C but might shorten lifetime.

Water Mattress:
Material: Medical Grade PVC.

Control Unit:
Temperatures available: 35 to 38°C increments of 0.1°C.
Auditory Alarm: 55 dB sound level.
Main Power/frequency: 110-240 V AC or 110-120 AC. 50/60 Hz.
Battery power: 24 V DC, 12 V DC (with limited warming capacity)
Internal Battery: Alkaline, 1.5V size LR6 (AA) (only for power failure alarm.
Indication of temperatures and alarms:
Over temperature alarm at water Temperature of 39.5 ±1 °C.

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DESCRIPTION:
External defibrillator for adult and paediatric patients, with ECG monitor and printer, synchronised and bi-phasic, portable, AC and battery powered, with accessories.

TECHNICAL SPECIFICATIONS:
Suitable for adult and paediatric patients
Supplied with adult and paediatric pads/adapters
External defibrillator with ECG monitor
Non-directional pads, suitable for bi-phasic impulse waveform

Defibrillator features:
Patient resistance 30 – 175 Ohm (minimum guaranteed range)
Load compensation, energy level automatic adjustment to the patient impedance
Manual and synchronised defibrillation
bi-phasic energy waveform
Energy output accuracy ± 15 %
Adult and paediatric energy settings
Energy output range 2 – 200 J or 2 – 360 J.
Adjustable energy output, by steps
Charge time to maximum energy < 10 s (mains power supply and battery charged)

ECG monitor:
ECG gain 2.5, 5, 10 and 20 mm/mV (minimum guaranteed)
Protection against defibrillation discharges
Detection through pads or dedicated ECG cable
ECG waveform and analysis, selectable visualisation modes
3-leads ECG cable
Adjustable ECG print modes and settings (real-time, manual)

Printer:
Paper width 58 or 72 mm, depending on the available model
Internal safety discharge feature 
Built-in 3-channel thermal printer
Print of ECG curves and analysis, events, settings and alarms
Paper speed 25 mm/s 
Compatibility with additional modes and monitoring features, not included (SAED, AED and pace modes, SpO2)

Internal storage for ECG, events (at least 500 or 60 min monitoring) and parameters
Integrated control panel with all parameters and controls
Display, backlit flat panel, 5 – 8 inch 
Data/USB communication interface
Audio/visual alarms for pads connection, mains/battery power supply status, paper and printer status, system errors
Automatic and manual self-test, continuous check of pads and electrodes connection
Visualisation of defibrillation mode, energy, ready/charging state, ECG curves and heart rate, date/time, settings, mains and battery status, system messages and alarms
Automatic switch to battery in case of power failure, automatic recharge on connection to mains
Integrated battery charger and transformer
Integrated carry handle
Splash and shock resistant
Power requirements 110 – 220 V / 50 – 60 Hz
Power consumption 200 W
Removable rechargeable battery
Battery autonomy > 100 shocks at 200 J or 3.5 h monitoring

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DESCRIPTION
Nebulizer Compressor-driven, portable, AC powered with accessories

TECHNICAL SPECIFICATIONS
Integrated drug reservoir, capacity 2 - 6 ml, residual volume: 2 ml
Median Mass Aerodynamic Diameter (MMAD) of particles: 2.44 – 3.16 µM
Portable, compressor-driven nebulizer, for the treatment of upper/lower respiratory system and for the delivery of nebulized drugs
Maintenance-free and oil-free compressor pump
Air inlet filter
Noise level: ≤ 55 dB
Power requirements 220 V / 50 Hz
Sturdy construction, suitable to be disinfected with hospital-grade products
Device is provided with accessory storage compartment
Air flow under load: 5 – 6 l/min
Drug nebulization flow 0.2 – 0.4 ml/min 
Power consumption: ≤ 170 W

OPERATING ENVIRONMENT
Operating conditions: 10 - 40°C / 90% relative humidity
Storage conditions: 0 - 50°C / 90% relative humidity

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Oxygen Concentrators are not suitable to be used as an oxygen source to other medical equipment providing respiratory support, such as ventilators, CPAP devices, High Flow Nasal Oxygen, etc.

SPECIFICATIONS:
Provides continuous flow of concentrated oxygen 93%
Oxygen sensing device is integrated and measures concentration at flow meter entrance.
Device concentrates oxygen from ambient air
On 4 antistatic swivel castors, 2 with brakes
Integrated handle allows for easy moving and positioning
Flowmeter range: 1 to 10 LPM
Flowmeter continuously adjustable with markings at 0.5 L intervals
Continuous monitoring, with visual and audible alert on:
Low/ high output pressure, no flow, low oxygen concentration <82%, power failure
Sound level produced: less than 52 dB (A)
Maximum output flow: 10 LPM
Output pressure: min 55 // kPa. 0.04/0.07
Power requirements: 220V-240V, 50Hz-60Hz or 110V 50/60Hz
Digital or analogue meter to display cumulative hours of device operation
User interface easy to operate with numbers and displays that are clearly visible
Device weight: 28 kg
Oxygen outlet durable, with approx.6mm barbed fitting or equivalent

ENVIRONMENTAL CONDITIONS
Storage conditions: e: -40 °C to 55°C / RH: ≤ 95%
Operating altitude: 0 to 2286m above sea level
Operating conditions: 10 to 40°C / RH: 15 to 85%

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DESCRIPTION:
Neonatal resuscitation table, mobile, with warmer and accessories

SPECIFICATIONS:
Side handle for easy moving
Integrated support for 2 x 10 l oxygen cylinders
Side rail and IV pole for mounting accessories and equipment
Mobile resuscitation table for neonatal patients, with warmer
Sturdy construction, with 4 anti-static swivel castors and 2 brakes
Side panels, transparent acrylic resin, collapsible/foldable for complete accessibility
Vertical column with controls and display
With lower drawer for storage

Table:
Mattress cover flame-retardant, waterproof and cleanable with
Surface 60 W x 76 L cm (minimum guaranteed dimensions)
Hospital-grade disinfection products
Mattress covering the entire table surface, thickness 5 cm

Heating system:
Reflector and safety grid
Integrated cradle heating
Overhead radiant heater, fixed height
Radiant heating by quartz/ceramic elements, parabolic
Uniform heat distribution

Lighting system:
With 2 x halogen additional spot examination lights
Integrated in the overhead radiant heater

Modes:
Pre-warming function
Instant switch between manual and servo modes
Servo-controlled, electronic and driven by skin temperature
Manual
Skin temperature setting 34 – 38 ºC, with 0.1 ºC increments (servo mode)
Skin temperature sensor accuracy ± 0.3 ºC
Power requirements 220 V / 50 Hz
Displayed parameters: mode (manual or servo), heating power (%), pre-set temperature, actual skin temperature, air temperature in the cradle
Audio-visual alarms for skin temperature, heating system and sensors failure
Display panel, integrated in the column, visualising working parameters and alarms
Power consumption 1,100 W
Manual and pre-heating settings 10 – 80 % by 10 % steps

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