Resuscitation & Anaesthesiology Equipment, Resuscitation & Anaesthesiology Equipment Equipments, Resuscitation & Anaesthesiology Equipment Tools, Resuscitation & Anaesthesiology Equipment Tool Kits, Resuscitation & Anaesthesiology Equipment Manufacturers, Resuscitation & Anaesthesiology Equipment Suppliers from India, China, Kenya
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Syringe pumps ensure highly accurate volume delivery and consistent flow for small volumes (≤60 mL) of potent pharmacologic agents that are typically delivered at flow settings between 0.5 and 10 mL/hr. Syringe infusion pumps are used to administer intravenous (IV) fluids such as antibiotics, regional anaesthetics, antiarrhythmic medications, and chemotherapeutic agents.
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Vital signs monitors are used to measure basic physiologic parameters and track the status of low-acuity patients (patients found in medical-surgical areas, emergency departments, and ambulatory care centres) so that clinicians can be informed of changes in a patient's condition.
Patient vital signs monitor, 6 parameters, suitable for adults, paediatric/infants and newborn patients.
Mobile LED phototherapy unit AC powered including accessories. Jaundice, a yellowish discoloration of the skin, eyes, and mucous membranes, is a major symptom observed when bilirubin levels in blood rise above 5 mg/dL. Phototherapy units are used to treat hyperbilirubinemia, a condition characterized by high bilirubin concentrations in the blood. Bilirubin, a product of haemoglobin breakdown, remains in the body until the liver can convert it to a form that can be excreted.
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In general, infusion pumps are used when the solution to be administered must be delivered with greater accuracy than can be provided through a manually adjusted gravity administration set. Infusion pumps are used to accurately deliver liquids through intravenous (IV) or epidural routes for therapeutic and/or diagnostic purposes. They are used in hospitals, in alternative care settings (e.g., homes, long-term care facilities, physicians' offices, outpatient infusion centres), and, occasionally, in emergency medical service vehicles. Volumetric single channel infusion pump, AC and battery powered including accessories.
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Newborn resuscitation and support of transition of infants at birth. Additionally, used to provide thermal support for newborns in the delivery suite and for critically ill infants who require constant nursing intervention. Mobile resuscitation table for neonatal patients equipped with a radiant warmer and supplied with accessories.
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Anaesthesia units are highly complex devices requiring specific infrastructure provision to be able to operate. They need a scavenging system, pipped medical air supply, and oxygen and nitrous oxide sources which can be piped or from cylinders. In addition, these machines require trained operators and technicians to carry out preventative maintenance so the units can operate safely.
The patient is anesthetized by inspiring a mixture of O?, the vapor of a volatile liquid halogenated hydrocarbon anaesthetic, and, if necessary, N?O and other gases. Because normal breathing is routinely depressed by anaesthetic agents and by muscle relaxants administered in conjunction with them, respiratory assistance is also provided via either an automatic ventilator or by manual compression of the reservoir bag.
Anaesthesia units dispense a mixture of gases and vapours and vary the proportions to control a patient's level of consciousness and/or analgesia during surgical procedures. Anaesthesia units primarily perform the following four functions:
- Blend gas mixtures, in addition to O?, that include air or nitrous oxide (N?O) along with an anaesthetic vapor.
- Facilitate spontaneous, controlled, or assisted ventilation while using these gas mixtures.
- Provide oxygen (O?) to the patient
- Reduce, if not eliminate, anaesthesia-related risks to the patient and clinical staff.
An electrically powered device designed to deliver high-flow (exceeding peak inspiratory flow) heated and humidified ambient air or air/oxygen to a neonatal patient as part of non-invasive ventilation (NIV); it may additionally be used with a water tank to produce bubble continuous positive airway pressure (bubble CPAP). It is intended for use by a healthcare provider on a spontaneously breathing patient in hospital settings. It consists of a medical air input, an oxygen input, an electronic gas mixer, a heating element, and humidification chamber.
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Fully automated external defibrillators (AEDs) deliver a high-voltage electrical impulse to the heart in order to restore normal rhythm and contractile function in patients who are experiencing ventricular fibrillation (VF) or ventricular tachycardia (VT) that is not accompanied by a palpable pulse. AEDs are designed for use primarily by first responders to cardiac emergencies, who may not be fully trained in advanced cardiac life support (ACLS). In the prehospital setting, these emergency personnel can include EMTs, firefighters, and law enforcement officers. Flight attendants, security guards, and others −sometimes called targeted responders may be expected to use PAD units. AEDs differ from conventional manual defibrillators in that AEDs can analyse the ECG rhythm to determine whether defibrillation is necessary; this eliminates the need for the user to interpret the cardiac rhythm before delivering a shock. AEDs can also be used in areas of the hospital where advanced life support personnel are not readily available.
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An ECG monitor included with the unit is used to verify the presence of a shockable rhythm and the effectiveness of treatment. Defibrillators deliver a high-voltage electrical impulse to the heart in order to restore normal rhythm and contractile function in patients who are experiencing ventricular fibrillation (VF), ventricular tachycardia (VT), or another shockable rhythm.
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A warming unit using a heated mattress and a nest type frame to raise or maintain a newborns’ or premature babies body temperature through conductive heating. A liquid bases warmer system to assist premature babies maintaining the appropriate body temperature.
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An infant incubator provides a closed, controlled environment that warms an infant by circulating heated air over the skin. Incubators feature better temperature control than radiant warmers (overhead heating units), which can overheat or underheat the infant. However, an infant in an incubator is less accessible to the caregiver. The heat is then absorbed into the body by tissue conduction and blood convection. Ideally, both the skin and core temperatures should be maintained with only minor variations.
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Infant radiant warmers are commonly used to provide thermal support for newborns in the delivery suite, for critically ill infants who require constant nursing intervention, and for infants undergoing treatment that prolongs exposure to a cool environment.
Radiant warmer, newborn, with accessories.
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:
Star lumen main tube to avoid accidental blockage.
Over-the-Ear tubing adjustable
Soft funnel shaped connector to facilitate easy connection to oxygen source.
Adjustable, smoothly finished nasal tips for maximum patient comfort.
Soft twin prongs nasal tips to ensure equal oxygen flow to both.
Length of the oxygen tube: +/-2 m.
Material: Preferably soft and kink resistant polyvinyl chloride (PVC).
Single use.
Non-sterile.
Size selected: Adult
Nasal cannula (nasal prongs), device designed for easy administration o foxygen 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).
Star lumen main tube to avoid accidental blockage.
Over-the-Ear tubing adjustable
Soft funnel shaped connector to facilitate easy connection to oxygen source.
Soft twin prongs nasal tips to ensure equal oxygen flow to both.
Adjustable, smoothly finished nasal tips for maximum patient comfort.
Length of the oxygen tube: +/- 2 m.
Size selected: Child
Single use.
Non-sterile.
Nasal cannula (nasal prongs), device designed for easy administration ofoxygen into the patient nose through two small prongs placed in thenostrils, providing comfort for the patient.
The device consists of:
Soft twin prongs nasal tips to ensure equal oxygen flow to both.
Soft funnel shaped connector to facilitate easy connection to oxygensource.
Length of the oxygen tube: +/- 2 m.
Material: Preferably soft and kink resistant polyvinyl chloride (PVC).
Adjustable, smoothly finished nasal tips for maximum patient comfort.
Star lumen main tube to avoid accidental blockage.
Over-the-Ear tubing adjustable
Size selected: Neonate
Non-sterile.
Single use.
Basic hospital equipment for health structures and emergency situations in wards, emergency room, operating theatre, delivery room, intensive care unit, etc.
The suction pump should be operated only by a person who has received adequate training in pharyngeal and tracheal suction techniques.
High performance suction pump, foot-operated for pharyngeal and tracheal suction and during minor surgical interventions. Supplied with instruction manual and diagrams covering the function of the pump, how to use it, dismantle and assemble it, to clean, disinfect and sterilize it, its maintenance and spare-parts.
High performance, high quality, single piston portable foot-operated suction pump
For pharyngeal and tracheal aspiration, and other minor medical procedures
Piston, with diaphragm valve, is sealed with removable elastic O-ring
Large stable base is entirely fit with anti-slip, preventing the pump from gliding-away while in use
Vacuum, maximum: - 70 kPa (ca. - 700 mbar)
Pedal movement generates suction every time it’s depressed
Integrated spring, returns the pedal to its initial ready-to-use position
Lever minimises pedal force required to reach maximum flow
For operator’s comfort, pedal should support at least 20 cm of the foot, and distal-end displace maximum 9-11 cm
Container is transparent, allowing assessing collected volume
Wide opening at the top of the container allows for easy and thorough cleaning
Basic essential design without manometer
Air-flow, maximum: 30 to 40 L/min (such as at two pumping strokes per second)
Collection capacity container: 900-1100 ml
Operating temperature range: -20 C to +50 C
All parts can be autoclaved at 121 C
The suction pump set can be entirely disassembled, facilitating proper cleaning and disinfection.
Materials:
All parts are manufactured from high-strength, durable material, not requiring specific maintenance or storage conditions
Foot pedal: aluminium or equivalent sturdy plastic, fit with embossed anti-slip relief
Conical suction tip: Acetal or equivalent tough plastic
Aspirating tube: silicone rubber
Container: transparent polycarbonate or equivalent sturdy transparent plastic
Bottom: rubber or equivalent anti-slip material
Gasket, O-rings and valve diaphragm: silicone rubber or equivalent
Piston O-ring: Teflon or equivalent.
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.
Ventilator, Intensive Care, for adult, paediatric and neonatal patients, AC and battery powered, with accessories.
Mechanical ventilators are life support devices that move gas (e.g., air and/or oxygen) to and from a patient's lungs. In most cases, mechanical ventilators are used for a short period of time (a few days to a few weeks) to deliver pressurized medical gases to the patient's lungs to support gas exchange and rest ventilatory muscles until the patient is able to breathe without mechanical assistance. Some patients, however, require permanent ventilatory support. These devices may provide temporary or permanent respiration for patients who cannot breathe on their own, or who require assistance maintaining adequate ventilation because of illness, trauma, congenital defects, or the effects of drugs (e.g., anaesthetics).
Allows for precise oxygen delivery by utilizing different sized ports to change FiO2 (24 – 60%). Face mask to provide oxygen at flow rates up to 12 LPM. Also known as air-entrainment masks able to provide total inspiratory flow at a specified FiO2.
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Face mask to provide oxygen at flow rates up to 12 LPM. Allows for precise oxygen delivery by utilizing different sized ports to change FiO2 (24 – 60%). Also known as air-entrainment masks able to provide total inspiratory flow at a specified FiO2.
Allows for precise oxygen delivery, with specific concentrations ranging from 24-60%.
The kit of the mask includes the tubing, humidity cup and multiple jets, which are color-coded and indicate the percentage of oxygen.
Mask is soft, transparent, with well-fitting mould.
The nose clip is adjustable.
The tubing is terminated with standard or universal hose end connector.
Individually packed.
Tubing compatible with standard oxygen connection tubing.
Tubing length: 2 meters
Non-sterile.
Child size.
Single use.
The oxygen flow splitter is a device intended to distribute medical oxygen from a source to multiple independent outlets. It can be connected to any low-pressure oxygen source, including concentrators, cylinders and a centralized system, and is suitable for tabletop or wall mounting.
Suitable for cleaning and disinfection with hospital-grade cleaning products.
Inlet port is DISS format.
6 mm barbed outlets.
Flow meter columns are transparent, clearly readable and graduated (metric system).
Equipped with five independent, Thorpe tube flow meters, to measure and regulate the flow of medical gas.
Inlet pressure up to at least 20 psi (138 kPa).
0-2 L/min, accuracy better than 10%, graduation 0.125 L/min or lower.
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. A mains electricity powered device that concentrates oxygen from ambient air and delivers the concentrated oxygen in a controlled manner to a patient requiring oxygen therapy, up to 10 L/min.
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Suitable for professional clinical use, all patient categories neonate, infant, adult
Robust shock resistant design allow use in demanding environments
Ultra-compact pulse oximeter integrated into finger/toe clip
Measuring ranges:
SpO2 resolution: 1% or less
SpO2 accuracy within: +/-3%
SpO2 detection within the range of: 70 to 99%
Pulse rate accuracy: within: +/-3%
Pulse rate detection: 30 to 240 bpm
Pulse rate resolution: 1 bpm)
Enclosure protection IPX2 or better
Suitable for cleaning and disinfection with hospital-grade cleaning products.
Display shows SpO2, pulse rate, signal strength, sensor error or disconnect and low battery.
Power requirements two 1.5V AAA batteries
Accommodates finger/toe thicknesses 8 to 25mm directly or through the use of a separate sensor which can be connected to the device.
Spot-check of arterial blood oxygen saturation (SpO2) and heart rate(HR)
Batteries must allow at least 2500 spot-checks, calculated at 30 seconds per spot-check, or at least 21 hours of operation.
The unit is equipped with an automatic power off feature.
A sealed bottle of water inserted into a breathing circuit to add moisture to the breathing gases for administration to a patient. This type of humidifier does not heat the gas.
Graduated, transparent humidification bottle, shatter resistant.
Graduation shall show minimum and maximum water level.
Detachable metal or rigid durable polymer cap with gas connectors.
Non-heated, reusable humidifier for oxygen therapy and ventilation/anaesthesia inspiratory lines.
Bubble-through humidification system.
DISS connectors for gas inlet and outlet
All available adaptors for gas connection to be described in bid response
Flow rate capacity up to 15 L/min.
Safety pop-off valve incorporated.
Autoclavable and/or disinfectable with hospital grade detergents.
Humidification chamber working volume at least 150 ml, not greater than 500 ml.
Handheld, portable, battery powered pulse oximeter, continuously displaying patient oxygen saturation (SpO2) and pulse rate in real time using an external probe on the skin.
Display:
Display with main parameters: SpO2, pulse rate, plethysmographic waveform, signal quality, alarm messages, battery state indication.
Data update period for valid data displayed ≤ 15s.
Features:
Audible and visual alarms for low/high saturation and pulse rate.
Audible and visual alarms for sensor error or disconnected, system errors, low battery.
Suitable for cleaning and disinfection with hospital-grade cleaning products.
Alarm override and temporary silencing function.
Capable of working with adult, paediatric and neonatal reusable probes.
Enclosure protection IPX1 or better.
Device and probe weight < 200 g.
Measurement:
SpO2 and pulse rate monitor, with plethysmography waveform, for adults, children and neonates.
SpO2 resolution 1 %.
SpO2 accuracy (in the range 70 - 100%) within ± 3%, for all patients and perfusion / movement conditions.
SpO2 detection includes the range 70 - 100 %. Also capable of measuring lower saturations.
Pulse Rate detection includes the range 30 - 240 bpm.
Pulse Rate accuracy within ± 2 bpm or ± 2%.
Pulse Rate resolution 1 bpm.
Medical gas flow meter (Thorpe tube design) to regulate and measure the flow rate of medical gas supplied to a patient, maximum flow rate 3.5 LPM, for medical oxygen.
Transparent, graduated (metric system) column, shatter resistant polymer certified for medical use.
Graduation shall have over 270 degrees of visibility.
Needle valve and body constructed of brass or aluminium.
Inlet and outlet connectors DISS style, other types of connectors available upon request
Thorpe tube design flow meter using DISS input connector for panel /regulator mounting.
Can be cleaned with damp cloth and a disinfection solution.
Calibrated at 50-55 psi / 345-380 kPa / 3.4-3.8 bar inlet gauge pressure.
Inlet pressure (nominal) > 50 psi (345 kPa / 3.45 bar), peak inlet pressure at least 100 psi (690 kPa / 6.89 bar).
Maximum flow rate when fully opened: 50 L/min (depending on supplied model).
Pressure compensated design to give specified accuracy for whole range of input pressures
Built-in inlet filter (depending on supplied model).
Adjustment knobs to have rough surface to prevent slipping.
Medical gas flow meter (Thorpe tube design) to regulate and measure theflow rate of medical gas supplied to a patient, maximum flow rate 8 LPM,for medical oxygen.
Graduation shall have over 270 degrees of visibility.
Needle valve and body constructed of brass or aluminium.
Calibrated at 50-55 psi / 345-380 kPa / 3.4-3.8 bar inlet gauge pressure.
Inlet pressure (nominal) > 50 psi (345 kPa / 3.45 bar), peak inlet pressure at least 100 psi (690 kPa / 6.89 bar).
Pressure compensated design to give specified accuracy for whole range of input pressures
Built-in inlet filter.
Thorpe tube design flow meter using DISS input connector for panel /regulator mounting.
Can be cleaned with damp cloth and a disinfection solution.
Transparent, graduated (metric system) column, shatter resistant polymer certified for medical use.
Maximum flow rate when fully opened: 50 L/min.
Inlet and outlet connectors DISS style, other types of connectors available upon request
Adjustment knobs to have rough surface to prevent slipping.
Transparent, graduated (metric system) column, shatter resistant polymer certified for medical use.
Graduation shall have over 270 degrees of visibility.
Thorpe tube design flow meter using DISS input connector for panel /regulator mounting.
Pressure compensated design to give specified accuracy for whole range of input pressures
Built-in inlet filter (depending on supplied model).
Inlet and outlet connectors DISS style, other types of connectors available upon request
Can be cleaned with damp cloth and a disinfection solution.
Needle valve and body constructed of brass or aluminium.
Calibrated at 50-55 psi / 345-380 kPa / 3.4-3.8 bar inlet gauge pressure.
Inlet pressure (nominal) > 50 psi (345 kPa / 3.45 bar), peak inlet pressure at least 100 psi (690 kPa / 6.89 bar).
Maximum flow rate when fully opened: 50 L/min (depending on supplied model).
Medical gas flow meter (Thorpe tube design) to regulate and measure the flow rate of medical gas supplied to a patient, maximum flow rate 15 LPM, for medical oxygen.
Graduation shall have over 270 degrees of visibility.
Needle valve and body constructed of brass or aluminium.
Calibrated at 50-55 psi / 345-380 kPa / 3.4-3.8 bar inlet gauge pressure.
Inlet pressure (nominal) > 50 psi (345 kPa / 3.45 bar), peak inlet pressure at least 100 psi (690 kPa / 6.89 bar).
Pressure compensated design to give specified accuracy for whole range of input pressures
Thorpe tube design flow meter using DISS input connector for panel /regulator mounting.
Can be cleaned with damp cloth and a disinfection solution.
Transparent, graduated (metric system) column, shatter resistant polymer certified for medical use.
Built-in inlet filter (depending on supplied model).
Maximum flow rate when fully opened: 50 L/min (depending on supplied model).
Adjustment knobs to have rough surface to prevent slipping.
Inlet and outlet connectors DISS style, other types of connectors available upon request.
Medical gas flow meter (Thorpe tube design) to regulate and measure the flow rate of medical gas supplied to a patient, maximum flow rate 5 LPM, for medical medical air.
Graduation shall have over 270 degrees of visibility.
Needle valve and body constructed of brass or aluminium.
Pressure compensated design to give specified accuracy for whole range of input pressures.
Thorpe tube design flow meter using DISS input connector for panel /regulator mounting.
Can be cleaned with damp cloth and a disinfection solution.
Transparent, graduated (metric system) column, shatter resistant polymer certified for medical use.
Calibrated at 50-55 psi / 345-380 kPa / 3.4-3.8 bar inlet gauge pressure.
Inlet pressure (nominal) > 50 psi (345 kPa / 3.45 bar), peak inlet pressure at least 100 psi (690 kPa / 6.89 bar).
Medical gas flow meter (Thorpe tube design) to regulate and measure theflow rate of medical gas supplied to a patient, maximum flow rate 5 LPM,for medical oxygen.
Transparent, graduated (metric system) column, shatter resistant polymer certified for medical use.
Graduation shall have over 270 degrees of visibility.
Needle valve and body constructed of brass or aluminium.
Thorpe tube design flow meter using DISS input connector for panel /regulator mounting.
Can be cleaned with damp cloth and a disinfection solution.
Inlet and outlet connectors DISS style, other types of connectors available upon request
Adjustment knobs to have rough surface to prevent slipping.
Calibrated at 50-55 psi / 345-380 kPa / 3.4-3.8 bar inlet gauge pressure.
Inlet pressure (nominal) > 50 psi (345 kPa / 3.45 bar), peak inlet pressure at least 100 psi (690 kPa / 6.89 bar).
Pressure compensated design to give specified accuracy for whole range of input pressures.
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.
Provides a continuous, variable flow of concentrated oxygen 93% (±3%) derived from room air, to a maximum rate 8 L/min.
Equipped with a single oxygen outlet provided with controllable flowmeter.
Audible and/or visual alarms for low oxygen concentration (<82%) and power supply failure.
Contains oxygen monitor to verify concentration.
Flowmeter minimum flow rate of 2 L/min. Lower flow rates may be achieved by a combination of the concentrator and a separately supplied flow splitter (details under RELATED PRODUCTS).
Audible and visual alarms for high temperature and pressure failure.
Power efficiency ≤ 70 W/LPM.
Digital meter that displays cumulative hours of device operation.
Oxygen outlet(s) with 6 mm (¼-inch) barbed fitting.
Flowmeter continuously adjustable, with markings of at most 0.5 LPM intervals.
Noise level <60 dB(A).
CASING AND ENVIRONMENT
Oxygen outlet to be securely mounted and sheltered.
The unit includes internally and externally mounted filters for cleaning the air intake.
All user-removable filters are cleanable. Cleaning instructions for filters are included in the instructions for use.
Case to be hard, to be cleanable with standard hospital cleaning materials.
Whole unit to be movable with four wheels.
ELECTRICAL CHARACTERISTICS
Electrical power requirements to be locally compatible.
Capacity for safe operation from at least ± 10% of rated voltage.
Electrical protection by resettable circuit breakers or replaceable fuses.
230 Volt, 50 Hz, 2.1 amps (110 Volt units available upon request)
Mains power cable to have length ≥ 2.5 m.
An electrically-powered device designed to deliver high-flow (exceeding peak inspiratory flow) heated and humidified ambient air or air/oxygen to a neonatal patient as part of noninvasive ventilation (NIV); it may additionally be used with a water tank to produce bubble continuous positive airway pressure (bubble CPAP).
Continuous Positive Airway Pressure (Bubble CPAP) system for the non-invasive respiratory support of normal, premature or low-birth weight neonate with spontaneous breathing. The unit has an integrated pulseoximeter to measure the level of arterial oxygen saturation in blood.
It consists of a gas flow generator that entrains room air, an oxygen input, a heating element, and humidification chamber; it does not include CPAP controlling pressure sensors (i.e., not a full CPAP unit). It is intended for use by a healthcare provider on a spontaneously breathing patient in hospital settings.
A tool to measure the intensity and frequency spectrum of light sources used for the treatment of hyperbilirubinemia. Irradiance meter to measure the output of blue light phototherapy units for treatment of jaundice.
Suitable for conventional CFL (fluorescent), halogen blue light sources.
Suitable for fibreoptic, and LED light sources.
Designed for frequent disinfection with hospital-grade products.
Portable, handheld model.
Results are available within 5 seconds after commencement of the measurement.
Two models available, one model requires 2 x AAA alkaline batteries, another model has a built-in rechargeable lithium-ion battery.
The sensitivity is equal to or better than: 0.1 µW/cm²/nm.
Automatic zero adjustment at instrument switch-on.
Full batteries allow for 8 hours continues operation for the rechargeable version and 120 hours for the version with 2 x AAA alkaline batteries.
The spectral range for blue light is equal to or better than: 400 – 500 nm.
The spectral irradiance (in wavelength) range is equal to or better than: 0.1 – 150 µW/cm²/nm.
The unit has the following minimal features:
A self-check function.
LCD display clearly visualizing measurement results and other information.
Out of measurement range indicator.
Alarms for detector and/or system failure.
Low battery indicator.
An auto switch-off feature.
Portable suction machine for airway aspiration, minor surgery, emergency, patient transfer, suitable for use in hospitals and at home.
The unit provides intermediate and continuous suction. Continuous is limited to 30 minutes after which the unit should be given 30 minutes to cool down.
The flow rate at maximum vacuum is ≥ 33 L/m (2 m³/h).
The unit is provided with a suction tube of at least 1.5 meters.
The suction tube is made of medical grade silicone which is autoclavable at 121°C.
During operating the unit's noise level does not exceed 65.5 dB.
The unit is designed in such a way that it requires little or no oil.
The pump is equipped with a provision preventing fluid flowing to the pump if the collection jar is full (overflow control valve).
The unit is provided with one (1) reusable collection jar.
The unit has maintenance free operating.
A gauge indicating the negative pressure generated by the unit.
A hydrophobic bacterial filter is included in the airline to the pump.
The user adjustable suction ranges between 0 and at least 525 mmHg (70 kPa).
The unit should be provided with a carrying handle and storage provisions for all accessories, allowing to carry the unit with one hand.
The body is to be constructed of stainless steel or material which is non-corrosive or has a corrosion resistant coating.
The unit is equipped with a lead-acid battery.
The battery should be able to power the unit for up to 60 min.
The design of the device should be such that it is easy to clean/disinfect by avoiding difficult-to-reach areas and having smooth surfaces.
The device should have a sturdy, shock resistant casing.
A visual alarm should be incorporated in the unit signalling depletion of the batteries.
The unit should be provided with a battery level indicator and a charging indicator.
The unit should be able to simultaneously operate and charge from 12 Volt as well as the main power grid.
Power requirements: 230 Volts - 50Hz
The weight of the unit does not exceed 5.5 kg.
A reusable, hand-held, manual suction device designed to suck gently and clear excessive mucus from the airway of a newborn to facilitate easier breathing.
Reusable
Material: silicone
Can be autoclaved at 136°C and withstand other means of High Level Disinfection
Fully made from transparent or translucent material
No use of natural rubber latex
Fluid capacity: 75 ml
Can be disassembled (opened up) for proper cleaning. After opening up it should be easy to access the internals of the bulb allowing for thorough cleaning.
Nozzle dimensions at tip: Inner diameter (ID) 3.0mm ±5%
Nozzle dimensions at tip: Outer diameter (OD) 4.5mm ±5%
Suction strength should reach: 100mmHg (136cm H2O).
STORAGE INSTRUCTIONS
Storage Humidity: 10% to 95% relative humidity (non-condensing)
Storage Temperature: -40°C to +70°C
The Rad-G sensor is only compatible with the Rad-G device.
Prior to using this sensor the user should read and understand the Operator’s Manual for the Rad-G device and the Directions for Use included with the reusable sensor.
The reusable sensors are indicated for noninvasive spot-checking of functional oxygen saturation of arterial hemoglobin (SpO2) and pulse rate (measured by an SpO2 sensor) for use with adult, pediatric, and infant patients during both no motion and motion conditions, and for patients who are well or poorly perfused in hospitals, hospital-type facilities, mobile, and home environments.
The Reusable Sensor is indicated for the continuous noninvasive monitoring of functional oxygen saturation of arterial hemoglobin (SpO2) and pulse rate (measured by an SpO2 sensor) for use with adult, pediatric, infant, and neonatal patients during both no motion and motion conditions and for patients who are well or poorly perfused in hospitals, hospital-type facilities, mobile, and home environments.
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Handheld, portable, rechargeable battery powered pulse oximeter, for the noninvasive spot-checking or continuous monitoring of patient oxygen saturation (SpO2), pulse rate and respiratory rate.
Pulse Rate detection range: 25 - 240 bpm.
Pulse Rate resolution: 1 bpm.
Pulse Rate accuracy: within ± 3 bpm (no motion, low perfusion), ± 5 bpm (motion) for all patients (infants, children, adults).
Respiratory rate range: 4 to 70 rpm
Respiratory rate resolution: 1 rpm
Respiratory rate accuracy (no motion, adults/paediatrics (> 2 years)): within ± 3 rpm A(RMS), ± 1 rpm mean error
(Note: device is indicated for spot-checking or continuous monitoring of Respiration Rate from the photoplethysmogram (RRp) of adult and pediatric patients (> 2 years) during no motion conditions).
Measurement:
SpO2 and pulse rate monitor, with plethysmography waveform, for infants, children and adults.
SpO2 detection includes the range: 70 - 100 %.
SpO2 resolution: 1 %.
SpO2 accuracy (in the range at least 70 - 100%): ± 2% (no motion, low perfusion), ± 3% (motion) for all patients (infants, children, adults).
Display:
Data display refresh rate: every 1 s
Display with main parameters: %SpO2, pulse rate, respiratory rate, signal quality, status messages, battery state indication.
Casing:
Enclosure protection IP22.
Case and reusable probe suitable for cleaning and disinfection with hospital-grade cleaning products.
Overall device and probe weight < 300 g.
Electrical characteristics:
Operated by rechargeable, non-replaceable Li-ion battery power supply.
External AC battery charger, plug style and voltage as per local supply.
Charger certified to IEC 60601-1.
Protection against defibrillator discharges.
Suitable for operating by mains power and by battery.
Automatic switch between battery and mains powered modes.
The display shows which power source is in use.
Running time on battery only ≥ 12 hours (24h at lowest screen brightness and beep tone turned off).
Features:
Suitable for detection in low perfusion conditions.
Design enables use in demanding environments, e.g. shock, vibration.
Automatic correction for movement and ambient light artefacts.
Audible and visual alarms for low saturation and high/low pulse rate, thresholds settable by user.
Audible and visual alarms for sensor error or disconnected, system errors, low battery.
Alarm override and temporary silencing function.
Capable of working with, and supplied with, adult, paediatric and neonatal reusable probes.
Handheld, portable, rechargeable battery powered pulse oximeter, displaying patient oxygen saturation (SpO2), pulse rate and respiratory rate in real time.
Features:
Suitable for detection in low perfusion conditions down to perfusion index of 0.1%.
Design enables use in demanding environments, e.g. shock, vibration
Automatic correction for movement and ambient light artefacts
Audible and visual alarms for sensor error or disconnected, system errors, low battery.
Measurement:
SpO2, pulse rate and respiratory rate monitor, for infants, children, adults.
SpO2 detection includes the range: 70 - 100 %.
SpO2 resolution: 1 %.
SpO2 accuracy (in the range at least 70 - 100%): ± 2% (no motion, low perfusion), ± 3% (motion) for all patients (infants, children and adults).
Pulse Rate detection includes the range: 25 - 240 bpm.
Pulse Rate resolution: 1 bpm.
Pulse Rate accuracy: within ± 3 bpm (no motion, low perfusion), ± 5 bpm (motion) for all patients (infants, children, adults).
Respiratory rate includes the range: 4 to 90 rpm.
Respiratory rate resolution: 1 rpm
Respiratory rate accuracy within ± 1 rpm in ideal conditions
Electrical characteristics:
Operated by rechargeable, non-replaceable Li-ion battery, power supply
External AC battery charger, plug style and voltage as per local supply.
Charger certified to IEC 60601-1.
Protection against defibrillator discharges.
Suitable for operation by battery and by mains power supply, if connected and/or recharging.
Automatic switch between battery and mains powered modes, when recharging or in mains power failure.
The display shows which power source is in use.
Running time on battery only ≥ 12 hours (24h at lowest screen brightness and beep tone turned off).
Automatic power-off after period of no use.
Display:
Data display refresh rate ≤ 1 s
Display with main parameters: %SpO2, pulse rate, respiratory rate, signal quality, status messages, battery state indication.
Patient age group input feature.
Display indicates high and normal respiratory rate count for inputted age.
Display indicates when SpO2 < 90% (hypoxaemia per WHO guidelines.)
Casing:
Enclosure protection IPX2.
Case and probe suitable for cleaning and disinfection with hospital-grade cleaning products.
Overall device and probe weight < 300 g.
Hand-operated in a vertical position; the inflatable bag is operated an upright position perpendicular to the body being ventilated.
The resuscitator is autoclavable between 121°C and 134°C.
The resuscitator has a provision which allows connection of oxygen tubing.
Portable, self-inflating, reusable.
The resuscitator is equipped with a non-rebreather valve.
Resuscitator is easy to disassemble, clean, disinfect, and reassemble.
The capacity of the self-inflating ventilation bag is between 220 ml.
The resuscitator is equipped with a pressure release (limiting) valve which safeguards against generating ventilation pressures over 45 cmH?O, while still allowing for an airway pressure of at least 30 cmH?O.
All parts manufactured from high-strength, long-life materials that require no special maintenance or storage conditions.
The resuscitator, all its components and accessories are free of natural rubber latex.
The pressure release valve should allow to be overridden by the user when higher pressures need to be generated in the airways.
When the pressure release valve is not overridden by the user, it should automatically return to its default position whereby it protects against excess pressures. Users should not be able to lock the pressure release valve in a permanent closed position whereby there is no longer a safeguard against excessive ventilation pressures.
Resuscitators are used for ventilation assistance in critical situations of respiratory distress or failure. It is considered essential equipment for health structures and emergency rescue team (to be available in emergency room, delivery room, operating theatre, intensive care unit, ambulance, etc.).
It is considered essential equipment for health structures and emergency rescue team (to be available in emergency room, delivery room, operating theatre, intensive care unit, ambulance, etc.). Resuscitators are used for ventilation assistance in critical situations of respiratory distress or failure. Resuscitator intended for full-term babies, preterm and low-weight infants up to 7 kg.
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It is considered essential equipment for health structures and emergency rescue team (to be available in emergency room, delivery room, operating theatre, intensive care unit, ambulance, etc.). Resuscitators are used for ventilation assistance in critical situations of respiratory distress or failure.
Hand-operated in a horizontal position.
Portable, self-inflating, reusable.
The resuscitator is equipped with a non-rebreather valve.
An oxygen reservoir bag should be included with a capacity between 600-2 ,600 ml.
Resuscitator can be fully disassembled, is easy to clean, disinfect, and reassemble.
The resuscitator is equipped with a pressure release (limiting) valve which safeguards against generating ventilation pressures over 45 cmH?O, while still allowing for an airway pressure of at least 30 cmH?O.
The resuscitator is autoclavable between 121°C and 134°C.
The capacity of the self-inflating ventilation bag is 500ml.
Ventilation can be done with ambient air or with oxygen.
The resuscitator has an inlet valve with a nipple for oxygen tubing.
All parts manufactured from high-strength, long-life materials that require no special maintenance or storage conditions.
The resuscitator, all its components and accessories are free of natural rubber latex.
The pressure release valve should allow to be overridden by the user when higher pressures need to be generated in the airways.
When the pressure release valve is not overridden by the user, it should either automatically return to its default position whereby it protects against excess pressures, or be clearly visible so there is no doubt as to its closed position, even during an emergencies. To ensure users are fully aware that the limiting valve is in closed position.
Hand-operated in a horizontal position.
Portable, self-inflating, reusable.
Ventilation can be done with ambient air or with oxygen.
The resuscitator has an inlet valve with a nipple for oxygen tubing.
The resuscitator is equipped with a non-rebreather valve.
An oxygen reservoir bag should be included with a capacity between 2 ,500-2,600ml.
Resuscitator can be fully disassembled, is easy to clean, disinfect, and reassemble.
All parts manufactured from high-strength, long-life materials that require no special maintenance or storage conditions.
The resuscitator, all its components and accessories are free of natural rubber latex.
The resuscitator is autoclavable between 121°C and 134°C.
The capacity of the self-inflating ventilation bag is 1,600ml.
Flexible nasal catheter with hole at distal end.
Oxygen and air/oxygen mixture compatibility.
Transparent tubing, suitable for low pressure gas supply.
Consists of connector, tubing and sponge at distal end.
Anti-kink tubing, non-permanent deformation if kinked or bent too tight.
Rubber or soft plastic tubing and catheter, semi-rigid and allowing freedom of movement, PVC certified for medical use, hardness > 60 Shore A.
8 Fr tubing, catheter length 40 cm.
The reusable sensors are indicated for spot-checking or continuous, non-invasive measurement of arterial oxygen saturation (SpO2) and pulse rate for use with adult patients in operating rooms, recovery rooms, intensive care units (ICUs) and wards.
Nellcor standard compatible sensor.
Design: Reusable, finger clip
Plug type: DB9 pin
Cable length: 3.0m
Patient weight: ≥40kg.
The reusable sensors are indicated for spot-checking or continuous, non-invasive measurement of arterial oxygen saturation (SpO2) and pulse rate for use with children in operating rooms, recovery rooms, intensive care units (ICUs) and wards.
Nellcor standard compatible sensor.
Design: Reusable, finger clip
Plug type: DB9 pin
Cable length: 3.0m
Patient weight: 10 - 40kg.
The reusable sensors are indicated for spot-checking or continuous, non-invasive measurement of arterial oxygen saturation (SpO2) and pulse rate for use with neonates in operating rooms, recovery rooms, intensive care units (ICUs) and wards.
Design: Reusable, Y-style with built-in wrap-around belt for use on big toe or thumb.
Nellcor standard compatible sensor.
Cable length: 3.0m
Plug type: DB9 pin
Patient weight: 3 - 20kg.
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.
Equipped with one oxygen outlet, provided with controllable flow meter.
Audible and visual alarms for low oxygen concentration (<82%) and power supply failure.
Provides a continuous, variable flow of concentrated oxygen (>82%) derived from room air, to a maximum rate 10 L/min.
Contains oxygen monitor to verify concentration.
Audible and visual alarms for high temperature, no flow rate and low/high pressure.
Power efficiency < 70 W/L/min.
Flowmeter continuously adjustable, with markings of at most 0.5 L/min intervals.
Flowmeter control allows shutting off flow (i.e. 0 L/min) by user.
Noise level <60 dB(A).
Digital meter that displays cumulative hours of device operation.
Flowmeter minimum flow rate of 2 L/min. Lower flow rates may be achieved by a combination of the concentrator and a separately supplied flow splitter.
Oxygen outlet(s) with 6 mm (¼-inch) barbed fitting and DISS connector.
Electrical characteristics
Capacity for safe operation from at least ± 10% of rated voltage.
Electrical protection by resettable circuit breakers, fitted in both neutral and live lines.
Electrical power requirements are locally compatible.
230 Volt, 50 Hz, 3.0 amps (120 Volt units available)
Mains power cable length > 2.5 m.
Casing and environment
Hard case, cleanable with standard hospital cleaning materials.
Whole unit movable with wheels on at least two feet
All user-removable filters are cleanable. Cleaning instructions for filters are included in the instructions for use.
The unit includes internally and externally mounted filters for cleaning the air intake.
Unit weight <27 kg.
OXYGEN PRODUCTION
Provides a continuous, variable flow of concentrated oxygen 93% (±3%) derived from room air, to a maximum rate 8 L/min.
Audible and visual alarms for high temperature and pressure failure.
Power efficiency ≤ 70 W/LPM.
Digital meter that displays cumulative hours of device operation.
Oxygen outlet(s) with 6 mm (¼-inch) barbed fitting.
Contains oxygen monitor to verify concentration.
Equipped with two oxygen outlets each provided with controllable flow meter.
Audible and/or visual alarms for low oxygen concentration (<82%) and power supply failure.
Flowmeter continuously adjustable, with markings of at most 0.5 LPM intervals.
Noise level <60 dB(A).
Flowmeter minimum flow rate of 2 L/min. Lower flow rates may be achieved by a combination of the concentrator and a separately supplied flow splitter.
ELECTRICAL CHARACTERISTICS
Mains power cable to have length ≥ 2.5 m.
Capacity for safe operation from at least ± 10% of rated voltage.
Electrical power requirements to be locally compatible.
230 Volt, 50 Hz, 2.1 amps (110 Volt units available)
Electrical protection by resettable circuit breakers or replaceable fuses.
CASING AND ENVIRONMENT
Case to be hard, to be cleanable with standard hospital cleaning materials.
All user-removable filters are cleanable. Cleaning instructions for filters are included in the instructions for use.
Oxygen outlet to be securely mounted and sheltered.
Whole unit to be movable with four wheels.
The unit includes internally and externally mounted filters for cleaning the air intake.
Provides a continuous, variable flow of concentrated oxygen (>82%) derived from room air, to a maximum rate of 5 L/min.
Contains oxygen monitor to verify concentration.
Digital meter that displays cumulative hours of device operation.
Oxygen outlet(s) with 6 mm (¼-inch) barbed fitting and DISS connector.
Flowmeter minimum flow rate of 1 L/min. Lower flow rates may be achieved by a combination of the concentrator and a separately supplied flowmeter stand (details under RELATED PRODUCTS).
Flowmeter continuously adjustable, with markings of at most 0.5 L/min intervals.
Equipped with one oxygen outlet, provided with controllable flowmeter.
Audible and visual alarms for low oxygen concentration (<82%) and power supply failure.
Audible and visual alarms for high temperature, no flow rate and low/high pressure.
Power efficiency < 70 W/L/min.
Noise level <50 dB(A).
Contains flow limiter to prevent overdrawing oxygen flow beyond rated maximum flow rate.
Casing and environment
The unit includes internally and externally mounted filters for cleaning the air intake.
All user-removable filters are cleanable. Cleaning instructions for filters are included in the instructions for use.
Hard case, cleanable with standard hospital cleaning materials.
Whole unit movable with wheels on at least two feet
Unit weight <27 kg
Electrical characteristics
Capacity for safe operation from at least ± 10% of rated voltage.
Electrical protection by resettable circuit breakers, fitted in both neutral and live lines.
Electrical power requirements are locally compatible.
230 Volt, 50 Hz, 3.0 amps (120 Volt units available)
Mains power cable length > 2.5 m.
Hand held, battery powered device that measures the oxygen concentration in a flow of gas from a medical gas source or, with adapters, through a medical gas-flow device such as a ventilator or anaesthesia system. The intended application is checking gas supply equipment performance.
Operational Characteristics:
Suitable for measuring gas supply with pressure up to 50 psi (344 kPa)
Response time < 20 s.
Warm-up time < 1 s.
Flow rate measurement: up to 10 LPM
Flow rate accuracy within ± 0.2 LPM
Flow rate resolution 0.1 LPM
Display visualizing O2 concentration, flow rate, system messages and battery status.
Ultrasonic oxygen sensing technology, with permanent sensing chamber.
O2 measurement to include the range 21 - 96%.
O2 accuracy: within ± 1.5% of full scale.
O2 resolution: 0.1%.
Handheld, battery powered device that measures the oxygen concentrationin a flow of gas from a medical gas source or, with adapters, through a medical gas-flow device such as a ventilator or anaesthesia system, or within an environment such as oxygen hood and infant incubator.
Operational characteristics:
Handheld oxygen analyzer for continuous measurement of the oxygen concentration from a medical gas source and in an environment.
Suitable for measuring gas supply with pressure up to 50 psi (344 kPa).
Response time: ≤ 20 s.
Electrochemical cell oxygen sensing technology.
O2 resolution: 0.1 %.
O2 measurement includes the range 0.0 - 100%.
O2 accuracy: within ± 3 %.
Warm-up time: none required
Display visualizing O2 concentration, system messages and battery status.
Internal calibration timer (weekly); alerts the operator, using a calibration icon on the LCD display, to perform a unit calibration one week after previous calibration.
Low and high oxygen concentration alarm system, with flashing LED and audible indication of alarm conditions.
Replaceable oxygen sensor cell, expected sensor life >1,500,000 O2% hours over 2 years in typical applications.
Calibration and self-test mode, one point calibration 20.9% or 100%.
An electrically powered device designed to deliver high-flow (exceeding peak inspiratory flow) heated and humidified ambient air or air/oxygen to a neonatal patient as part of non-invasive ventilation (NIV); it may additionally be used with a water tank to produce bubble continuous positive airway pressure (bubble CPAP). It is intended for use by a healthcare provider on a spontaneously breathing patient in hospital settings. It consists of a gas flow generator that entrains room air, an oxygen concentrator, a heating provision, and humidification chamber; it does not include CPAP controlling pressure sensors.
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