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Silicon Premium Full Face Mask – Vented

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Silicone Premium Full Face Mask is intended for use at Home or Hospital by patients on Pressure Support Ventilation.

Single Patient Use

TECHNICAL SPECIFICATIONS
Hospital Vented Full Face Mask HHFF3W-V HHFF4W-V HHFF5W-V
Resistance (50LPM) 0.70 cmH2O 0.69 cmH2O 0.65 cmH2O
Dead Space 283 ml 337 ml 341 ml
Pressure 4 cmH2O 13.6 L/min 13.6 L/min 13.8 L/min
Pressure 8 cmH2O 17 L/min 17.3 L/min
Pressure 12 cmH2O 19.1 L/min 20.7 L/min 21.8 L/min
Pressure 16 cmH2O 21.6 L/min 22.5 L/min 23.3 L/min
Pressure 20 cmH2O 26.4 L/min 26.2 L/min 27.1 L/min

Download PDF

 

STORAGE AND TRANSPORT
  • -15 C to +60 C (+5 F to +140 F)
  • 10% to 90% relative humidity non condensing.
  • Store the mask in a dry place away from direct sunlight.

SIZES
HHFF3W-V Vented Small
HHFF4W-V Vented Medium
HHFF5W-V Vented Large

Silicon Premium Full Face Mask – Non Vented

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Silicone Premium Full Face Mask is intended for use at Home or Hospital by patients on Pressure Support Ventilation.

Single Patient Use

TECHNICAL SPECIFICATIONS
Hospital Vented Full Face Mask HHFF3W-V HHFF4W-V HHFF5W-V
Resistance (50LPM) 0.70 cmH2O 0.69 cmH2O 0.65 cmH2O
Dead Space 283 ml 337 ml 341 ml

 

STORAGE AND TRANSPORT
  • -15 C to +60 C (+5 F to +140 F)
  • 10% to 90% relative humidity non condensing.
  • Store the mask in a dry place away from direct sunlight.

SIZES
HHFF3W-NV Non-vented Small
HHFF4W-NV Non-vented Medium
HHFF5W-NV Non-vented Large

 

MultiSteth

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ECG Monitor Interface
SpO2 Monitor Interface

 

Features

  • Regular stethoscope, ECG waveform display, heart and pulse oximeter (Optional) 08
  • Large LCD screen display:160 x 96;LED back light
  • RS232 interface connection to computer for charging the battery
  • Changeable Spo2 sensor (optional) for all patient ages
  • Freeze function: convenient to observe the hear rate, ECG or SPO2
  • Real-time display of the hear rate, ECG and Spo2
  • Low power consumption, Long life battery
  • Spo2 is optional

Specifications

  • Light weight : Weight only 200g
  • Operation : 40 hours approx
  • Auto switch off: 4 minutes if there is no data input
  • LCD Display: Pixel 160 x 96
  • Display Zone 60 x 34mm
  • ECG Waveform Rolling Speed:6.25mm/s 1.25mm/s 25mm/s
  • Sensitivity: Automatic
  • Heart Rate Accuracy: ±2 bpm
  • SpO2 Accuracy: When the range is 70%-100%, the permission of absolute error is ±2% below 70% unspecified
  • Pulse Rate Accuracy: ±2 bpm or ±2% (select larger)

Nasal Cannula

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  • Made of medical PVC

  • Two tips, over ear style

  • Anti-crush 7ft,PVC tubing

  • The length of tube could be at customer’s request

  • Specially designed accessory to use with oxygen
    concentrator or similar Oxygen source

  
Download PDF

 

PRODUCT SPECIFICATIONS

CODE DESCRIPTION
C0201 Adult,standard tip C0202 Pediatric,standard tip
C0203 Infant,standard tip C0204 Adult,flared tip
C0205 Adult,soft tip C0206 Pediatric,soft tip
C0207 Infant,soft tip C0208 Neonatal,soft tip
C0209 Adult, curved tip

Aeroneb GO Micropump Nebuliser

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The Aeroneb® Go nebuliser is a fast, efficient, simple-to-use nebuliser developed for the millions of patients worldwide who require respiratory therapy in and away from home.

The Aeroneb Go can be used by paediatric as well as adult patients and is ideal for conditions such as asthma and chronic obstructive pulmonary disease (COPD). The Aeroneb Go aerosolises clinician-prescribed solutions for inhalation that are approved for use with a general purpose nebuliser.

Designed with convenience in mind and to help users maintain normal daily schedules, it is ultra-lightweight, portable, silent and is hassle free to set up and operate.

SPECIFICATIONS
Weight Nebuliser Unit 60g
Sound level <35dBA at 1 metre
Medication cup capacity 6ml
Residual volume Typically <0.3ml
Average flow rate 0.4ml/min
Average particle size 3.6μm MMAD

TWO POWER OPTIONS
  1. AC/DC

Powered

2. 3 AA Batteries

Aeroneb PRO In - Line Nebuliser

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Introducing the Aeroneb® Professional Nebulizer System

An exceptional aerosol delivery option for clinicians that saves time, lowers costs and provides flexibility for respiratory therapy throughout the hospital.

The Aeroneb Pro provides effective dose delivery of physicianprescribed inhalation solutions for infants through adults requiring positive pressure breathing assistance, including mechanicalventilation, as well as hand-held nebulizer therapy. Utilizing Aerogen’s OnQ™ Aerosol Generator, the Aeroneb Pro produces a fine particle, low velocity aerosol without environmentally unfriendly propellants, inefficient compressors or costly ultrasonic elements.

The Aeroneb Pro overcomes the issue of poor aerosol delivery during mechanical ventilation, depositing up to four times more medication through an endotracheal tube (in vitro) during mechanical ventilation than small volume nebulizers (SVNs). SVNs have been reported to deliver between 1–3%1 of the nominal dose to the lungs during mechanical ventilation, compared to 2–18%2 in nonintubated patients.
Efficient
  • Saves time
  • Does not affect ventilator parameters
  • during operation or refill
  • Maximizes respirable dose with 2.1 μm average MMAD,low residual volume and minimal rainout
  • Does not collect or nebulize condensate from ventilatorcircuit during operation
  • Unique aerosol generator does not heat or degrademedications
Flexible
  • Operates inline or independently for
    infants through adults
  • Delivers all medications approved for use with standardnebulizers to treat infants through adults
  • Operates inline with standard ventilator circuits andmechanical ventilators
  • Usable in the hospital, ambulatory clinics and duringpatient transport
  • Lightweight control module powered by AC orrechargeable battery
Cost-Effective
  • Reduces cost
  • Low residual volume minimizes drug waste
  • Multiple patient use
  • Low residual volume in medication cup (average 0.3 mLof 3 mL dose) minimizes drug waste
  • Multiple patient use
  • Autoclavable at 132ºC – 135ºC (270ºF – 275ºF)

 

PRODUCT SPECIFICATIONS

Physical Nebulizer Unit weight: 25 grams (0.9 oz.)

Control Module weight: 230 grams (8.1 oz.)

Medication cup capacity: 10 mL
Power Consumption: <6.5 watts (charging), <2.0 watts (nebulizing)

AC/DC adapter (input 100 to 240 VAC 50/60Hz, output 9 V)

or rechargeable battery (4.8 V nominal output)

Patient isolation: Approved to IEC 60601-1 and AAMI ES1
Performance See Performance Characteristics Table

Noise level: Silent operation

Frequency, Nebulizer Unit: 128 kilohertz (kHz)
Configuration Options
 

ORDER SPECIFICATIONS

Aeroneb® Professional Nebulizer System AG-AP6000
Aeroneb® Professional (autoclavable) Nebulizer Unit AG-AP1000
Accessories and replacement parts available. For more product
information, visit Aerogen’s website at www.aerogen.com

Curasa Auto CPAP

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Curasa Auto works in sync with the patient to reduce Work of Breathing (WOB) using Adaptive Triggering Technology (ATT).

These machines are extremely lightweight compact, and aesthetic looking. They are ideal for home use or during travel.

The New Cutting Edge Technology incorporates the measurement of the CPAP pressure directly at the mask level through a specially designed Hose Pipe.

This technology makes it possible for accurate leak management and completely avoids adjustment for compensation for altitude, Leak and external devices such as Humidifiers in the patient’s circuit.

One of the main reasons for machine fault is the seepage of water from the integrated humidifier into the machine during transport or shifting. In Curasa Nasal CPAP systems, the disconnection of the integrated humidifier connecting pipe isolates the flow generator from the humidifier.
Curasa Auto algorithm dynamically responds to Apnea, Hypopnea, Flow Limitation, Snoring, Obstructive Apnea and Mouth Leak.

Curasa Specifications

Pressure Range 4cmH20 – 20cmH20
Pressure Variance / Control ±0.4cmH20
Ramp Time 0-60min adjustable 1min/step
Noise (10cm H2O / ~1.0KPa) <29dB (A)
Dimensions 170mm x 117mm x 93mm
Weight 1.05kg (1.4Kg with Humidifier)
Automatic Altitude Compensation 700hPa ~ 1060hPa
Mask On / Off Detection Automatic Start/Stop on breath detection
Alarms Power Faliure
Power Supply 100-240VAC, 50/60 Hz, 24DV, 2.5 A max.
Compliance Meter 1st on operation, 2nd on breath detection
Protection against shock / Water ingress Class II, Type B applied part / IPXO
Electromagnetic compatibility EN 60601-1-2
CE Certification CE 0123
Pressure Control At the Patient Mask
Operational relative Humidity 10% ~ 93% (Non-condensing)
Humidifier Integrated, 250ml, 44 C
Curasa Auto Responds to Apnea, Hpopnea, Flow Limitation, snoring,
leak, mouth opening, over 365 nights data
storage, Auto Manager Software
(USB Connectivity)

Floton ST33 Advanced Non-Invasive Ventilation

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Adaptive Triggering Technology (ATT) tracks every breath and monitors the different stages of the respiration cycle utilizing an Advanced Leak Calculation Algorithm that ensures reduced work of breathing (WOB) whilst providing the patient with effective and comfortable treatment.

Curative Medical Inc., USA introduces new Floton Non-Invasive Bi Level Positive Airway Pressure systems for the treatment of Respiratory insufficiency including COPD and Obstructive Sleep Apnea.

Compact, Lightweight and Quiet the Floton BiLevel Series understands that every breath is different using the Advanced Adaptive Triggering Technology (ATT) designed to effortlessly synchronize with the natural breathing of the patient.

The New Cutting Edge Technology incorporates the measurement of the pressure directly at the mask level through a specially designed Hose Pipe.
This technology makes it possible for accurate leak management and enhances the sensitivity of the machine to detect extremely low patient effort.Floton ST series ventilators have advanced modes of BiLevel Ventilation including CPAP, S, ST, T, APCV. The new APCV (Assisted Pressure Control Ventilation) mode allows the patient to trigger an inspiration even as it follows the Time cycle and backup breath rate decided by the physician.One of the main reasons for machine fault is the seepage of water from the integrated humidifier into the machine during transport or shifting. In Floton BiLevel Systems, the disconnection of the integrated humidifier connecting pipe isolates the flow generator from the humidifier.

 

Floton Specifications

Pressure Range ST33 : 4cmH20 – 33cmH20
Pressure Measurement Mask Pressure
Ramp Time 0-60min adjustable 1min/step
BPM* 5 to 50 Breaths Per Minute
I/E%* 10% to 80%
Ventilation Mode* 5 modes: S, T *, ST *, APCV * and CPAP
I-Slop 6 levels. From 100msec to 600msec
Expiratory Cycling E-Sens : 6 Levels
Inspiration Triggering I-Sens : 6 Levels, Adaptive Triggering /
Technology (ATT)
Tidal Volume 50 to 3000ml
Noise (10cm H2O ) <28dB (A)
Dimensions 180mm x 210mm x 105mm
Weight 1.2kg (1.55kg with humidifier)
Automatic Altitude Compensation 700hPa ~ 1060hPa
Mask On / Off Detection Automatic Start/Stop on breath detection
Alarms Power Failure, Low minute ventilation,Low Tidal Volume, Apnea, High Pressure
Power Supply 100-240 VAC, 50/60 Hz, 24DV, 2.5 A max.
Protection against shock / Water ingress Class II, Type B applied part / IPXO
Electromagnetic compatibility EN 60601-1-2
Certification CE 0123
Relative Humidity 10% ~ 93% (Non-condensing)
Humidifier** Heated, Integrated, 250ml, 44 C
Data Recording 365 days of data storage, Respiratory Events,
Trends of Pressure leak and Respiratory Rate.
* : Feature not available in Floton S20** : Humidifier Optional

Floton ST25 Advanced Non-Invasive Ventilation

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Adaptive Triggering Technology (ATT) tracks every breath and monitors the different stages of the respiration cycle utilizing an Advanced Leak Calculation Algorithm that ensures reduced work of breathing (WOB) whilst providing the patient with effective and comfortable treatment.

Curative Medical Inc., USA introduces new Floton Non-Invasive Bi Level Positive Airway Pressure systems for the treatment of Respiratory insufficiency including COPD and Obstructive Sleep Apnea.

Compact, Lightweight and Quiet the Floton BiLevel Series understands that every breath is different using the Advanced Adaptive Triggering Technology (ATT) designed to effortlessly synchronize with the natural breathing of the patient.

The New Cutting Edge Technology incorporates the measurement of the pressure directly at the mask level through a specially designed Hose Pipe.
This technology makes it possible for accurate leak management and enhances the sensitivity of the machine to detect extremely low patient effort.Floton ST series ventilators have advanced modes of BiLevel Ventilation including CPAP, S, ST, T, APCV. The new APCV (Assisted Pressure Control Ventilation) mode allows the patient to trigger an inspiration even as it follows the Time cycle and backup breath rate decided by the physician.One of the main reasons for machine fault is the seepage of water from the integrated humidifier into the machine during transport or shifting. In Floton BiLevel Systems, the disconnection of the integrated humidifier connecting pipe isolates the flow generator from the humidifier.

 

Floton Specifications

Pressure Range ST25 : 4cmH20 – 25cmH20
Pressure Measurement Mask Pressure
Ramp Time 0-60min adjustable 1min/step
BPM* 5 to 50 Breaths Per Minute
I/E%* 10% to 80%
Ventilation Mode* 5 modes: S, T *, ST *, APCV * and CPAP
I-Slop 6 levels. From 100msec to 600msec
Expiratory Cycling E-Sens : 6 Levels
Inspiration Triggering I-Sens : 6 Levels, Adaptive Triggering /
Technology (ATT)
Tidal Volume 50 to 3000ml
Noise (10cm H2O ) <28dB (A)
Dimensions 180mm x 210mm x 105mm
Weight 1.2kg (1.55kg with humidifier)
Automatic Altitude Compensation 700hPa ~ 1060hPa
Mask On / Off Detection Automatic Start/Stop on breath detection
Alarms Power Failure, Low minute ventilation,Low Tidal Volume, Apnea, High Pressure
Power Supply 100-240 VAC, 50/60 Hz, 24DV, 2.5 A max.
Protection against shock / Water ingress Class II, Type B applied part / IPXO
Electromagnetic compatibility EN 60601-1-2
Certification CE 0123
Relative Humidity 10% ~ 93% (Non-condensing)
Humidifier** Heated, Integrated, 250ml, 44 C
Data Recording 365 days of data storage, Respiratory Events,
Trends of Pressure leak and Respiratory Rate.
* : Feature not available in Floton S20** : Humidifier Optional

Floton ST20 Advanced Non-Invasive Ventilation

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Adaptive Triggering Technology (ATT) tracks every breath and monitors the different stages of the respiration cycle utilizing an Advanced Leak Calculation Algorithm that ensures reduced work of breathing (WOB) whilst providing the patient with effective and comfortable treatment.

Curative Medical Inc., USA introduces new Floton Non-Invasive Bi Level Positive Airway Pressure systems for the treatment of Respiratory insufficiency including COPD and Obstructive Sleep Apnea.

Compact, Lightweight and Quiet the Floton BiLevel Series understands that every breath is different using the Advanced Adaptive Triggering Technology (ATT) designed to effortlessly synchronize with the natural breathing of the patient.

The New Cutting Edge Technology incorporates the measurement of the pressure directly at the mask level through a specially designed Hose Pipe.
This technology makes it possible for accurate leak management and enhances the sensitivity of the machine to detect extremely low patient effort.

Floton ST series ventilators have advanced modes of BiLevel Ventilation including CPAP, S, ST, T, APCV. The new APCV (Assisted Pressure Control Ventilation) mode allows the patient to trigger an inspiration even as it follows the Time cycle and backup breath rate decided by the physician.

One of the main reasons for machine fault is the seepage of water from the integrated humidifier into the machine during transport or shifting. In Floton BiLevel Systems, the disconnection of the integrated humidifier connecting pipe isolates the flow generator from the humidifier.

 

Floton Specifications

Pressure Range BiLevel – ST20 : 4cmH20 – 20cmH20
Pressure Measurement Mask Pressure
Ramp Time 0-60min adjustable 1min/step
BPM* 5 to 50 Breaths Per Minute
I/E%* 10% to 80%
Ventilation Mode* 5 modes: S, T *, ST *, APCV * and CPAP
I-Slop 6 levels. From 100msec to 600msec
Expiratory Cycling E-Sens : 6 Levels
Inspiration Triggering I-Sens : 6 Levels, Adaptive Triggering /
Technology (ATT)
Tidal Volume 50 to 3000ml
Noise (10cm H2O )

 <28dB (A)
Dimensions 180mm x 210mm x 105mm
Weight 1.2kg (1.55kg with humidifier)
Automatic Altitude Compensation 700hPa ~ 1060hPa
Mask On / Off Detection Automatic Start/Stop on breath detection
Alarms

 

 Power Failure, Low minute ventilation,

Low Tidal Volume, Apnea, High Pressure
Power Supply 100-240 VAC, 50/60 Hz, 24DV, 2.5 A max.
Protection against shock / Water ingress Class II, Type B applied part / IPXO
Electromagnetic compatibility EN 60601-1-2
Certification CE 0123
Relative Humidity 10% ~ 93% (Non-condensing)
Humidifier** Heated, Integrated, 250ml, 44 C
Data Recording 365 days of data storage, Respiratory Events,
Trends of Pressure leak and Respiratory Rate.
* : Feature not available in Floton S20

** : Humidifier Optional

YH1000 Polymate

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PneumoCare YH-1000 is a brand new intelligent diagnosis system, suitable for clinic study and screening of Sleep Apnea Syndrome (SAS).

Multiple Function

- 11 channels: SpO2, Pulse rate, Airflow, Respiratory drive (2-CH), Snoring, Body position, CPAP pressure, Patient event, Battery, Recording time

- Compliant with the level III of international sleep diagnosis standard

 

Excellent Ergonomic design

- Small size, light weight and low electricity consumption

- 3.1 inches LCD displays all parameters and waves in real time

- Automatic on/off setting

Friendly design

- Record more than 12 hours overnight data

- Display recording time in real time

- Left battery energy is displayed automatically.

- Keep up recording from the pause point for the data integrity

 

Efficiency and flexibility

- Easy operation, accurate result, meeting the requirement of Sleep Apnea diagnosis

- CPAP titration

 

Powerful software and concise report

- Analysis software includes sleep-awake distribution, breathing disorder analysis, Oxygen saturation reduction and CPAP pressure histogram etc.

- Abundant reporting can be customized printed.

 

Technical Specifications:

Channels SpO2, Pulse rate, Airflow, Respiratory drive (2-CH), Snoring, Body position, CPAP pressure, Patient event, Battery, Recording time
Screen 3.1 inches LCD with backlit
Display SpO2, Pulse rate, Airflow, Respiratory drive (2-CH), Snoring, Body position, Battery, Date and time
Language English and French
Memory > 12 hours data
Dimensions 139mm (L) X 82mm (W) X 37mm (H)
Weight 350g
Power Supply DC 3V (2 X R6 AA)

Curasa CPAP

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Curasa CPAP Provides continuous Positive Airway Pressure to the Patient.Curative  Medical  inc., USA  introduces  new Curasa  Nasal  CPAP Therapy systems for the treatment of Obstructive Sleep Apnea. Curasa    CPAP    systems     are    medical devices   for   providing   highly efficient CPAP pressure   to   patients  over a very wide range of pressures.

These machines are extremely lightweight compact, and  aesthetic  looking. They are ideal for home use or during travel. The New Cutting Edge Technology  incorporates  the  measurement of the CPAP pressure directly at the mask level through a specially designed Hose Pipe.

This technology makes it possible for accurate leak  management   and   completely   avoids adjustment   for   compensation for altitude, Leak and external devices such as Humidifiers in the patient’s circuit.

One of the main reasons for machine fault is the seepage of water from the integrated humidifier into the machine during transport or shifting. In Curasa Nasal CPAP systems, the disconnection  of   the  integrated humidifier connecting   pipe  isolates the flow generator from  the humidifier.

CURASA Specifications

Pressure Range 4cmH20 – 20cmH20
Pressure Variance / Control ±0.4cmH20
Ramp Time 0-60min adjustable 1min/step
Noise (10cm H2O / ~1.0KPa) <29dB (A)
Dimensions 170mm x 117mm x 93mm
Weight 1.05kg (1.4Kg with Humidifier)
Automatic Altitude Compensation 700hPa ~ 1060hPa
Mask On / Off Detection Automatic Start/Stop on breath detection
Alarms Power Faliure
Power Supply 100-240VAC, 50/60 Hz, 24DV, 2.5 A max.
Compliance Meter 1st on operation, 2nd on breath detection
Protection against shock / Water ingress Class II, Type B applied part / IPXO
Electromagnetic compatibility EN 60601-1-2
CE Certification CE 0123
Pressure Control At the Patient Mask
Operational relative Humidity 10% ~ 93% (Non-condensing)
Humidifier Integrated, 250ml, 44 C
Curasa EUT 3 levels
Curasa Auto Apneas, Hpopnea, Flow Limitation, snoring,
leak, mouth opening, over 365 nights data
storage, Auto Manager Software
(USB Connectivity)